Ignite Creation Date:
2025-12-25 @ 3:13 AM
Ignite Modification Date:
2025-12-26 @ 1:52 AM
Study NCT ID:
NCT05345405
Status:
COMPLETED
Last Update Posted:
2025-06-08
First Post:
2022-04-06
Is NOT Gene Therapy:
False
Has Adverse Events:
True
Brief Title:
Clinical Trial of a Supporter-Targeted Intervention to Improve Outcomes in Recent Sexual Assault Survivors
Sponsor:
Organization:
Raw JSON
{'hasResults': True, 'derivedSection': {'miscInfoModule': {'versionHolder': '2025-12-24'}, 'conditionBrowseModule': {'meshes': [{'id': 'D013313', 'term': 'Stress Disorders, Post-Traumatic'}, {'id': 'D006379', 'term': 'Helping Behavior'}, {'id': 'D000066505', 'term': 'Help-Seeking Behavior'}], 'ancestors': [{'id': 'D040921', 'term': 'Stress Disorders, Traumatic'}, {'id': 'D000068099', 'term': 'Trauma and Stressor Related Disorders'}, {'id': 'D001523', 'term': 'Mental Disorders'}, {'id': 'D012919', 'term': 'Social Behavior'}, {'id': 'D001519', 'term': 'Behavior'}]}}, 'resultsSection': {'moreInfoModule': {'pointOfContact': {'email': 'edworkin@uw.edu', 'phone': '206-503-3287', 'title': 'Principal Investigator', 'organization': 'University of Washington'}, 'certainAgreement': {'piSponsorEmployee': False, 'restrictiveAgreement': False}}, 'adverseEventsModule': {'timeFrame': 'From enrollment until end of follow-up, up to 3 months', 'eventGroups': [{'id': 'EG000', 'title': 'Dyadic CARE (Survivors)', 'description': 'Survivors randomized to receive dyadic CARE (both dyad members attended both sessions and completed a workbook together)', 'otherNumAtRisk': 21, 'deathsNumAtRisk': 21, 'otherNumAffected': 0, 'seriousNumAtRisk': 21, 'deathsNumAffected': 0, 'seriousNumAffected': 0}, {'id': 'EG001', 'title': 'Supporter-Only CARE (Survivors)', 'description': 'Survivors randomized to receive supporter-only CARE (only the supporter attended both sessions; the dyad completed a workbook together)', 'otherNumAtRisk': 21, 'deathsNumAtRisk': 21, 'otherNumAffected': 0, 'seriousNumAtRisk': 21, 'deathsNumAffected': 0, 'seriousNumAffected': 0}, {'id': 'EG002', 'title': 'Waitlist Control (Survivors)', 'description': 'Survivors randomized to receive waitlist CARE (invited to complete the CARE version of their choice following the completion of study measures)', 'otherNumAtRisk': 21, 'deathsNumAtRisk': 21, 'otherNumAffected': 0, 'seriousNumAtRisk': 21, 'deathsNumAffected': 0, 'seriousNumAffected': 0}, {'id': 'EG003', 'title': 'Dyadic CARE (Supporters)', 'description': 'Supporters randomized to receive dyadic CARE (both dyad members attended both sessions and completed a workbook together)', 'otherNumAtRisk': 21, 'deathsNumAtRisk': 21, 'otherNumAffected': 0, 'seriousNumAtRisk': 21, 'deathsNumAffected': 0, 'seriousNumAffected': 0}, {'id': 'EG004', 'title': 'Supporter-Only CARE (Supporters)', 'description': 'Supporters randomized to receive supporter-only CARE (only the supporter attended both sessions; the dyad completed a workbook together)', 'otherNumAtRisk': 21, 'deathsNumAtRisk': 21, 'otherNumAffected': 0, 'seriousNumAtRisk': 21, 'deathsNumAffected': 0, 'seriousNumAffected': 0}, {'id': 'EG005', 'title': 'Waitlist Control (Supporters)', 'description': "Supporters randomized to receive waitlist CARE (invited to complete the CARE version of the survivor's choice following the completion of study measures)", 'otherNumAtRisk': 21, 'deathsNumAtRisk': 21, 'otherNumAffected': 0, 'seriousNumAtRisk': 21, 'deathsNumAffected': 0, 'seriousNumAffected': 0}], 'frequencyThreshold': '0'}, 'outcomeMeasuresModule': {'outcomeMeasures': [{'type': 'PRIMARY', 'title': 'Survivor Satisfaction With Intervention at 1 Month Post-baseline (Self Report)', 'denoms': [{'units': 'Participants', 'counts': [{'value': '19', 'groupId': 'OG000'}, {'value': '21', 'groupId': 'OG001'}]}], 'groups': [{'id': 'OG000', 'title': 'Dyadic CARE (Survivors)', 'description': 'Survivors randomized to receive dyadic CARE (both dyad members attended both sessions and completed a workbook together)'}, {'id': 'OG001', 'title': 'Supporter-Only CARE (Survivors)', 'description': 'Survivors randomized to receive supporter-only CARE (only the supporter attended both sessions; the dyad completed a workbook together)'}], 'classes': [{'categories': [{'measurements': [{'value': '28.37', 'spread': '3.39', 'groupId': 'OG000'}, {'value': '27.71', 'spread': '3.51', 'groupId': 'OG001'}]}]}], 'paramType': 'MEAN', 'timeFrame': '1 month', 'description': 'Sum score on Client Satisfaction Scale, completed by survivor. Range: 8 to 32; higher scores indicate greater satisfaction', 'unitOfMeasure': 'score on a scale', 'dispersionType': 'Standard Deviation', 'reportingStatus': 'POSTED', 'populationDescription': '2 participants did not complete this scale.'}, {'type': 'PRIMARY', 'title': 'Supporter Satisfaction With Intervention at 1 Month Post-baseline (Self Report)', 'denoms': [{'units': 'Participants', 'counts': [{'value': '20', 'groupId': 'OG000'}, {'value': '20', 'groupId': 'OG001'}]}], 'groups': [{'id': 'OG000', 'title': 'Dyadic CARE (Supporters)', 'description': 'Supporters randomized to receive dyadic CARE (both dyad members attended both sessions and completed a workbook together)'}, {'id': 'OG001', 'title': 'Supporter-Only CARE (Supporters)', 'description': 'Supporters randomized to receive supporter-only CARE (only the supporter attended both sessions; the dyad completed a workbook together)'}], 'classes': [{'categories': [{'measurements': [{'value': '29.79', 'spread': '2.65', 'groupId': 'OG000'}, {'value': '29.60', 'spread': '2.28', 'groupId': 'OG001'}]}]}], 'paramType': 'MEAN', 'timeFrame': '1 month', 'description': 'Sum score on Client Satisfaction Scale, completed by supporter. Range: 8 to 32; higher scores indicate greater satisfaction', 'unitOfMeasure': 'score on a scale', 'dispersionType': 'Standard Deviation', 'reportingStatus': 'POSTED', 'populationDescription': '2 participants did not complete this scale.'}, {'type': 'PRIMARY', 'title': 'Change in Survivor Knowledge at 1 Month Post-baseline (Self Report)', 'denoms': [{'units': 'Participants', 'counts': [{'value': '17', 'groupId': 'OG000'}, {'value': '20', 'groupId': 'OG001'}, {'value': '20', 'groupId': 'OG002'}]}], 'groups': [{'id': 'OG000', 'title': 'Dyadic CARE (Survivors)', 'description': 'Survivors randomized to receive dyadic CARE (both dyad members attended both sessions and completed a workbook together)'}, {'id': 'OG001', 'title': 'Supporter-Only CARE (Survivors)', 'description': 'Survivors randomized to receive supporter-only CARE (only the supporter attended both sessions; the dyad completed a workbook together)'}, {'id': 'OG002', 'title': 'Waitlist Control (Survivors)', 'description': 'Survivors randomized to receive waitlist CARE (invited to complete the CARE version of their choice following the completion of study measures)'}], 'classes': [{'categories': [{'measurements': [{'value': '3.24', 'spread': '3.70', 'groupId': 'OG000'}, {'value': '0.20', 'spread': '3.47', 'groupId': 'OG001'}, {'value': '0.61', 'spread': '4.75', 'groupId': 'OG002'}]}]}], 'paramType': 'MEAN', 'timeFrame': 'Baseline, 1 month', 'description': 'Sum score on a knowledge questionnaire reflecting CARE concepts, completed by the survivor. Range: 8 to 40; higher scores indicate more knowledge about CARE concepts.', 'unitOfMeasure': 'score on a scale', 'dispersionType': 'Standard Deviation', 'reportingStatus': 'POSTED', 'populationDescription': 'Because this is a change score, participants were excluded listwise if they had missing data at one or both assessments.'}, {'type': 'PRIMARY', 'title': 'Change in Supporter Knowledge at 1 Month Post-baseline (Self Report)', 'denoms': [{'units': 'Participants', 'counts': [{'value': '18', 'groupId': 'OG000'}, {'value': '19', 'groupId': 'OG001'}, {'value': '18', 'groupId': 'OG002'}]}], 'groups': [{'id': 'OG000', 'title': 'Dyadic CARE (Supporters)', 'description': 'Supporters randomized to receive dyadic CARE (both dyad members attended both sessions and completed a workbook together)'}, {'id': 'OG001', 'title': 'Supporter-Only CARE (Supporters)', 'description': 'Supporters randomized to receive supporter-only CARE (only the supporter attended both sessions; the dyad completed a workbook together)'}, {'id': 'OG002', 'title': 'Waitlist Control (Supporters)', 'description': "Supporters randomized to receive waitlist CARE (invited to complete the CARE version of the survivor's choice following the completion of study measures)"}], 'classes': [{'categories': [{'measurements': [{'value': '4.61', 'spread': '2.93', 'groupId': 'OG000'}, {'value': '4.84', 'spread': '3.55', 'groupId': 'OG001'}, {'value': '0.33', 'spread': '2.54', 'groupId': 'OG002'}]}]}], 'paramType': 'MEAN', 'timeFrame': 'Baseline, 1 month', 'description': 'Sum score on a knowledge questionnaire reflecting CARE concepts, completed by the supporter. Range: 9 to 45; higher scores indicate more knowledge about CARE concepts.', 'unitOfMeasure': 'Points', 'dispersionType': 'Standard Deviation', 'reportingStatus': 'POSTED', 'populationDescription': 'Because this is a change score, participants were excluded listwise if they had missing data at one or both assessments.'}, {'type': 'PRIMARY', 'title': 'Change in Survivor Confusion About Help-seeking Behavior at 1 Month Post-baseline (Self Report)', 'denoms': [{'units': 'Participants', 'counts': [{'value': '19', 'groupId': 'OG000'}, {'value': '21', 'groupId': 'OG001'}, {'value': '21', 'groupId': 'OG002'}]}], 'groups': [{'id': 'OG000', 'title': 'Dyadic CARE (Survivors)', 'description': 'Survivors randomized to receive dyadic CARE (both dyad members attended both sessions and completed a workbook together)'}, {'id': 'OG001', 'title': 'Supporter-Only CARE (Survivors)', 'description': 'Survivors randomized to receive supporter-only CARE (only the supporter attended both sessions; the dyad completed a workbook together)'}, {'id': 'OG002', 'title': 'Waitlist Control (Survivors)', 'description': 'Survivors randomized to receive waitlist CARE (invited to complete the CARE version of their choice following the completion of study measures)'}], 'classes': [{'categories': [{'measurements': [{'value': '-2.21', 'spread': '4.04', 'groupId': 'OG000'}, {'value': '-1.14', 'spread': '3.64', 'groupId': 'OG001'}, {'value': '0.86', 'spread': '4.50', 'groupId': 'OG002'}]}]}], 'paramType': 'MEAN', 'timeFrame': 'Baseline, 1 month', 'description': 'Sum score on 4-item measure created for this study, completed by survivor. Range: 4 to 20; higher scores indicate greater confusion.', 'unitOfMeasure': 'score on a scale', 'dispersionType': 'Standard Deviation', 'reportingStatus': 'POSTED', 'populationDescription': 'Because this is a change score, participants were excluded listwise if they had missing data at one or both assessments.'}, {'type': 'PRIMARY', 'title': 'Change in Supporter Confusion About Helping Behavior at 1 Month Post-baseline (Self Report)', 'denoms': [{'units': 'Participants', 'counts': [{'value': '20', 'groupId': 'OG000'}, {'value': '20', 'groupId': 'OG001'}, {'value': '20', 'groupId': 'OG002'}]}], 'groups': [{'id': 'OG000', 'title': 'Dyadic CARE (Supporters)', 'description': 'Supporters randomized to receive dyadic CARE (both dyad members attended both sessions and completed a workbook together)'}, {'id': 'OG001', 'title': 'Supporter-Only CARE (Supporters)', 'description': 'Supporters randomized to receive supporter-only CARE (only the supporter attended both sessions; the dyad completed a workbook together)'}, {'id': 'OG002', 'title': 'Waitlist Control (Supporters)', 'description': "Supporters randomized to receive waitlist CARE (invited to complete the CARE version of the survivor's choice following the completion of study measures)"}], 'classes': [{'categories': [{'measurements': [{'value': '-4.35', 'spread': '3.88', 'groupId': 'OG000'}, {'value': '-3.70', 'spread': '3.42', 'groupId': 'OG001'}, {'value': '-1.85', 'spread': '3.23', 'groupId': 'OG002'}]}]}], 'paramType': 'MEAN', 'timeFrame': 'Baseline, 1 month', 'description': 'Sum score on the Confusion subscale of the Impact on Friends scale, completed by supporter. Range: 6 to 30; higher scores indicate greater confusion about helping behavior.', 'unitOfMeasure': 'score on a scale', 'dispersionType': 'Standard Deviation', 'reportingStatus': 'POSTED', 'populationDescription': 'Because this is a change score, participants were excluded listwise if they had missing data at one or both assessments.'}, {'type': 'PRIMARY', 'title': 'Survivor Disclosure Frequency to Supporter at 1 Month Post-baseline (Self Report)', 'denoms': [{'units': 'Participants', 'counts': [{'value': '21', 'groupId': 'OG000'}, {'value': '21', 'groupId': 'OG001'}, {'value': '21', 'groupId': 'OG002'}]}], 'groups': [{'id': 'OG000', 'title': 'Dyadic CARE (Survivors)', 'description': 'Survivors randomized to receive dyadic CARE (both dyad members attended both sessions and completed a workbook together)'}, {'id': 'OG001', 'title': 'Supporter-Only CARE (Survivors)', 'description': 'Survivors randomized to receive supporter-only CARE (only the supporter attended both sessions; the dyad completed a workbook together)'}, {'id': 'OG002', 'title': 'Waitlist Control (Survivors)', 'description': 'Survivors randomized to receive waitlist CARE (invited to complete the CARE version of their choice following the completion of study measures)'}], 'classes': [{'categories': [{'measurements': [{'value': '2.67', 'spread': '0.21', 'groupId': 'OG000'}, {'value': '3.02', 'spread': '0.21', 'groupId': 'OG001'}, {'value': '2.66', 'spread': '0.21', 'groupId': 'OG002'}]}]}], 'paramType': 'MEAN', 'timeFrame': '1 month', 'description': 'Single item representing frequency of disclosures to supporter in past month, completed by survivor, adapted from the Early Intervention Clinic Disclosure scale. Survivor will input a numerical response representing number of disclosures. Higher scores indicate more frequent disclosure.', 'unitOfMeasure': 'number of disclosures', 'dispersionType': 'Standard Error', 'reportingStatus': 'POSTED', 'populationDescription': 'Participants were excluded if they did not complete this scale.'}, {'type': 'PRIMARY', 'title': 'Supporter Overt Hostile Reactions to Disclosure at 1 Month Post-baseline (Informant Report)', 'denoms': [{'units': 'Participants', 'counts': [{'value': '15', 'groupId': 'OG000'}, {'value': '18', 'groupId': 'OG001'}, {'value': '17', 'groupId': 'OG002'}]}], 'groups': [{'id': 'OG000', 'title': 'Dyadic CARE (Survivors)', 'description': 'Survivors randomized to receive dyadic CARE (both dyad members attended both sessions and completed a workbook together)'}, {'id': 'OG001', 'title': 'Supporter-Only CARE (Survivors)', 'description': 'Survivors randomized to receive supporter-only CARE (only the supporter attended both sessions; the dyad completed a workbook together)'}, {'id': 'OG002', 'title': 'Waitlist Control (Survivors)', 'description': 'Survivors randomized to receive waitlist CARE (invited to complete the CARE version of their choice following the completion of study measures)'}], 'classes': [{'categories': [{'measurements': [{'value': '1.41', 'spread': '0.53', 'groupId': 'OG000'}, {'value': '2.96', 'spread': '0.49', 'groupId': 'OG001'}, {'value': '2.49', 'spread': '0.50', 'groupId': 'OG002'}]}]}], 'paramType': 'MEAN', 'timeFrame': '1 month', 'description': "Sum score on Turning Against subscale of the Social Reactions Questionnaire - Shortened, completed by survivor in reference to supporter's reactions in past month. Range: 0 to 24; higher scores indicate more frequent hostile negative reactions.", 'unitOfMeasure': 'score on a scale', 'dispersionType': 'Standard Error', 'reportingStatus': 'POSTED', 'populationDescription': 'Only assessed among survivors reporting past-month disclosure to the supporter'}, {'type': 'PRIMARY', 'title': 'Supporter Subtly Unsupportive Reactions to Disclosure at 1 Month Post-baseline (Informant Report)', 'denoms': [{'units': 'Participants', 'counts': [{'value': '15', 'groupId': 'OG000'}, {'value': '18', 'groupId': 'OG001'}, {'value': '17', 'groupId': 'OG002'}]}], 'groups': [{'id': 'OG000', 'title': 'Dyadic CARE (Survivors)', 'description': 'Survivors randomized to receive dyadic CARE (both dyad members attended both sessions and completed a workbook together)'}, {'id': 'OG001', 'title': 'Supporter-Only CARE (Survivors)', 'description': 'Survivors randomized to receive supporter-only CARE (only the supporter attended both sessions; the dyad completed a workbook together)'}, {'id': 'OG002', 'title': 'Waitlist Control (Survivors)', 'description': 'Survivors randomized to receive waitlist CARE (invited to complete the CARE version of their choice following the completion of study measures)'}], 'classes': [{'categories': [{'measurements': [{'value': '2.04', 'spread': '0.57', 'groupId': 'OG000'}, {'value': '2.23', 'spread': '0.52', 'groupId': 'OG001'}, {'value': '3.34', 'spread': '0.54', 'groupId': 'OG002'}]}]}], 'paramType': 'MEAN', 'timeFrame': '1 month', 'description': "Sum score on Unsupportive Acknowledgment subscale of the Social Reactions Questionnaire - Shortened, completed by survivor in reference to supporter's reactions in past month. Range: 0 to 24; higher scores indicate more frequent subtly unsupportive reactions.", 'unitOfMeasure': 'score on a scale', 'dispersionType': 'Standard Error', 'reportingStatus': 'POSTED', 'populationDescription': 'Only assessed among survivors reporting past-month disclosure to the supporter'}, {'type': 'PRIMARY', 'title': 'Change in Supporter Responsiveness at 1 Month Post-baseline (Informant Report)', 'denoms': [{'units': 'Participants', 'counts': [{'value': '19', 'groupId': 'OG000'}, {'value': '21', 'groupId': 'OG001'}, {'value': '21', 'groupId': 'OG002'}]}], 'groups': [{'id': 'OG000', 'title': 'Dyadic CARE (Survivors)', 'description': 'Survivors randomized to receive dyadic CARE (both dyad members attended both sessions and completed a workbook together)'}, {'id': 'OG001', 'title': 'Supporter-Only CARE (Survivors)', 'description': 'Survivors randomized to receive supporter-only CARE (only the supporter attended both sessions; the dyad completed a workbook together)'}, {'id': 'OG002', 'title': 'Waitlist Control (Survivors)', 'description': 'Survivors randomized to receive waitlist CARE (invited to complete the CARE version of their choice following the completion of study measures)'}], 'classes': [{'categories': [{'measurements': [{'value': '-2.21', 'spread': '5.90', 'groupId': 'OG000'}, {'value': '-0.10', 'spread': '7.49', 'groupId': 'OG001'}, {'value': '0.14', 'spread': '8.24', 'groupId': 'OG002'}]}]}], 'paramType': 'MEAN', 'timeFrame': 'Baseline & 1 month', 'description': 'Sum score on the Responsiveness subscale of the Perceived Responsiveness and Insensitivity scale, completed by survivor in reference to past month. Range: 0 to 40; higher scores indicate greater responsiveness.', 'unitOfMeasure': 'score on a scale', 'dispersionType': 'Standard Deviation', 'reportingStatus': 'POSTED', 'populationDescription': 'Because this is a change score, participants were excluded listwise if they had missing data at one or both assessments.'}, {'type': 'PRIMARY', 'title': 'Change in Survivor PTSD Symptom Severity at 3 Months Post-baseline (Self Report)', 'denoms': [{'units': 'Participants', 'counts': [{'value': '17', 'groupId': 'OG000'}, {'value': '19', 'groupId': 'OG001'}, {'value': '21', 'groupId': 'OG002'}]}], 'groups': [{'id': 'OG000', 'title': 'Dyadic CARE (Survivors)', 'description': 'Survivors randomized to receive dyadic CARE (both dyad members attended both sessions and completed a workbook together)'}, {'id': 'OG001', 'title': 'Supporter-Only CARE (Survivors)', 'description': 'Survivors randomized to receive supporter-only CARE (only the supporter attended both sessions; the dyad completed a workbook together)'}, {'id': 'OG002', 'title': 'Waitlist Control (Survivors)', 'description': 'Survivors randomized to receive waitlist CARE (invited to complete the CARE version of their choice following the completion of study measures)'}], 'classes': [{'categories': [{'measurements': [{'value': '-12.12', 'spread': '17.54', 'groupId': 'OG000'}, {'value': '-16.58', 'spread': '13.32', 'groupId': 'OG001'}, {'value': '-16.25', 'spread': '13.32', 'groupId': 'OG002'}]}]}], 'paramType': 'MEAN', 'timeFrame': 'Baseline, 3 months', 'description': 'Sum score on PTSD Checklist-5 (PCL-5), completed by survivor in reference to past month. Range: 0-80; higher scores indicate greater severity of PTSD symptoms.', 'unitOfMeasure': 'score on a scale', 'dispersionType': 'Standard Deviation', 'reportingStatus': 'POSTED', 'populationDescription': 'Because this is a change score, participants were excluded listwise if they had missing data at one or both assessments.'}, {'type': 'PRIMARY', 'title': 'Survivor Provisional PTSD Diagnostic Status at 3 Months Post-baseline (Self Report)', 'denoms': [{'units': 'Participants', 'counts': [{'value': '17', 'groupId': 'OG000'}, {'value': '19', 'groupId': 'OG001'}, {'value': '21', 'groupId': 'OG002'}]}], 'groups': [{'id': 'OG000', 'title': 'Dyadic CARE (Survivors)', 'description': 'Survivors randomized to receive dyadic CARE (both dyad members attended both sessions and completed a workbook together)'}, {'id': 'OG001', 'title': 'Supporter-Only CARE (Survivors)', 'description': 'Survivors randomized to receive supporter-only CARE (only the supporter attended both sessions; the dyad completed a workbook together)'}, {'id': 'OG002', 'title': 'Waitlist Control (Survivors)', 'description': 'Survivors randomized to receive waitlist CARE (invited to complete the CARE version of their choice following the completion of study measures)'}], 'classes': [{'categories': [{'measurements': [{'value': '8', 'groupId': 'OG000'}, {'value': '5', 'groupId': 'OG001'}, {'value': '9', 'groupId': 'OG002'}]}]}], 'paramType': 'COUNT_OF_PARTICIPANTS', 'timeFrame': '3 months', 'description': 'Provisional PTSD diagnostic status based on PTSD Checklist-5 (PCL-5), completed by survivor in reference to past month. Survivors will be considered to have a provisional diagnosis if the following items are rated as 2 = "Moderately" or higher: one Criterion B item (questions 1-5), one Criterion C item (questions 6-7), two Criterion D items (questions 8-14), and two Criterion E items (questions 15-20).', 'unitOfMeasure': 'Participants', 'reportingStatus': 'POSTED', 'populationDescription': 'Participants were excluded if they did not complete the scale at 3 months post baseline'}, {'type': 'PRIMARY', 'title': 'Change in Survivor Stress at 3 Months Post-baseline (Self Report)', 'denoms': [{'units': 'Participants', 'counts': [{'value': '19', 'groupId': 'OG000'}, {'value': '20', 'groupId': 'OG001'}, {'value': '21', 'groupId': 'OG002'}]}], 'groups': [{'id': 'OG000', 'title': 'Dyadic CARE (Survivors)', 'description': 'Survivors randomized to receive dyadic CARE (both dyad members attended both sessions and completed a workbook together)'}, {'id': 'OG001', 'title': 'Supporter-Only CARE (Survivors)', 'description': 'Survivors randomized to receive supporter-only CARE (only the supporter attended both sessions; the dyad completed a workbook together)'}, {'id': 'OG002', 'title': 'Waitlist Control (Survivors)', 'description': 'Survivors randomized to receive waitlist CARE (invited to complete the CARE version of their choice following the completion of study measures)'}], 'classes': [{'categories': [{'measurements': [{'value': '-1.66', 'spread': '5.39', 'groupId': 'OG000'}, {'value': '-2.42', 'spread': '3.56', 'groupId': 'OG001'}, {'value': '-1.38', 'spread': '3.58', 'groupId': 'OG002'}]}]}], 'paramType': 'MEAN', 'timeFrame': 'Baseline, 3 months', 'description': 'Sum score on the Stress subscale of the Depression and Anxiety Stress Scales (DASS-21), completed by survivor in reference to past week. Range: 0 to 21; higher scores indicate greater stress.', 'unitOfMeasure': 'score on a scale', 'dispersionType': 'Standard Deviation', 'reportingStatus': 'POSTED', 'populationDescription': 'Because this is a change score, participants were excluded listwise if they had missing data at one or both assessments.'}, {'type': 'PRIMARY', 'title': 'Change in Supporter Stress at 3 Months Post-baseline (Self Report)', 'denoms': [{'units': 'Participants', 'counts': [{'value': '20', 'groupId': 'OG000'}, {'value': '18', 'groupId': 'OG001'}, {'value': '20', 'groupId': 'OG002'}]}], 'groups': [{'id': 'OG000', 'title': 'Dyadic CARE (Supporters)', 'description': 'Supporters randomized to receive dyadic CARE (both dyad members attended both sessions and completed a workbook together)'}, {'id': 'OG001', 'title': 'Supporter-Only CARE (Supporters)', 'description': 'Supporters randomized to receive supporter-only CARE (only the supporter attended both sessions; the dyad completed a workbook together)'}, {'id': 'OG002', 'title': 'Waitlist Control (Supporters)', 'description': "Supporters randomized to receive waitlist CARE (invited to complete the CARE version of the survivor's choice following the completion of study measures)"}], 'classes': [{'categories': [{'measurements': [{'value': '-2.15', 'spread': '3.30', 'groupId': 'OG000'}, {'value': '-1.22', 'spread': '3.32', 'groupId': 'OG001'}, {'value': '-0.65', 'spread': '3.07', 'groupId': 'OG002'}]}]}], 'paramType': 'MEAN', 'timeFrame': 'Baseline, 3 months', 'description': 'Sum score on the Stress subscale of the Depression and Anxiety Stress Scales (DASS-21), completed by supporter in reference to past week. Range: 0 to 21; higher scores indicate greater stress.', 'unitOfMeasure': 'score on a scale', 'dispersionType': 'Standard Deviation', 'reportingStatus': 'POSTED', 'populationDescription': 'Because this is a change score, participants were excluded listwise if they had missing data at one or both assessments.'}, {'type': 'PRIMARY', 'title': 'Change in Survivor Perceived Relationship Quality at 3 Months Post-baseline (Self Report)', 'denoms': [{'units': 'Participants', 'counts': [{'value': '19', 'groupId': 'OG000'}, {'value': '20', 'groupId': 'OG001'}, {'value': '21', 'groupId': 'OG002'}]}], 'groups': [{'id': 'OG000', 'title': 'Dyadic CARE (Survivors)', 'description': 'Survivors randomized to receive dyadic CARE (both dyad members attended both sessions and completed a workbook together)'}, {'id': 'OG001', 'title': 'Supporter-Only CARE (Survivors)', 'description': 'Survivors randomized to receive supporter-only CARE (only the supporter attended both sessions; the dyad completed a workbook together)'}, {'id': 'OG002', 'title': 'Waitlist Control (Survivors)', 'description': 'Survivors randomized to receive waitlist CARE (invited to complete the CARE version of their choice following the completion of study measures)'}], 'classes': [{'categories': [{'measurements': [{'value': '-0.39', 'spread': '2.50', 'groupId': 'OG000'}, {'value': '-1.60', 'spread': '4.45', 'groupId': 'OG001'}, {'value': '-1.76', 'spread': '4.12', 'groupId': 'OG002'}]}]}], 'paramType': 'MEAN', 'timeFrame': 'Baseline, 3 months', 'description': 'Sum score on the Relationship Assessment Scale, completed by survivor. Range: 7 to 35; higher scores indicate greater relationship quality.', 'unitOfMeasure': 'score on a scale', 'dispersionType': 'Standard Deviation', 'reportingStatus': 'POSTED', 'populationDescription': 'Because this is a change score, participants were excluded listwise if they had missing data at one or both assessments.'}, {'type': 'PRIMARY', 'title': 'Change in Supporter Perceived Relationship Quality at 3 Months Post-baseline (Self Report)', 'denoms': [{'units': 'Participants', 'counts': [{'value': '20', 'groupId': 'OG000'}, {'value': '18', 'groupId': 'OG001'}, {'value': '20', 'groupId': 'OG002'}]}], 'groups': [{'id': 'OG000', 'title': 'Dyadic CARE (Supporters)', 'description': 'Supporters randomized to receive dyadic CARE (both dyad members attended both sessions and completed a workbook together)'}, {'id': 'OG001', 'title': 'Supporter-Only CARE (Supporters)', 'description': 'Supporters randomized to receive supporter-only CARE (only the supporter attended both sessions; the dyad completed a workbook together)'}, {'id': 'OG002', 'title': 'Waitlist Control (Supporters)', 'description': "Supporters randomized to receive waitlist CARE (invited to complete the CARE version of the survivor's choice following the completion of study measures)"}], 'classes': [{'categories': [{'measurements': [{'value': '0.35', 'spread': '3.94', 'groupId': 'OG000'}, {'value': '0.39', 'spread': '2.00', 'groupId': 'OG001'}, {'value': '-2.10', 'spread': '4.33', 'groupId': 'OG002'}]}]}], 'paramType': 'MEAN', 'timeFrame': 'Baseline, 3 months', 'description': 'Sum score on the Relationship Assessment Scale, completed by supporter. 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Range: 0 to 10; higher scores indicate greater willingness.', 'unitOfMeasure': 'score on a scale', 'dispersionType': 'Standard Deviation', 'reportingStatus': 'POSTED', 'populationDescription': 'Participants were excluded if they did not complete this scale.'}, {'type': 'SECONDARY', 'title': 'Survivor Participation in Criminal Justice Process at 1 Month Post-baseline (Self Report)', 'denoms': [{'units': 'Participants', 'counts': [{'value': '21', 'groupId': 'OG000'}, {'value': '21', 'groupId': 'OG001'}, {'value': '21', 'groupId': 'OG002'}]}], 'groups': [{'id': 'OG000', 'title': 'Dyadic CARE (Survivors)', 'description': 'Survivors randomized to receive dyadic CARE (both dyad members attended both sessions and completed a workbook together)'}, {'id': 'OG001', 'title': 'Supporter-Only CARE (Survivors)', 'description': 'Survivors randomized to receive supporter-only CARE (only the supporter attended both sessions; the dyad completed a workbook together)'}, {'id': 'OG002', 'title': 'Waitlist Control (Survivors)', 'description': 'Survivors randomized to receive waitlist CARE (invited to complete the CARE version of their choice following the completion of study measures)'}], 'classes': [{'categories': [{'measurements': [{'value': '0.64', 'spread': '0.07', 'groupId': 'OG000'}, {'value': '0.49', 'spread': '0.07', 'groupId': 'OG001'}, {'value': '0.52', 'spread': '0.07', 'groupId': 'OG002'}]}]}], 'paramType': 'MEAN', 'timeFrame': '1 month', 'description': 'Mean score on measure created for this study, completed by survivor. Range: 0 to 1; higher scores indicate greater participation.', 'unitOfMeasure': 'score on a scale', 'dispersionType': 'Standard Error', 'reportingStatus': 'POSTED', 'populationDescription': 'Participants were excluded if they did not complete this scale.'}, {'type': 'SECONDARY', 'title': 'Change in Survivor Depression at 3 Months Post-baseline (Self Report)', 'denoms': [{'units': 'Participants', 'counts': [{'value': '19', 'groupId': 'OG000'}, {'value': '20', 'groupId': 'OG001'}, {'value': '21', 'groupId': 'OG002'}]}], 'groups': [{'id': 'OG000', 'title': 'Dyadic CARE (Survivors)', 'description': 'Survivors randomized to receive dyadic CARE (both dyad members attended both sessions and completed a workbook together)'}, {'id': 'OG001', 'title': 'Supporter-Only CARE (Survivors)', 'description': 'Survivors randomized to receive supporter-only CARE (only the supporter attended both sessions; the dyad completed a workbook together)'}, {'id': 'OG002', 'title': 'Waitlist Control (Survivors)', 'description': 'Survivors randomized to receive waitlist CARE (invited to complete the CARE version of their choice following the completion of study measures)'}], 'classes': [{'categories': [{'measurements': [{'value': '-1.58', 'spread': '6.15', 'groupId': 'OG000'}, {'value': '-3.00', 'spread': '3.15', 'groupId': 'OG001'}, {'value': '-2.52', 'spread': '4.57', 'groupId': 'OG002'}]}]}], 'paramType': 'MEAN', 'timeFrame': 'Baseline, 3 months', 'description': 'Sum score on the Depression subscale of the Depression and Anxiety Stress Scales (DASS-21), completed by survivor in reference to past week. 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Range: 0 to 120; higher scores indicate more flourishing.', 'unitOfMeasure': 'score on a scale', 'dispersionType': 'Standard Deviation', 'reportingStatus': 'POSTED', 'populationDescription': 'Because this is a change score, participants were excluded listwise if they had missing data at one or both assessments.'}, {'type': 'SECONDARY', 'title': 'Change in Supporter Flourishing at 3 Months Post-baseline (Self Report)', 'denoms': [{'units': 'Participants', 'counts': [{'value': '20', 'groupId': 'OG000'}, {'value': '20', 'groupId': 'OG001'}, {'value': '20', 'groupId': 'OG002'}]}], 'groups': [{'id': 'OG000', 'title': 'Dyadic CARE (Supporters)', 'description': 'Supporters randomized to receive dyadic CARE (both dyad members attended both sessions and completed a workbook together)'}, {'id': 'OG001', 'title': 'Supporter-Only CARE (Supporters)', 'description': 'Supporters randomized to receive supporter-only CARE (only the supporter attended both sessions; the dyad completed a workbook together)'}, {'id': 'OG002', 'title': 'Waitlist Control (Supporters)', 'description': "Supporters randomized to receive waitlist CARE (invited to complete the CARE version of the survivor's choice following the completion of study measures)"}], 'classes': [{'categories': [{'measurements': [{'value': '1.65', 'spread': '10.39', 'groupId': 'OG000'}, {'value': '5.22', 'spread': '9.52', 'groupId': 'OG001'}, {'value': '-7.33', 'spread': '17.39', 'groupId': 'OG002'}]}]}], 'paramType': 'MEAN', 'timeFrame': 'Baseline, 3 months', 'description': 'Sum score on Flourishing Index Measure, completed by supporter. 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Range: 0 to 16; higher scores indicate more frequent positive reactions.", 'unitOfMeasure': 'score on a scale', 'dispersionType': 'Standard Error', 'reportingStatus': 'POSTED', 'populationDescription': 'Only assessed among survivors reporting past-month disclosure to the supporter'}, {'type': 'SECONDARY', 'title': 'Change in Survivor Typical Alcohol Consumption (Quantity) at 3 Months Post-baseline (Self Report)', 'denoms': [{'units': 'Participants', 'counts': [{'value': '19', 'groupId': 'OG000'}, {'value': '20', 'groupId': 'OG001'}, {'value': '20', 'groupId': 'OG002'}]}], 'groups': [{'id': 'OG000', 'title': 'Dyadic CARE (Survivors)', 'description': 'Survivors randomized to receive dyadic CARE (both dyad members attended both sessions and completed a workbook together)'}, {'id': 'OG001', 'title': 'Supporter-Only CARE (Survivors)', 'description': 'Survivors randomized to receive supporter-only CARE (only the supporter attended both sessions; the dyad completed a workbook together)'}, {'id': 'OG002', 'title': 'Waitlist Control (Survivors)', 'description': 'Survivors randomized to receive waitlist CARE (invited to complete the CARE version of their choice following the completion of study measures)'}], 'classes': [{'categories': [{'measurements': [{'value': '0.58', 'spread': '5.96', 'groupId': 'OG000'}, {'value': '-1.80', 'spread': '2.89', 'groupId': 'OG001'}, {'value': '-0.25', 'spread': '9.30', 'groupId': 'OG002'}]}]}], 'paramType': 'MEAN', 'timeFrame': 'Baseline, 3 months', 'description': 'Number of typical drinks per week in past month reported by survivor on the Daily Drinking Questionnaire', 'unitOfMeasure': 'drinks per week', 'dispersionType': 'Standard Deviation', 'reportingStatus': 'POSTED', 'populationDescription': 'Because this is a change score, participants were excluded listwise if they had missing data at one or both assessments.'}, {'type': 'SECONDARY', 'title': 'Change in Survivor Typical Alcohol Consumption (Frequency) at 3 Months Post-baseline (Self Report)', 'denoms': [{'units': 'Participants', 'counts': [{'value': '19', 'groupId': 'OG000'}, {'value': '20', 'groupId': 'OG001'}, {'value': '20', 'groupId': 'OG002'}]}], 'groups': [{'id': 'OG000', 'title': 'Dyadic CARE (Survivors)', 'description': 'Survivors randomized to receive dyadic CARE (both dyad members attended both sessions and completed a workbook together)'}, {'id': 'OG001', 'title': 'Supporter-Only CARE (Survivors)', 'description': 'Survivors randomized to receive supporter-only CARE (only the supporter attended both sessions; the dyad completed a workbook together)'}, {'id': 'OG002', 'title': 'Waitlist Control (Survivors)', 'description': 'Survivors randomized to receive waitlist CARE (invited to complete the CARE version of their choice following the completion of study measures)'}], 'classes': [{'categories': [{'measurements': [{'value': '0.32', 'spread': '1.60', 'groupId': 'OG000'}, {'value': '-0.40', 'spread': '0.99', 'groupId': 'OG001'}, {'value': '0.25', 'spread': '1.65', 'groupId': 'OG002'}]}]}], 'paramType': 'MEAN', 'timeFrame': 'Baseline, 3 months', 'description': 'Number of typical drinking days per week in past month reported by survivor on the Daily Drinking Questionnaire. Range: 0 to 7.', 'unitOfMeasure': 'days per week', 'dispersionType': 'Standard Deviation', 'reportingStatus': 'POSTED', 'populationDescription': 'Because this is a change score, participants were excluded listwise if they had missing data at one or both assessments.'}, {'type': 'SECONDARY', 'title': 'Change in Survivor Typical Alcohol Consumption (Hours) at 3 Months Post-baseline (Self Report)', 'denoms': [{'units': 'Participants', 'counts': [{'value': '19', 'groupId': 'OG000'}, {'value': '19', 'groupId': 'OG001'}, {'value': '20', 'groupId': 'OG002'}]}], 'groups': [{'id': 'OG000', 'title': 'Dyadic CARE (Survivors)', 'description': 'Survivors randomized to receive dyadic CARE (both dyad members attended both sessions and completed a workbook together)'}, {'id': 'OG001', 'title': 'Supporter-Only CARE (Survivors)', 'description': 'Survivors randomized to receive supporter-only CARE (only the supporter attended both sessions; the dyad completed a workbook together)'}, {'id': 'OG002', 'title': 'Waitlist Control (Survivors)', 'description': 'Survivors randomized to receive waitlist CARE (invited to complete the CARE version of their choice following the completion of study measures)'}], 'classes': [{'categories': [{'measurements': [{'value': '1.32', 'spread': '7.45', 'groupId': 'OG000'}, {'value': '-0.79', 'spread': '3.87', 'groupId': 'OG001'}, {'value': '-1.95', 'spread': '8.51', 'groupId': 'OG002'}]}]}], 'paramType': 'MEAN', 'timeFrame': 'Baseline, 3 months', 'description': 'Number of typical drinking hours per week in past month reported by survivor on the Daily Drinking Questionnaire.', 'unitOfMeasure': 'hours per week', 'dispersionType': 'Standard Deviation', 'reportingStatus': 'POSTED', 'populationDescription': 'Because this is a change score, participants were excluded listwise if they had missing data at one or both assessments.'}, {'type': 'SECONDARY', 'title': 'Supporter Perceived Helping Ineffectiveness at 1 Month Post-baseline (Self Report)', 'denoms': [{'units': 'Participants', 'counts': [{'value': '21', 'groupId': 'OG000'}, {'value': '21', 'groupId': 'OG001'}, {'value': '21', 'groupId': 'OG002'}]}], 'groups': [{'id': 'OG000', 'title': 'Dyadic CARE (Supporters)', 'description': 'Supporters randomized to receive dyadic CARE (both dyad members attended both sessions and completed a workbook together)'}, {'id': 'OG001', 'title': 'Supporter-Only CARE (Supporters)', 'description': 'Supporters randomized to receive supporter-only CARE (only the supporter attended both sessions; the dyad completed a workbook together)'}, {'id': 'OG002', 'title': 'Waitlist Control (Supporters)', 'description': "Supporters randomized to receive waitlist CARE (invited to complete the CARE version of the survivor's choice following the completion of study measures)"}], 'classes': [{'categories': [{'measurements': [{'value': '12.13', 'spread': '0.91', 'groupId': 'OG000'}, {'value': '12.78', 'spread': '0.90', 'groupId': 'OG001'}, {'value': '14.57', 'spread': '0.91', 'groupId': 'OG002'}]}]}], 'paramType': 'MEAN', 'timeFrame': '1 month', 'description': 'Sum score on the Confusion subscale of the Impact on Friends measure, completed by supporter in reference to the past month. Range: 6 to 30; higher scores indicate greater perceived ineffectiveness.', 'unitOfMeasure': 'score on a scale', 'dispersionType': 'Standard Error', 'reportingStatus': 'POSTED', 'populationDescription': 'Participants were excluded if they did not complete this scale.'}, {'type': 'SECONDARY', 'title': 'Supporter Distress in Helping at 1 Month Post-baseline (Self Report)', 'denoms': [{'units': 'Participants', 'counts': [{'value': '21', 'groupId': 'OG000'}, {'value': '21', 'groupId': 'OG001'}, {'value': '21', 'groupId': 'OG002'}]}], 'groups': [{'id': 'OG000', 'title': 'Dyadic CARE (Supporters)', 'description': 'Supporters randomized to receive dyadic CARE (both dyad members attended both sessions and completed a workbook together)'}, {'id': 'OG001', 'title': 'Supporter-Only CARE (Supporters)', 'description': 'Supporters randomized to receive supporter-only CARE (only the supporter attended both sessions; the dyad completed a workbook together)'}, {'id': 'OG002', 'title': 'Waitlist Control (Supporters)', 'description': "Supporters randomized to receive waitlist CARE (invited to complete the CARE version of the survivor's choice following the completion of study measures)"}], 'classes': [{'categories': [{'measurements': [{'value': '53.59', 'spread': '2.82', 'groupId': 'OG000'}, {'value': '55.99', 'spread': '2.80', 'groupId': 'OG001'}, {'value': '61.57', 'spread': '2.83', 'groupId': 'OG002'}]}]}], 'paramType': 'MEAN', 'timeFrame': '1 month', 'description': 'Sum score on the Emotional Distress subscale of the Impact on Friends measure, completed by supporter in reference to the past month. Range: 24 to 120; higher scores indicate greater distress.', 'unitOfMeasure': 'score on a scale', 'dispersionType': 'Standard Error', 'reportingStatus': 'POSTED', 'populationDescription': 'Participants were excluded if they did not complete this scale.'}, {'type': 'SECONDARY', 'title': 'Supporter Accommodation of Survivor PTSD Symptoms at 1 Month Post-baseline (Self Report)', 'denoms': [{'units': 'Participants', 'counts': [{'value': '20', 'groupId': 'OG000'}, {'value': '20', 'groupId': 'OG001'}, {'value': '20', 'groupId': 'OG002'}]}], 'groups': [{'id': 'OG000', 'title': 'Dyadic CARE (Supporters)', 'description': 'Supporters randomized to receive dyadic CARE (both dyad members attended both sessions and completed a workbook together)'}, {'id': 'OG001', 'title': 'Supporter-Only CARE (Supporters)', 'description': 'Supporters randomized to receive supporter-only CARE (only the supporter attended both sessions; the dyad completed a workbook together)'}, {'id': 'OG002', 'title': 'Waitlist Control (Supporters)', 'description': "Supporters randomized to receive waitlist CARE (invited to complete the CARE version of the survivor's choice following the completion of study measures)"}], 'classes': [{'categories': [{'measurements': [{'value': '12.78', 'spread': '2.96', 'groupId': 'OG000'}, {'value': '8.64', 'spread': '2.95', 'groupId': 'OG001'}, {'value': '17.66', 'spread': '2.01', 'groupId': 'OG002'}]}]}], 'paramType': 'MEAN', 'timeFrame': '1 month', 'description': "Sum score on the Significant Others' Responses to Trauma Scale (SORTS), completed by supporter in reference to the past month. Range: 0 to 112; higher scores indicate greater accommodation.", 'unitOfMeasure': 'score on a scale', 'dispersionType': 'Standard Error', 'reportingStatus': 'POSTED', 'populationDescription': 'Participants were excluded if they did not complete this scale.'}, {'type': 'SECONDARY', 'title': 'Change in Survivor Cannabis Use Frequency at 3 Months Post-baseline (Self Report)', 'denoms': [{'units': 'Participants', 'counts': [{'value': '19', 'groupId': 'OG000'}, {'value': '19', 'groupId': 'OG001'}, {'value': '21', 'groupId': 'OG002'}]}], 'groups': [{'id': 'OG000', 'title': 'Dyadic CARE (Survivors)', 'description': 'Survivors randomized to receive dyadic CARE (both dyad members attended both sessions and completed a workbook together)'}, {'id': 'OG001', 'title': 'Supporter-Only CARE (Survivors)', 'description': 'Survivors randomized to receive supporter-only CARE (only the supporter attended both sessions; the dyad completed a workbook together)'}, {'id': 'OG002', 'title': 'Waitlist Control (Survivors)', 'description': 'Survivors randomized to receive waitlist CARE (invited to complete the CARE version of their choice following the completion of study measures)'}], 'classes': [{'categories': [{'measurements': [{'value': '-0.11', 'spread': '1.79', 'groupId': 'OG000'}, {'value': '0.63', 'spread': '2.39', 'groupId': 'OG001'}, {'value': '-1.62', 'spread': '2.91', 'groupId': 'OG002'}]}]}], 'paramType': 'MEAN', 'timeFrame': 'Baseline, 3 months', 'description': 'Number of days of cannabis use in past 2 weeks, as reported by survivor. Range: 0 to 14.', 'unitOfMeasure': 'Days', 'dispersionType': 'Standard Deviation', 'reportingStatus': 'POSTED', 'populationDescription': 'Because this is a change score, participants were excluded listwise if they had missing data at one or both assessments.'}, {'type': 'SECONDARY', 'title': 'Change in Survivor Prescription Opioid Misuse Frequency at 3 Months Post-baseline (Self Report)', 'denoms': [{'units': 'Participants', 'counts': [{'value': '0', 'groupId': 'OG000'}, {'value': '0', 'groupId': 'OG001'}, {'value': '0', 'groupId': 'OG002'}]}], 'groups': [{'id': 'OG000', 'title': 'Dyadic CARE (Survivors)', 'description': 'Survivors randomized to receive dyadic CARE (both dyad members attended both sessions and completed a workbook together)'}, {'id': 'OG001', 'title': 'Supporter-Only CARE (Survivors)', 'description': 'Survivors randomized to receive supporter-only CARE (only the supporter attended both sessions; the dyad completed a workbook together)'}, {'id': 'OG002', 'title': 'Waitlist Control (Survivors)', 'description': 'Survivors randomized to receive waitlist CARE (invited to complete the CARE version of their choice following the completion of study measures)'}], 'timeFrame': 'Baseline, 3 months', 'description': 'Number of days of prescription opioid use not as prescribed in past 2 weeks, as reported by survivor. Range: 0 to 14.', 'reportingStatus': 'POSTED', 'populationDescription': 'Analyses could not be performed because no participants reported opioid use.'}, {'type': 'SECONDARY', 'title': 'Change in Survivor Non-prescription Opioid Use Frequency at 3 Months Post-baseline (Self Report)', 'denoms': [{'units': 'Participants', 'counts': [{'value': '0', 'groupId': 'OG000'}, {'value': '0', 'groupId': 'OG001'}, {'value': '0', 'groupId': 'OG002'}]}], 'groups': [{'id': 'OG000', 'title': 'Dyadic CARE (Survivors)', 'description': 'Survivors randomized to receive dyadic CARE (both dyad members attended both sessions and completed a workbook together)'}, {'id': 'OG001', 'title': 'Supporter-Only CARE (Survivors)', 'description': 'Survivors randomized to receive supporter-only CARE (only the supporter attended both sessions; the dyad completed a workbook together)'}, {'id': 'OG002', 'title': 'Waitlist Control (Survivors)', 'description': 'Survivors randomized to receive waitlist CARE (invited to complete the CARE version of their choice following the completion of study measures)'}], 'timeFrame': 'Baseline, 3 months', 'description': 'Number of days of non-prescription opioid use in past 2 weeks, as reported by survivor. Range: 0 to 14.', 'reportingStatus': 'POSTED', 'populationDescription': 'Analyses could not be performed because no participants reported non-prescription opioid use.'}, {'type': 'SECONDARY', 'title': 'Change in Survivor Prescription Amphetamine Misuse Frequency at 3 Months Post-baseline (Self Report)', 'denoms': [{'units': 'Participants', 'counts': [{'value': '19', 'groupId': 'OG000'}, {'value': '19', 'groupId': 'OG001'}, {'value': '21', 'groupId': 'OG002'}]}], 'groups': [{'id': 'OG000', 'title': 'Dyadic CARE (Survivors)', 'description': 'Survivors randomized to receive dyadic CARE (both dyad members attended both sessions and completed a workbook together)'}, {'id': 'OG001', 'title': 'Supporter-Only CARE (Survivors)', 'description': 'Survivors randomized to receive supporter-only CARE (only the supporter attended both sessions; the dyad completed a workbook together)'}, {'id': 'OG002', 'title': 'Waitlist Control (Survivors)', 'description': 'Survivors randomized to receive waitlist CARE (invited to complete the CARE version of their choice following the completion of study measures)'}], 'classes': [{'categories': [{'measurements': [{'value': '0.11', 'spread': '0.46', 'groupId': 'OG000'}, {'value': '-0.05', 'spread': '0.23', 'groupId': 'OG001'}, {'value': '0.24', 'spread': '1.09', 'groupId': 'OG002'}]}]}], 'paramType': 'MEAN', 'timeFrame': 'Baseline, 3 months', 'description': 'Number of days of prescription amphetamine use not as prescribed in past 2 weeks, as reported by survivor. Range: 0 to 14.', 'unitOfMeasure': 'Days', 'dispersionType': 'Standard Deviation', 'reportingStatus': 'POSTED', 'populationDescription': 'Because this is a change score, participants were excluded listwise if they had missing data at one or both assessments.'}, {'type': 'SECONDARY', 'title': 'Change in Survivor Methamphetamine Use Frequency at 3 Months Post-baseline (Self Report)', 'denoms': [{'units': 'Participants', 'counts': [{'value': '19', 'groupId': 'OG000'}, {'value': '21', 'groupId': 'OG001'}, {'value': '21', 'groupId': 'OG002'}]}], 'groups': [{'id': 'OG000', 'title': 'Dyadic CARE (Survivors)', 'description': 'Survivors randomized to receive dyadic CARE (both dyad members attended both sessions and completed a workbook together)'}, {'id': 'OG001', 'title': 'Supporter-Only CARE (Survivors)', 'description': 'Survivors randomized to receive supporter-only CARE (only the supporter attended both sessions; the dyad completed a workbook together)'}, {'id': 'OG002', 'title': 'Waitlist Control (Survivors)', 'description': 'Survivors randomized to receive waitlist CARE (invited to complete the CARE version of their choice following the completion of study measures)'}], 'classes': [{'categories': [{'measurements': [{'value': '0.16', 'spread': '0.69', 'groupId': 'OG000'}, {'value': '0.29', 'spread': '1.31', 'groupId': 'OG001'}, {'value': '-0.19', 'spread': '0.87', 'groupId': 'OG002'}]}]}], 'paramType': 'MEAN', 'timeFrame': 'Baseline, 3 months', 'description': 'Number of days of methamphetamine use in past 2 weeks, as reported by survivor. Range: 0 to 14.', 'unitOfMeasure': 'Days', 'dispersionType': 'Standard Deviation', 'reportingStatus': 'POSTED', 'populationDescription': 'Because this is a change score, participants were excluded listwise if they had missing data at one or both assessments.'}, {'type': 'SECONDARY', 'title': 'Change in Survivor Cigarette Use Frequency at 3 Months Post-baseline (Self Report)', 'denoms': [{'units': 'Participants', 'counts': [{'value': '19', 'groupId': 'OG000'}, {'value': '19', 'groupId': 'OG001'}, {'value': '21', 'groupId': 'OG002'}]}], 'groups': [{'id': 'OG000', 'title': 'Dyadic CARE (Survivors)', 'description': 'Survivors randomized to receive dyadic CARE (both dyad members attended both sessions and completed a workbook together)'}, {'id': 'OG001', 'title': 'Supporter-Only CARE (Survivors)', 'description': 'Survivors randomized to receive supporter-only CARE (only the supporter attended both sessions; the dyad completed a workbook together)'}, {'id': 'OG002', 'title': 'Waitlist Control (Survivors)', 'description': 'Survivors randomized to receive waitlist CARE (invited to complete the CARE version of their choice following the completion of study measures)'}], 'classes': [{'categories': [{'measurements': [{'value': '-0.05', 'spread': '0.23', 'groupId': 'OG000'}, {'value': '-0.16', 'spread': '0.37', 'groupId': 'OG001'}, {'value': '-0.10', 'spread': '0.44', 'groupId': 'OG002'}]}]}], 'paramType': 'MEAN', 'timeFrame': 'Baseline, 3 months', 'description': 'Number of days of cigarette use in past 2 weeks, as reported by survivor. Range: 0 to 14.', 'unitOfMeasure': 'Days', 'dispersionType': 'Standard Deviation', 'reportingStatus': 'POSTED', 'populationDescription': 'Because this is a change score, participants were excluded listwise if they had missing data at one or both assessments.'}, {'type': 'SECONDARY', 'title': 'Change in Survivor Cigarette Use Quantity at 3 Months Post-baseline (Self Report)', 'denoms': [{'units': 'Participants', 'counts': [{'value': '19', 'groupId': 'OG000'}, {'value': '20', 'groupId': 'OG001'}, {'value': '21', 'groupId': 'OG002'}]}], 'groups': [{'id': 'OG000', 'title': 'Dyadic CARE (Survivors)', 'description': 'Survivors randomized to receive dyadic CARE (both dyad members attended both sessions and completed a workbook together)'}, {'id': 'OG001', 'title': 'Supporter-Only CARE (Survivors)', 'description': 'Survivors randomized to receive supporter-only CARE (only the supporter attended both sessions; the dyad completed a workbook together)'}, {'id': 'OG002', 'title': 'Waitlist Control (Survivors)', 'description': 'Survivors randomized to receive waitlist CARE (invited to complete the CARE version of their choice following the completion of study measures)'}], 'classes': [{'categories': [{'measurements': [{'value': '-0.01', 'spread': '0.05', 'groupId': 'OG000'}, {'value': '-1.05', 'spread': '3.36', 'groupId': 'OG001'}, {'value': '-0.62', 'spread': '2.62', 'groupId': 'OG002'}]}]}], 'paramType': 'MEAN', 'timeFrame': 'Baseline, 3 months', 'description': 'Number of cigarettes smoked in a typical day in past 2 weeks, as reported by survivor.', 'unitOfMeasure': 'Cigarettes Per Day', 'dispersionType': 'Standard Deviation', 'reportingStatus': 'POSTED', 'populationDescription': 'Because this is a change score, participants were excluded listwise if they had missing data at one or both assessments.'}, {'type': 'OTHER_PRE_SPECIFIED', 'title': 'Survivor Disclosure Frequency to Supporter at 1 Month Post-baseline (Informant Report)', 'denoms': [{'units': 'Participants', 'counts': [{'value': '21', 'groupId': 'OG000'}, {'value': '21', 'groupId': 'OG001'}, {'value': '21', 'groupId': 'OG002'}]}], 'groups': [{'id': 'OG000', 'title': 'Dyadic CARE (Survivors)', 'description': 'Survivors randomized to receive dyadic CARE (both dyad members attended both sessions and completed a workbook together)'}, {'id': 'OG001', 'title': 'Supporter-Only CARE (Survivors)', 'description': 'Survivors randomized to receive supporter-only CARE (only the supporter attended both sessions; the dyad completed a workbook together)'}, {'id': 'OG002', 'title': 'Waitlist Control (Survivors)', 'description': 'Survivors randomized to receive waitlist CARE (invited to complete the CARE version of their choice following the completion of study measures)'}], 'classes': [{'categories': [{'measurements': [{'value': '2.56', 'spread': '0.21', 'groupId': 'OG000'}, {'value': '2.70', 'spread': '0.21', 'groupId': 'OG001'}, {'value': '2.02', 'spread': '0.20', 'groupId': 'OG002'}]}]}], 'paramType': 'MEAN', 'timeFrame': '1 month', 'description': "Single item representing frequency of survivor's disclosures to supporter in past month, completed by supporter, adapted from the Early Intervention Clinic Disclosure Scale. Participants were instructed to enter a numerical value corresponding to number of disclosures. Higher scores indicate more frequent disclosure.", 'unitOfMeasure': 'disclosures', 'dispersionType': 'Standard Error', 'reportingStatus': 'POSTED', 'populationDescription': 'Participants were excluded if they did not complete this item.'}, {'type': 'OTHER_PRE_SPECIFIED', 'title': 'Supporter Negative Reactions to Disclosure at 1 Month Post-baseline (Self Report)', 'denoms': [{'units': 'Participants', 'counts': [{'value': '18', 'groupId': 'OG000'}, {'value': '19', 'groupId': 'OG001'}, {'value': '11', 'groupId': 'OG002'}]}], 'groups': [{'id': 'OG000', 'title': 'Dyadic CARE (Supporters)', 'description': 'Supporters randomized to receive dyadic CARE (both dyad members attended both sessions and completed a workbook together)'}, {'id': 'OG001', 'title': 'Supporter-Only CARE (Supporters)', 'description': 'Supporters randomized to receive supporter-only CARE (only the supporter attended both sessions; the dyad completed a workbook together)'}, {'id': 'OG002', 'title': 'Waitlist Control (Supporters)', 'description': "Supporters randomized to receive waitlist CARE (invited to complete the CARE version of the survivor's choice following the completion of study measures)"}], 'classes': [{'categories': [{'measurements': [{'value': '2.22', 'spread': '3.12', 'groupId': 'OG000'}, {'value': '1.79', 'spread': '2.20', 'groupId': 'OG001'}, {'value': '4.19', 'spread': '3.62', 'groupId': 'OG002'}]}]}], 'paramType': 'MEAN', 'timeFrame': '1 month', 'description': "Sum score on Negative Reactions subscale of the Social Reactions Questionnaire - Shortened, completed by supporter in reference to supporter's reactions to survivor in past month. Range: 0 to 48; higher scores indicate more frequent negative reactions.", 'unitOfMeasure': 'score on a scale', 'dispersionType': 'Standard Deviation', 'reportingStatus': 'POSTED', 'populationDescription': 'Only assessed among supporters reporting past-month receipt of disclosure from the survivor'}, {'type': 'OTHER_PRE_SPECIFIED', 'title': 'Supporter Positive Reactions to Disclosure at 1 Month Post-baseline (Self Report)', 'denoms': [{'units': 'Participants', 'counts': [{'value': '18', 'groupId': 'OG000'}, {'value': '19', 'groupId': 'OG001'}, {'value': '11', 'groupId': 'OG002'}]}], 'groups': [{'id': 'OG000', 'title': 'Dyadic CARE (Supporters)', 'description': 'Supporters randomized to receive dyadic CARE (both dyad members attended both sessions and completed a workbook together)'}, {'id': 'OG001', 'title': 'Supporter-Only CARE (Supporters)', 'description': 'Supporters randomized to receive supporter-only CARE (only the supporter attended both sessions; the dyad completed a workbook together)'}, {'id': 'OG002', 'title': 'Waitlist Control (Supporters)', 'description': "Supporters randomized to receive waitlist CARE (invited to complete the CARE version of the survivor's choice following the completion of study measures)"}], 'classes': [{'categories': [{'measurements': [{'value': '8.56', 'spread': '0.63', 'groupId': 'OG000'}, {'value': '8.74', 'spread': '0.69', 'groupId': 'OG001'}, {'value': '9.36', 'spread': '0.99', 'groupId': 'OG002'}]}]}], 'paramType': 'MEAN', 'timeFrame': '1 month', 'description': "Sum score on Positive Reactions subscale of the Social Reactions Questionnaire - Shortened, completed by supporter in reference to supporter's reactions to survivor in past month. Range: 0 to 16; higher scores indicate more frequent positive reactions.", 'unitOfMeasure': 'score on a scale', 'dispersionType': 'Standard Error', 'reportingStatus': 'POSTED', 'populationDescription': 'Only assessed among supporters reporting past-month receipt of disclosure from the survivor'}, {'type': 'OTHER_PRE_SPECIFIED', 'title': 'Survivor Perceived Cultural Responsiveness of Intervention at 1 Month Post-baseline (Self Report)', 'denoms': [{'units': 'Participants', 'counts': [{'value': '19', 'groupId': 'OG000'}, {'value': '21', 'groupId': 'OG001'}]}], 'groups': [{'id': 'OG000', 'title': 'Dyadic CARE (Survivors)', 'description': 'Survivors randomized to receive dyadic CARE (both dyad members attended both sessions and completed a workbook together)'}, {'id': 'OG001', 'title': 'Supporter-Only CARE (Survivors)', 'description': 'Survivors randomized to receive supporter-only CARE (only the supporter attended both sessions; the dyad completed a workbook together)'}], 'classes': [{'categories': [{'measurements': [{'value': '9.84', 'spread': '1.74', 'groupId': 'OG000'}, {'value': '10.19', 'spread': '1.99', 'groupId': 'OG001'}]}]}], 'paramType': 'MEAN', 'timeFrame': '1 month', 'description': 'Sum score on survey created for this study, completed by survivor. Range: 4 to 16; higher scores indicate greater perceived cultural responsiveness of intervention.', 'unitOfMeasure': 'score on a scale', 'dispersionType': 'Standard Deviation', 'reportingStatus': 'POSTED', 'populationDescription': 'Participants were excluded if they did not complete this scale.'}, {'type': 'OTHER_PRE_SPECIFIED', 'title': 'Supporter Perceived Cultural Responsiveness of Intervention at 1 Month Post-baseline (Self Report)', 'denoms': [{'units': 'Participants', 'counts': [{'value': '20', 'groupId': 'OG000'}, {'value': '20', 'groupId': 'OG001'}]}], 'groups': [{'id': 'OG000', 'title': 'Dyadic CARE (Supporters)', 'description': 'Supporters randomized to receive dyadic CARE (both dyad members attended both sessions and completed a workbook together)'}, {'id': 'OG001', 'title': 'Supporter-Only CARE (Supporters)', 'description': 'Supporters randomized to receive supporter-only CARE (only the supporter attended both sessions; the dyad completed a workbook together)'}], 'classes': [{'categories': [{'measurements': [{'value': '10.35', 'spread': '1.84', 'groupId': 'OG000'}, {'value': '10.45', 'spread': '1.76', 'groupId': 'OG001'}]}]}], 'paramType': 'MEAN', 'timeFrame': '1 month', 'description': 'Sum score on survey created for this study, completed by survivor. Range: 4 to 16; higher scores indicate greater perceived cultural responsiveness of intervention.', 'unitOfMeasure': 'score on a scale', 'dispersionType': 'Standard Deviation', 'reportingStatus': 'POSTED', 'populationDescription': 'Participants were excluded if they did not complete this scale.'}, {'type': 'OTHER_PRE_SPECIFIED', 'title': 'Survivor Perceived Impact of Intervention at 1 Month Post-baseline (Self-report)', 'denoms': [{'units': 'Participants', 'counts': [{'value': '18', 'groupId': 'OG000'}, {'value': '21', 'groupId': 'OG001'}]}], 'groups': [{'id': 'OG000', 'title': 'Dyadic CARE (Survivors)', 'description': 'Survivors randomized to receive dyadic CARE (both dyad members attended both sessions and completed a workbook together)'}, {'id': 'OG001', 'title': 'Supporter-Only CARE (Survivors)', 'description': 'Survivors randomized to receive supporter-only CARE (only the supporter attended both sessions; the dyad completed a workbook together)'}], 'classes': [{'categories': [{'measurements': [{'value': '16.56', 'spread': '2.50', 'groupId': 'OG000'}, {'value': '15.71', 'spread': '2.37', 'groupId': 'OG001'}]}]}], 'paramType': 'MEAN', 'timeFrame': '1 month', 'description': 'Sum score on survey created for this study, completed by survivor. Range: 4 to 20; higher scores indicate greater perceived impact of intervention.', 'unitOfMeasure': 'score on a scale', 'dispersionType': 'Standard Deviation', 'reportingStatus': 'POSTED', 'populationDescription': 'Participants were excluded if they did not complete this scale.'}, {'type': 'OTHER_PRE_SPECIFIED', 'title': 'Supporter Perceived Impact of Intervention at 1 Month Post-baseline (Self-report)', 'denoms': [{'units': 'Participants', 'counts': [{'value': '20', 'groupId': 'OG000'}, {'value': '20', 'groupId': 'OG001'}]}], 'groups': [{'id': 'OG000', 'title': 'Dyadic CARE (Supporters)', 'description': 'Supporters randomized to receive dyadic CARE (both dyad members attended both sessions and completed a workbook together)'}, {'id': 'OG001', 'title': 'Supporter-Only CARE (Supporters)', 'description': 'Supporters randomized to receive supporter-only CARE (only the supporter attended both sessions; the dyad completed a workbook together)'}], 'classes': [{'categories': [{'measurements': [{'value': '16.80', 'spread': '2.53', 'groupId': 'OG000'}, {'value': '16.60', 'spread': '2.19', 'groupId': 'OG001'}]}]}], 'paramType': 'MEAN', 'timeFrame': '1 month', 'description': 'Sum score on survey created for this study, completed by supporter. Range: 4 to 20; higher scores indicate greater perceived impact of intervention.', 'unitOfMeasure': 'score on a scale', 'dispersionType': 'Standard Deviation', 'reportingStatus': 'POSTED', 'populationDescription': 'Participants were excluded if they did not complete this scale.'}, {'type': 'OTHER_PRE_SPECIFIED', 'title': 'Change in Supporter Typical Alcohol Consumption (Quantity) at 3 Months Post-baseline (Self Report)', 'denoms': [{'units': 'Participants', 'counts': [{'value': '20', 'groupId': 'OG000'}, {'value': '18', 'groupId': 'OG001'}, {'value': '19', 'groupId': 'OG002'}]}], 'groups': [{'id': 'OG000', 'title': 'Dyadic CARE (Supporters)', 'description': 'Supporters randomized to receive dyadic CARE (both dyad members attended both sessions and completed a workbook together)'}, {'id': 'OG001', 'title': 'Supporter-Only CARE (Supporters)', 'description': 'Supporters randomized to receive supporter-only CARE (only the supporter attended both sessions; the dyad completed a workbook together)'}, {'id': 'OG002', 'title': 'Waitlist Control (Supporters)', 'description': "Supporters randomized to receive waitlist CARE (invited to complete the CARE version of the survivor's choice following the completion of study measures)"}], 'classes': [{'categories': [{'measurements': [{'value': '0.25', 'spread': '2.59', 'groupId': 'OG000'}, {'value': '-0.78', 'spread': '1.48', 'groupId': 'OG001'}, {'value': '-1.87', 'spread': '5.99', 'groupId': 'OG002'}]}]}], 'paramType': 'MEAN', 'timeFrame': 'Baseline, 3 months', 'description': 'Number of typical drinks per week in past month reported by supporter on the Daily Drinking Questionnaire. Range: 0 to 7.', 'unitOfMeasure': 'Drinks Per Week', 'dispersionType': 'Standard Deviation', 'reportingStatus': 'POSTED', 'populationDescription': 'Because this is a change score, participants were excluded listwise if they had missing data at one or both assessments.'}, {'type': 'OTHER_PRE_SPECIFIED', 'title': 'Change in Supporter Typical Alcohol Consumption (Frequency) at 3 Months Post-baseline (Self Report)', 'denoms': [{'units': 'Participants', 'counts': [{'value': '20', 'groupId': 'OG000'}, {'value': '18', 'groupId': 'OG001'}, {'value': '19', 'groupId': 'OG002'}]}], 'groups': [{'id': 'OG000', 'title': 'Dyadic CARE (Supporters)', 'description': 'Supporters randomized to receive dyadic CARE (both dyad members attended both sessions and completed a workbook together)'}, {'id': 'OG001', 'title': 'Supporter-Only CARE (Supporters)', 'description': 'Supporters randomized to receive supporter-only CARE (only the supporter attended both sessions; the dyad completed a workbook together)'}, {'id': 'OG002', 'title': 'Waitlist Control (Supporters)', 'description': "Supporters randomized to receive waitlist CARE (invited to complete the CARE version of the survivor's choice following the completion of study measures)"}], 'classes': [{'categories': [{'measurements': [{'value': '0.05', 'spread': '0.83', 'groupId': 'OG000'}, {'value': '-0.22', 'spread': '0.69', 'groupId': 'OG001'}, {'value': '-0.21', 'spread': '1.32', 'groupId': 'OG002'}]}]}], 'paramType': 'MEAN', 'timeFrame': 'Baseline, 3 months', 'description': 'Number of typical drinking days per week in past month reported by supporter on the Daily Drinking Questionnaire. Range: 0 to 7.', 'unitOfMeasure': 'Days Per Week', 'dispersionType': 'Standard Deviation', 'reportingStatus': 'POSTED', 'populationDescription': 'Because this is a change score, participants were excluded listwise if they had missing data at one or both assessments.'}, {'type': 'OTHER_PRE_SPECIFIED', 'title': 'Change in Supporter Typical Alcohol Consumption (Hours) at 3 Months Post-baseline (Self Report)', 'denoms': [{'units': 'Participants', 'counts': [{'value': '20', 'groupId': 'OG000'}, {'value': '18', 'groupId': 'OG001'}, {'value': '19', 'groupId': 'OG002'}]}], 'groups': [{'id': 'OG000', 'title': 'Dyadic CARE (Supporters)', 'description': 'Supporters randomized to receive dyadic CARE (both dyad members attended both sessions and completed a workbook together)'}, {'id': 'OG001', 'title': 'Supporter-Only CARE (Supporters)', 'description': 'Supporters randomized to receive supporter-only CARE (only the supporter attended both sessions; the dyad completed a workbook together)'}, {'id': 'OG002', 'title': 'Waitlist Control (Supporters)', 'description': "Supporters randomized to receive waitlist CARE (invited to complete the CARE version of the survivor's choice following the completion of study measures)"}], 'classes': [{'categories': [{'measurements': [{'value': '2.30', 'spread': '8.90', 'groupId': 'OG000'}, {'value': '-0.89', 'spread': '2.03', 'groupId': 'OG001'}, {'value': '-1.26', 'spread': '7.09', 'groupId': 'OG002'}]}]}], 'paramType': 'MEAN', 'timeFrame': 'Baseline, 3 months', 'description': 'Number of typical drinking hours per week in past month reported by supporter on the Daily Drinking Questionnaire.', 'unitOfMeasure': 'Hours Per Week', 'dispersionType': 'Standard Deviation', 'reportingStatus': 'POSTED', 'populationDescription': 'Because this is a change score, participants were excluded listwise if they had missing data at one or both assessments.'}, {'type': 'OTHER_PRE_SPECIFIED', 'title': 'Change in Supporter Cannabis Use Frequency at 3 Months Post-baseline (Self Report)', 'denoms': [{'units': 'Participants', 'counts': [{'value': '20', 'groupId': 'OG000'}, {'value': '18', 'groupId': 'OG001'}, {'value': '20', 'groupId': 'OG002'}]}], 'groups': [{'id': 'OG000', 'title': 'Dyadic CARE (Supporters)', 'description': 'Supporters randomized to receive dyadic CARE (both dyad members attended both sessions and completed a workbook together)'}, {'id': 'OG001', 'title': 'Supporter-Only CARE (Supporters)', 'description': 'Supporters randomized to receive supporter-only CARE (only the supporter attended both sessions; the dyad completed a workbook together)'}, {'id': 'OG002', 'title': 'Waitlist Control (Supporters)', 'description': "Supporters randomized to receive waitlist CARE (invited to complete the CARE version of the survivor's choice following the completion of study measures)"}], 'classes': [{'categories': [{'measurements': [{'value': '0.45', 'spread': '1.88', 'groupId': 'OG000'}, {'value': '-0.11', 'spread': '0.32', 'groupId': 'OG001'}, {'value': '-0.85', 'spread': '3.56', 'groupId': 'OG002'}]}]}], 'paramType': 'MEAN', 'timeFrame': 'Baseline, 3 months', 'description': 'Number of days of cannabis use in past 2 weeks, as reported by supporter. Range: 0 to 14.', 'unitOfMeasure': 'Days', 'dispersionType': 'Standard Deviation', 'reportingStatus': 'POSTED', 'populationDescription': 'Because this is a change score, participants were excluded listwise if they had missing data at one or both assessments.'}, {'type': 'OTHER_PRE_SPECIFIED', 'title': 'Change in Supporter Prescription Opioid Misuse Frequency at 3 Months Post-baseline (Self Report)', 'denoms': [{'units': 'Participants', 'counts': [{'value': '0', 'groupId': 'OG000'}, {'value': '0', 'groupId': 'OG001'}, {'value': '0', 'groupId': 'OG002'}]}], 'groups': [{'id': 'OG000', 'title': 'Dyadic CARE (Supporters)', 'description': 'Supporters randomized to receive dyadic CARE (both dyad members attended both sessions and completed a workbook together)'}, {'id': 'OG001', 'title': 'Supporter-Only CARE (Supporters)', 'description': 'Supporters randomized to receive supporter-only CARE (only the supporter attended both sessions; the dyad completed a workbook together)'}, {'id': 'OG002', 'title': 'Waitlist Control (Supporters)', 'description': "Supporters randomized to receive waitlist CARE (invited to complete the CARE version of the survivor's choice following the completion of study measures)"}], 'timeFrame': 'Baseline, 3 months', 'description': 'Number of days of prescription opioid use not as prescribed in past 2 weeks, as reported by supporter. Range: 0 to 14.', 'reportingStatus': 'POSTED', 'populationDescription': 'It was not possible to compute change scores because no participants reported prescription opioid use at any assessment'}, {'type': 'OTHER_PRE_SPECIFIED', 'title': 'Change in Supporter Non-prescription Opioid Use Frequency at 3 Months Post-baseline (Self Report)', 'denoms': [{'units': 'Participants', 'counts': [{'value': '0', 'groupId': 'OG000'}, {'value': '0', 'groupId': 'OG001'}, {'value': '0', 'groupId': 'OG002'}]}], 'groups': [{'id': 'OG000', 'title': 'Dyadic CARE (Supporters)', 'description': 'Supporters randomized to receive dyadic CARE (both dyad members attended both sessions and completed a workbook together)'}, {'id': 'OG001', 'title': 'Supporter-Only CARE (Supporters)', 'description': 'Supporters randomized to receive supporter-only CARE (only the supporter attended both sessions; the dyad completed a workbook together)'}, {'id': 'OG002', 'title': 'Waitlist Control (Supporters)', 'description': "Supporters randomized to receive waitlist CARE (invited to complete the CARE version of the survivor's choice following the completion of study measures)"}], 'timeFrame': 'Baseline, 3 months', 'description': 'Number of days of non-prescription opioid use in past 2 weeks, as reported by supporter. Range: 0 to 14.', 'reportingStatus': 'POSTED', 'populationDescription': 'It was not possible to compute change scores because no participants reported non-prescription opioid use at any assessment'}, {'type': 'OTHER_PRE_SPECIFIED', 'title': 'Change in Supporter Prescription Amphetamine Misuse Frequency at 3 Months Post-baseline (Self Report)', 'denoms': [{'units': 'Participants', 'counts': [{'value': '0', 'groupId': 'OG000'}, {'value': '0', 'groupId': 'OG001'}, {'value': '0', 'groupId': 'OG002'}]}], 'groups': [{'id': 'OG000', 'title': 'Dyadic CARE (Supporters)', 'description': 'Supporters randomized to receive dyadic CARE (both dyad members attended both sessions and completed a workbook together)'}, {'id': 'OG001', 'title': 'Supporter-Only CARE (Supporters)', 'description': 'Supporters randomized to receive supporter-only CARE (only the supporter attended both sessions; the dyad completed a workbook together)'}, {'id': 'OG002', 'title': 'Waitlist Control (Supporters)', 'description': "Supporters randomized to receive waitlist CARE (invited to complete the CARE version of the survivor's choice following the completion of study measures)"}], 'timeFrame': 'Baseline, 3 months', 'description': 'Number of days of prescription amphetamine use not as prescribed in past 2 weeks, as reported by supporter. Range: 0 to 14.', 'reportingStatus': 'POSTED', 'populationDescription': 'It was not possible to compute change scores because amphetamine use was very low base rate'}, {'type': 'OTHER_PRE_SPECIFIED', 'title': 'Change in Supporter Methamphetamine Use Frequency at 3 Months Post-baseline (Self Report)', 'denoms': [{'units': 'Participants', 'counts': [{'value': '0', 'groupId': 'OG000'}, {'value': '0', 'groupId': 'OG001'}, {'value': '0', 'groupId': 'OG002'}]}], 'groups': [{'id': 'OG000', 'title': 'Dyadic CARE (Supporters)', 'description': 'Supporters randomized to receive dyadic CARE (both dyad members attended both sessions and completed a workbook together)'}, {'id': 'OG001', 'title': 'Supporter-Only CARE (Supporters)', 'description': 'Supporters randomized to receive supporter-only CARE (only the supporter attended both sessions; the dyad completed a workbook together)'}, {'id': 'OG002', 'title': 'Waitlist Control (Supporters)', 'description': "Supporters randomized to receive waitlist CARE (invited to complete the CARE version of the survivor's choice following the completion of study measures)"}], 'timeFrame': 'Baseline, 3 months', 'description': 'Number of days of methamphetamine use in past 2 weeks, as reported by supporter. Range: 0 to 14.', 'reportingStatus': 'POSTED', 'populationDescription': 'It was not possible to compute change scores because no participants reported methamphetamine use at any assessment'}, {'type': 'OTHER_PRE_SPECIFIED', 'title': 'Change in Supporter Cigarette Use Frequency at 3 Months Post-baseline (Self Report)', 'denoms': [{'units': 'Participants', 'counts': [{'value': '20', 'groupId': 'OG000'}, {'value': '0', 'groupId': 'OG001'}, {'value': '20', 'groupId': 'OG002'}]}], 'groups': [{'id': 'OG000', 'title': 'Dyadic CARE (Supporters)', 'description': 'Supporters randomized to receive dyadic CARE (both dyad members attended both sessions and completed a workbook together)'}, {'id': 'OG001', 'title': 'Supporter-Only CARE (Supporters)', 'description': 'Supporters randomized to receive supporter-only CARE (only the supporter attended both sessions; the dyad completed a workbook together)'}, {'id': 'OG002', 'title': 'Waitlist Control (Supporters)', 'description': "Supporters randomized to receive waitlist CARE (invited to complete the CARE version of the survivor's choice following the completion of study measures)"}], 'classes': [{'categories': [{'measurements': [{'value': '-0.10', 'spread': '0.31', 'groupId': 'OG000'}, {'value': '-0.15', 'spread': '2.37', 'groupId': 'OG002'}]}]}], 'paramType': 'MEAN', 'timeFrame': 'Baseline, 3 months', 'description': 'Number of days of cigarette use in past 2 weeks, as reported by supporter. Range: 0 to 14.', 'unitOfMeasure': 'Days', 'dispersionType': 'Standard Deviation', 'reportingStatus': 'POSTED', 'populationDescription': 'Because this is a change score, participants were excluded listwise if they had missing data at one or both assessments. It was not possible to compute change scores for the Supporter-only condition because no participants reported cigarette use.'}, {'type': 'OTHER_PRE_SPECIFIED', 'title': 'Change in Supporter Cigarette Use Quantity at 3 Months Post-baseline (Self Report)', 'denoms': [{'units': 'Participants', 'counts': [{'value': '20', 'groupId': 'OG000'}, {'value': '0', 'groupId': 'OG001'}, {'value': '20', 'groupId': 'OG002'}]}], 'groups': [{'id': 'OG000', 'title': 'Dyadic CARE (Supporters)', 'description': 'Supporters randomized to receive dyadic CARE (both dyad members attended both sessions and completed a workbook together)'}, {'id': 'OG001', 'title': 'Supporter-Only CARE (Supporters)', 'description': 'Supporters randomized to receive supporter-only CARE (only the supporter attended both sessions; the dyad completed a workbook together)'}, {'id': 'OG002', 'title': 'Waitlist Control (Supporters)', 'description': "Supporters randomized to receive waitlist CARE (invited to complete the CARE version of the survivor's choice following the completion of study measures)"}], 'classes': [{'categories': [{'measurements': [{'value': '-0.05', 'spread': '0.22', 'groupId': 'OG000'}, {'value': '-0.18', 'spread': '1.16', 'groupId': 'OG002'}]}]}], 'paramType': 'MEAN', 'timeFrame': 'Baseline, 3 months', 'description': 'Number of cigarettes smoked in a typical day in past 2 weeks, as reported by supporter.', 'unitOfMeasure': 'Cigarettes Per Day', 'dispersionType': 'Standard Deviation', 'reportingStatus': 'POSTED', 'populationDescription': 'Because this is a change score, participants were excluded listwise if they had missing data at one or both assessments. It was not possible to compute change scores for the Supporter-only condition because no participants reported cigarette use.'}]}, 'participantFlowModule': {'groups': [{'id': 'FG000', 'title': 'Dyadic CARE', 'description': 'Dyads randomized to receive dyadic CARE. Dyadic CARE involved both dyad members attending 2 sessions and completing a workbook together. Session 1 typically occurred immediately following baseline/randomization (maximum: 2 weeks later). Session 2 typically occurred 2 weeks after Session 1 (maximum: 4 weeks later).'}, {'id': 'FG001', 'title': 'Supporter-Only CARE', 'description': 'Dyads randomized to receive supporter-only CARE. Supporter-only CARE involved the supporter attending 2 sessions and completing a workbook with the survivor. Session 1 typically occurred immediately following baseline/randomization (maximum: 2 weeks later). Session 2 typically occurred 2 weeks after Session 1 (maximum: 4 weeks later).'}, {'id': 'FG002', 'title': 'Waitlist Control', 'description': "Dyads randomized to receive waitlist CARE (invited to complete the CARE version of the survivor's choice following the completion of study measures)"}], 'periods': [{'title': 'Overall Study', 'milestones': [{'type': 'STARTED', 'achievements': [{'comment': '21 survivors and 21 supporters started', 'groupId': 'FG000', 'numSubjects': '42'}, {'comment': '22 survivors and 22 supporters started', 'groupId': 'FG001', 'numSubjects': '44'}, {'comment': '21 survivors and 21 supporters started', 'groupId': 'FG002', 'numSubjects': '42'}]}, {'type': 'COMPLETED', 'achievements': [{'comment': '20 survivors and 20 supporters completed', 'groupId': 'FG000', 'numSubjects': '40'}, {'comment': '21 survivors and 21 supporters completed', 'groupId': 'FG001', 'numSubjects': '42'}, {'comment': '21 survivors and 20 supporters completed', 'groupId': 'FG002', 'numSubjects': '41'}]}, {'type': 'NOT COMPLETED', 'achievements': [{'groupId': 'FG000', 'numSubjects': '2'}, {'groupId': 'FG001', 'numSubjects': '2'}, {'groupId': 'FG002', 'numSubjects': '1'}]}], 'dropWithdraws': [{'type': 'Withdrawal by Subject', 'reasons': [{'groupId': 'FG000', 'numSubjects': '2'}, {'groupId': 'FG001', 'numSubjects': '0'}, {'groupId': 'FG002', 'numSubjects': '0'}]}, {'type': 'Did not meet eligibility criteria', 'reasons': [{'groupId': 'FG000', 'numSubjects': '0'}, {'groupId': 'FG001', 'numSubjects': '2'}, {'groupId': 'FG002', 'numSubjects': '0'}]}, {'type': 'Lost to Follow-up', 'reasons': [{'groupId': 'FG000', 'numSubjects': '0'}, {'groupId': 'FG001', 'numSubjects': '0'}, {'groupId': 'FG002', 'numSubjects': '1'}]}]}]}, 'baselineCharacteristicsModule': {'denoms': [{'units': 'Participants', 'counts': [{'value': '21', 'groupId': 'BG000'}, {'value': '22', 'groupId': 'BG001'}, {'value': '21', 'groupId': 'BG002'}, {'value': '21', 'groupId': 'BG003'}, {'value': '22', 'groupId': 'BG004'}, {'value': '21', 'groupId': 'BG005'}, {'value': '128', 'groupId': 'BG006'}]}], 'groups': [{'id': 'BG000', 'title': 'Dyadic CARE (Survivors)', 'description': 'Survivors randomized to receive dyadic CARE (both dyad members attended both sessions and completed a workbook together)'}, {'id': 'BG001', 'title': 'Supporter-Only CARE (Survivors)', 'description': 'Survivors randomized to receive supporter-only CARE (only the supporter attended both sessions; the dyad completed a workbook together)'}, {'id': 'BG002', 'title': 'Waitlist Control (Survivors)', 'description': 'Survivors randomized to receive waitlist CARE (invited to complete the CARE version of their choice following the completion of study measures)'}, {'id': 'BG003', 'title': 'Dyadic CARE (Supporters)', 'description': 'Supporters randomized to receive dyadic CARE (both dyad members attended both sessions and completed a workbook together)'}, {'id': 'BG004', 'title': 'Supporter-Only CARE (Supporters)', 'description': 'Supporters randomized to receive supporter-only CARE (only the supporter attended both sessions; the dyad completed a workbook together)'}, {'id': 'BG005', 'title': 'Waitlist Control (Supporters)', 'description': "Supporters randomized to receive waitlist CARE (invited to complete the CARE version of the survivor's choice following the completion of study measures)"}, {'id': 'BG006', 'title': 'Total', 'description': 'Total of all reporting groups'}], 'measures': [{'title': 'Age, Continuous', 'classes': [{'denoms': [{'units': 'Participants', 'counts': [{'value': '21', 'groupId': 'BG000'}, {'value': '21', 'groupId': 'BG001'}, {'value': '21', 'groupId': 'BG002'}, {'value': '21', 'groupId': 'BG003'}, {'value': '21', 'groupId': 'BG004'}, {'value': '20', 'groupId': 'BG005'}, {'value': '125', 'groupId': 'BG006'}]}], 'categories': [{'measurements': [{'value': '26.48', 'spread': '9.56', 'groupId': 'BG000'}, {'value': '23.24', 'spread': '6.07', 'groupId': 'BG001'}, {'value': '25.52', 'spread': '9.32', 'groupId': 'BG002'}, {'value': '32.48', 'spread': '10.75', 'groupId': 'BG003'}, {'value': '37.52', 'spread': '15.38', 'groupId': 'BG004'}, {'value': '30.80', 'spread': '11.87', 'groupId': 'BG005'}, {'value': '29.33', 'spread': '11.69', 'groupId': 'BG006'}]}]}], 'paramType': 'MEAN', 'unitOfMeasure': 'Years', 'dispersionType': 'STANDARD_DEVIATION', 'populationDescription': 'One participant did not report their age. Two participants were withdrawn by researchers for not meeting eligibility and were not included in analyses.'}, {'title': 'Sex: Female, Male', 'classes': [{'denoms': [{'units': 'Participants', 'counts': [{'value': '20', 'groupId': 'BG000'}, {'value': '21', 'groupId': 'BG001'}, {'value': '21', 'groupId': 'BG002'}, {'value': '21', 'groupId': 'BG003'}, {'value': '21', 'groupId': 'BG004'}, {'value': '21', 'groupId': 'BG005'}, {'value': '125', 'groupId': 'BG006'}]}], 'categories': [{'title': 'Female', 'measurements': [{'value': '19', 'groupId': 'BG000'}, {'value': '18', 'groupId': 'BG001'}, {'value': '20', 'groupId': 'BG002'}, {'value': '13', 'groupId': 'BG003'}, {'value': '16', 'groupId': 'BG004'}, {'value': '16', 'groupId': 'BG005'}, {'value': '102', 'groupId': 'BG006'}]}, {'title': 'Male', 'measurements': [{'value': '1', 'groupId': 'BG000'}, {'value': '3', 'groupId': 'BG001'}, {'value': '1', 'groupId': 'BG002'}, {'value': '8', 'groupId': 'BG003'}, {'value': '5', 'groupId': 'BG004'}, {'value': '5', 'groupId': 'BG005'}, {'value': '23', 'groupId': 'BG006'}]}]}], 'paramType': 'COUNT_OF_PARTICIPANTS', 'calculatePct': False, 'unitOfMeasure': 'Participants', 'populationDescription': 'One participant did not report sex. Two participants were withdrawn by researchers for not meeting eligibility and were not included in analyses.'}, {'title': 'Ethnicity (NIH/OMB)', 'classes': [{'denoms': [{'units': 'Participants', 'counts': [{'value': '21', 'groupId': 'BG000'}, {'value': '21', 'groupId': 'BG001'}, {'value': '21', 'groupId': 'BG002'}, {'value': '21', 'groupId': 'BG003'}, {'value': '21', 'groupId': 'BG004'}, {'value': '21', 'groupId': 'BG005'}, {'value': '126', 'groupId': 'BG006'}]}], 'categories': [{'title': 'Hispanic or Latino', 'measurements': [{'value': '4', 'groupId': 'BG000'}, {'value': '5', 'groupId': 'BG001'}, {'value': '4', 'groupId': 'BG002'}, {'value': '17', 'groupId': 'BG003'}, {'value': '18', 'groupId': 'BG004'}, {'value': '18', 'groupId': 'BG005'}, {'value': '66', 'groupId': 'BG006'}]}, {'title': 'Not Hispanic or Latino', 'measurements': [{'value': '17', 'groupId': 'BG000'}, {'value': '16', 'groupId': 'BG001'}, {'value': '17', 'groupId': 'BG002'}, {'value': '4', 'groupId': 'BG003'}, {'value': '3', 'groupId': 'BG004'}, {'value': '3', 'groupId': 'BG005'}, {'value': '60', 'groupId': 'BG006'}]}, {'title': 'Unknown or Not Reported', 'measurements': [{'value': '0', 'groupId': 'BG000'}, {'value': '0', 'groupId': 'BG001'}, {'value': '0', 'groupId': 'BG002'}, {'value': '0', 'groupId': 'BG003'}, {'value': '0', 'groupId': 'BG004'}, {'value': '0', 'groupId': 'BG005'}, {'value': '0', 'groupId': 'BG006'}]}]}], 'paramType': 'COUNT_OF_PARTICIPANTS', 'calculatePct': False, 'unitOfMeasure': 'Participants', 'populationDescription': 'Two participants were withdrawn by researchers for not meeting eligibility and were not included in analyses.'}, {'title': 'Race (NIH/OMB)', 'classes': [{'denoms': [{'units': 'Participants', 'counts': [{'value': '21', 'groupId': 'BG000'}, {'value': '21', 'groupId': 'BG001'}, {'value': '21', 'groupId': 'BG002'}, {'value': '21', 'groupId': 'BG003'}, {'value': '21', 'groupId': 'BG004'}, {'value': '21', 'groupId': 'BG005'}, {'value': '126', 'groupId': 'BG006'}]}], 'categories': [{'title': 'American Indian or Alaska Native', 'measurements': [{'value': '0', 'groupId': 'BG000'}, {'value': '1', 'groupId': 'BG001'}, {'value': '0', 'groupId': 'BG002'}, {'value': '0', 'groupId': 'BG003'}, {'value': '0', 'groupId': 'BG004'}, {'value': '0', 'groupId': 'BG005'}, {'value': '1', 'groupId': 'BG006'}]}, {'title': 'Asian', 'measurements': [{'value': '5', 'groupId': 'BG000'}, {'value': '6', 'groupId': 'BG001'}, {'value': '4', 'groupId': 'BG002'}, {'value': '5', 'groupId': 'BG003'}, {'value': '6', 'groupId': 'BG004'}, {'value': '4', 'groupId': 'BG005'}, {'value': '30', 'groupId': 'BG006'}]}, {'title': 'Native Hawaiian or Other Pacific Islander', 'measurements': [{'value': '0', 'groupId': 'BG000'}, {'value': '0', 'groupId': 'BG001'}, {'value': '0', 'groupId': 'BG002'}, {'value': '0', 'groupId': 'BG003'}, {'value': '0', 'groupId': 'BG004'}, {'value': '0', 'groupId': 'BG005'}, {'value': '0', 'groupId': 'BG006'}]}, {'title': 'Black or African American', 'measurements': [{'value': '1', 'groupId': 'BG000'}, {'value': '0', 'groupId': 'BG001'}, {'value': '0', 'groupId': 'BG002'}, {'value': '2', 'groupId': 'BG003'}, {'value': '0', 'groupId': 'BG004'}, {'value': '1', 'groupId': 'BG005'}, {'value': '4', 'groupId': 'BG006'}]}, {'title': 'White', 'measurements': [{'value': '7', 'groupId': 'BG000'}, {'value': '8', 'groupId': 'BG001'}, {'value': '12', 'groupId': 'BG002'}, {'value': '9', 'groupId': 'BG003'}, {'value': '10', 'groupId': 'BG004'}, {'value': '13', 'groupId': 'BG005'}, {'value': '59', 'groupId': 'BG006'}]}, {'title': 'More than one race', 'measurements': [{'value': '5', 'groupId': 'BG000'}, {'value': '3', 'groupId': 'BG001'}, {'value': '3', 'groupId': 'BG002'}, {'value': '2', 'groupId': 'BG003'}, {'value': '1', 'groupId': 'BG004'}, {'value': '0', 'groupId': 'BG005'}, {'value': '14', 'groupId': 'BG006'}]}, {'title': 'Unknown or Not Reported', 'measurements': [{'value': '3', 'groupId': 'BG000'}, {'value': '3', 'groupId': 'BG001'}, {'value': '2', 'groupId': 'BG002'}, {'value': '3', 'groupId': 'BG003'}, {'value': '4', 'groupId': 'BG004'}, {'value': '3', 'groupId': 'BG005'}, {'value': '18', 'groupId': 'BG006'}]}]}], 'paramType': 'COUNT_OF_PARTICIPANTS', 'calculatePct': False, 'unitOfMeasure': 'Participants', 'populationDescription': 'Two participants were withdrawn by researchers for not meeting eligibility and were not included in analyses.'}]}}, 'documentSection': {'largeDocumentModule': {'largeDocs': [{'date': '2025-04-14', 'size': 1191953, 'label': 'Study Protocol, Statistical Analysis Plan, and Informed Consent Form', 'hasIcf': True, 'hasSap': True, 'filename': 'Prot_SAP_ICF_000.pdf', 'typeAbbrev': 'Prot_SAP_ICF', 'uploadDate': '2025-05-16T12:49', 'hasProtocol': True}]}}, 'protocolSection': {'designModule': {'phases': ['NA'], 'studyType': 'INTERVENTIONAL', 'designInfo': {'allocation': 'RANDOMIZED', 'maskingInfo': {'masking': 'NONE'}, 'primaryPurpose': 'PREVENTION', 'interventionModel': 'PARALLEL'}, 'enrollmentInfo': {'type': 'ACTUAL', 'count': 128}}, 'statusModule': {'overallStatus': 'COMPLETED', 'startDateStruct': {'date': '2022-05-18', 'type': 'ACTUAL'}, 'expandedAccessInfo': {'hasExpandedAccess': False}, 'statusVerifiedDate': '2025-06', 'completionDateStruct': {'date': '2024-07-04', 'type': 'ACTUAL'}, 'lastUpdateSubmitDate': '2025-06-05', 'studyFirstSubmitDate': '2022-04-06', 'resultsFirstSubmitDate': '2025-04-14', 'studyFirstSubmitQcDate': '2022-04-20', 'lastUpdatePostDateStruct': {'date': '2025-06-08', 'type': 'ACTUAL'}, 'resultsFirstSubmitQcDate': '2025-06-05', 'studyFirstPostDateStruct': {'date': '2022-04-25', 'type': 'ACTUAL'}, 'resultsFirstPostDateStruct': {'date': '2025-06-08', 'type': 'ACTUAL'}, 'primaryCompletionDateStruct': {'date': '2024-07-04', 'type': 'ACTUAL'}}, 'outcomesModule': {'otherOutcomes': [{'measure': 'Survivor Disclosure Frequency to Supporter at 1 Month Post-baseline (Informant Report)', 'timeFrame': '1 month', 'description': "Single item representing frequency of survivor's disclosures to supporter in past month, completed by supporter, adapted from the Early Intervention Clinic Disclosure Scale. Participants were instructed to enter a numerical value corresponding to number of disclosures. Higher scores indicate more frequent disclosure."}, {'measure': 'Supporter Negative Reactions to Disclosure at 1 Month Post-baseline (Self Report)', 'timeFrame': '1 month', 'description': "Sum score on Negative Reactions subscale of the Social Reactions Questionnaire - Shortened, completed by supporter in reference to supporter's reactions to survivor in past month. Range: 0 to 48; higher scores indicate more frequent negative reactions."}, {'measure': 'Supporter Positive Reactions to Disclosure at 1 Month Post-baseline (Self Report)', 'timeFrame': '1 month', 'description': "Sum score on Positive Reactions subscale of the Social Reactions Questionnaire - Shortened, completed by supporter in reference to supporter's reactions to survivor in past month. Range: 0 to 16; higher scores indicate more frequent positive reactions."}, {'measure': 'Survivor Perceived Cultural Responsiveness of Intervention at 1 Month Post-baseline (Self Report)', 'timeFrame': '1 month', 'description': 'Sum score on survey created for this study, completed by survivor. Range: 4 to 16; higher scores indicate greater perceived cultural responsiveness of intervention.'}, {'measure': 'Supporter Perceived Cultural Responsiveness of Intervention at 1 Month Post-baseline (Self Report)', 'timeFrame': '1 month', 'description': 'Sum score on survey created for this study, completed by survivor. Range: 4 to 16; higher scores indicate greater perceived cultural responsiveness of intervention.'}, {'measure': 'Survivor Perceived Impact of Intervention at 1 Month Post-baseline (Self-report)', 'timeFrame': '1 month', 'description': 'Sum score on survey created for this study, completed by survivor. Range: 4 to 20; higher scores indicate greater perceived impact of intervention.'}, {'measure': 'Supporter Perceived Impact of Intervention at 1 Month Post-baseline (Self-report)', 'timeFrame': '1 month', 'description': 'Sum score on survey created for this study, completed by supporter. Range: 4 to 20; higher scores indicate greater perceived impact of intervention.'}, {'measure': 'Change in Supporter Typical Alcohol Consumption (Quantity) at 3 Months Post-baseline (Self Report)', 'timeFrame': 'Baseline, 3 months', 'description': 'Number of typical drinks per week in past month reported by supporter on the Daily Drinking Questionnaire. Range: 0 to 7.'}, {'measure': 'Change in Supporter Typical Alcohol Consumption (Frequency) at 3 Months Post-baseline (Self Report)', 'timeFrame': 'Baseline, 3 months', 'description': 'Number of typical drinking days per week in past month reported by supporter on the Daily Drinking Questionnaire. Range: 0 to 7.'}, {'measure': 'Change in Supporter Typical Alcohol Consumption (Hours) at 3 Months Post-baseline (Self Report)', 'timeFrame': 'Baseline, 3 months', 'description': 'Number of typical drinking hours per week in past month reported by supporter on the Daily Drinking Questionnaire.'}, {'measure': 'Change in Supporter Cannabis Use Frequency at 3 Months Post-baseline (Self Report)', 'timeFrame': 'Baseline, 3 months', 'description': 'Number of days of cannabis use in past 2 weeks, as reported by supporter. Range: 0 to 14.'}, {'measure': 'Change in Supporter Prescription Opioid Misuse Frequency at 3 Months Post-baseline (Self Report)', 'timeFrame': 'Baseline, 3 months', 'description': 'Number of days of prescription opioid use not as prescribed in past 2 weeks, as reported by supporter. Range: 0 to 14.'}, {'measure': 'Change in Supporter Non-prescription Opioid Use Frequency at 3 Months Post-baseline (Self Report)', 'timeFrame': 'Baseline, 3 months', 'description': 'Number of days of non-prescription opioid use in past 2 weeks, as reported by supporter. Range: 0 to 14.'}, {'measure': 'Change in Supporter Prescription Amphetamine Misuse Frequency at 3 Months Post-baseline (Self Report)', 'timeFrame': 'Baseline, 3 months', 'description': 'Number of days of prescription amphetamine use not as prescribed in past 2 weeks, as reported by supporter. Range: 0 to 14.'}, {'measure': 'Change in Supporter Methamphetamine Use Frequency at 3 Months Post-baseline (Self Report)', 'timeFrame': 'Baseline, 3 months', 'description': 'Number of days of methamphetamine use in past 2 weeks, as reported by supporter. Range: 0 to 14.'}, {'measure': 'Change in Supporter Cigarette Use Frequency at 3 Months Post-baseline (Self Report)', 'timeFrame': 'Baseline, 3 months', 'description': 'Number of days of cigarette use in past 2 weeks, as reported by supporter. Range: 0 to 14.'}, {'measure': 'Change in Supporter Cigarette Use Quantity at 3 Months Post-baseline (Self Report)', 'timeFrame': 'Baseline, 3 months', 'description': 'Number of cigarettes smoked in a typical day in past 2 weeks, as reported by supporter.'}], 'primaryOutcomes': [{'measure': 'Survivor Satisfaction With Intervention at 1 Month Post-baseline (Self Report)', 'timeFrame': '1 month', 'description': 'Sum score on Client Satisfaction Scale, completed by survivor. Range: 8 to 32; higher scores indicate greater satisfaction'}, {'measure': 'Supporter Satisfaction With Intervention at 1 Month Post-baseline (Self Report)', 'timeFrame': '1 month', 'description': 'Sum score on Client Satisfaction Scale, completed by supporter. Range: 8 to 32; higher scores indicate greater satisfaction'}, {'measure': 'Change in Survivor Knowledge at 1 Month Post-baseline (Self Report)', 'timeFrame': 'Baseline, 1 month', 'description': 'Sum score on a knowledge questionnaire reflecting CARE concepts, completed by the survivor. Range: 8 to 40; higher scores indicate more knowledge about CARE concepts.'}, {'measure': 'Change in Supporter Knowledge at 1 Month Post-baseline (Self Report)', 'timeFrame': 'Baseline, 1 month', 'description': 'Sum score on a knowledge questionnaire reflecting CARE concepts, completed by the supporter. Range: 9 to 45; higher scores indicate more knowledge about CARE concepts.'}, {'measure': 'Change in Survivor Confusion About Help-seeking Behavior at 1 Month Post-baseline (Self Report)', 'timeFrame': 'Baseline, 1 month', 'description': 'Sum score on 4-item measure created for this study, completed by survivor. Range: 4 to 20; higher scores indicate greater confusion.'}, {'measure': 'Change in Supporter Confusion About Helping Behavior at 1 Month Post-baseline (Self Report)', 'timeFrame': 'Baseline, 1 month', 'description': 'Sum score on the Confusion subscale of the Impact on Friends scale, completed by supporter. Range: 6 to 30; higher scores indicate greater confusion about helping behavior.'}, {'measure': 'Survivor Disclosure Frequency to Supporter at 1 Month Post-baseline (Self Report)', 'timeFrame': '1 month', 'description': 'Single item representing frequency of disclosures to supporter in past month, completed by survivor, adapted from the Early Intervention Clinic Disclosure scale. Survivor will input a numerical response representing number of disclosures. Higher scores indicate more frequent disclosure.'}, {'measure': 'Supporter Overt Hostile Reactions to Disclosure at 1 Month Post-baseline (Informant Report)', 'timeFrame': '1 month', 'description': "Sum score on Turning Against subscale of the Social Reactions Questionnaire - Shortened, completed by survivor in reference to supporter's reactions in past month. Range: 0 to 24; higher scores indicate more frequent hostile negative reactions."}, {'measure': 'Supporter Subtly Unsupportive Reactions to Disclosure at 1 Month Post-baseline (Informant Report)', 'timeFrame': '1 month', 'description': "Sum score on Unsupportive Acknowledgment subscale of the Social Reactions Questionnaire - Shortened, completed by survivor in reference to supporter's reactions in past month. Range: 0 to 24; higher scores indicate more frequent subtly unsupportive reactions."}, {'measure': 'Change in Supporter Responsiveness at 1 Month Post-baseline (Informant Report)', 'timeFrame': 'Baseline & 1 month', 'description': 'Sum score on the Responsiveness subscale of the Perceived Responsiveness and Insensitivity scale, completed by survivor in reference to past month. Range: 0 to 40; higher scores indicate greater responsiveness.'}, {'measure': 'Change in Survivor PTSD Symptom Severity at 3 Months Post-baseline (Self Report)', 'timeFrame': 'Baseline, 3 months', 'description': 'Sum score on PTSD Checklist-5 (PCL-5), completed by survivor in reference to past month. Range: 0-80; higher scores indicate greater severity of PTSD symptoms.'}, {'measure': 'Survivor Provisional PTSD Diagnostic Status at 3 Months Post-baseline (Self Report)', 'timeFrame': '3 months', 'description': 'Provisional PTSD diagnostic status based on PTSD Checklist-5 (PCL-5), completed by survivor in reference to past month. Survivors will be considered to have a provisional diagnosis if the following items are rated as 2 = "Moderately" or higher: one Criterion B item (questions 1-5), one Criterion C item (questions 6-7), two Criterion D items (questions 8-14), and two Criterion E items (questions 15-20).'}, {'measure': 'Change in Survivor Stress at 3 Months Post-baseline (Self Report)', 'timeFrame': 'Baseline, 3 months', 'description': 'Sum score on the Stress subscale of the Depression and Anxiety Stress Scales (DASS-21), completed by survivor in reference to past week. Range: 0 to 21; higher scores indicate greater stress.'}, {'measure': 'Change in Supporter Stress at 3 Months Post-baseline (Self Report)', 'timeFrame': 'Baseline, 3 months', 'description': 'Sum score on the Stress subscale of the Depression and Anxiety Stress Scales (DASS-21), completed by supporter in reference to past week. Range: 0 to 21; higher scores indicate greater stress.'}, {'measure': 'Change in Survivor Perceived Relationship Quality at 3 Months Post-baseline (Self Report)', 'timeFrame': 'Baseline, 3 months', 'description': 'Sum score on the Relationship Assessment Scale, completed by survivor. Range: 7 to 35; higher scores indicate greater relationship quality.'}, {'measure': 'Change in Supporter Perceived Relationship Quality at 3 Months Post-baseline (Self Report)', 'timeFrame': 'Baseline, 3 months', 'description': 'Sum score on the Relationship Assessment Scale, completed by supporter. Range: 7 to 35; higher scores indicate greater relationship quality.'}], 'secondaryOutcomes': [{'measure': 'Survivor Willingness to Participate in Criminal Justice Process at 1 Month Post-baseline (Self Report)', 'timeFrame': '1 month', 'description': 'Sum score score on measure created for this study, completed by survivor. Range: 0 to 10; higher scores indicate greater willingness.'}, {'measure': 'Survivor Participation in Criminal Justice Process at 1 Month Post-baseline (Self Report)', 'timeFrame': '1 month', 'description': 'Mean score on measure created for this study, completed by survivor. Range: 0 to 1; higher scores indicate greater participation.'}, {'measure': 'Change in Survivor Depression at 3 Months Post-baseline (Self Report)', 'timeFrame': 'Baseline, 3 months', 'description': 'Sum score on the Depression subscale of the Depression and Anxiety Stress Scales (DASS-21), completed by survivor in reference to past week. Range: 0 to 21; higher scores indicate greater depression.'}, {'measure': 'Change in Supporter Depression at 3 Months Post-baseline (Self Report)', 'timeFrame': 'Baseline, 3 months', 'description': 'Sum score on the Depression subscale of the Depression and Anxiety Stress Scales (DASS-21), completed by supporter in reference to past week. Range: 0 to 21; higher scores indicate greater depression.'}, {'measure': 'Change in Survivor Anxiety at 3 Months Post-baseline (Self Report)', 'timeFrame': 'Baseline, 3 months', 'description': 'Sum score on the Anxiety subscale of the Depression and Anxiety Stress Scales (DASS-21), completed by survivor in reference to past week. Range: 0 to 21; higher scores indicate greater anxiety.'}, {'measure': 'Change in Supporter Anxiety at 3 Months Post-baseline (Self Report)', 'timeFrame': 'Baseline, 3 months', 'description': 'Sum score on the Anxiety subscale of the Depression and Anxiety Stress Scales (DASS-21), completed by supporter in reference to past week. Range: 0 to 21; higher scores indicate greater anxiety.'}, {'measure': 'Change in Survivor Role Impairment at 3 Months Post-baseline (Self Report)', 'timeFrame': 'Baseline, 3 months', 'description': 'Sum score on Work/School/Responsibility Impairment subscale of the Behavioral Activation for Depression Scale (BADS), completed by survivor in reference to past week. Range: 0 to 30; higher scores indicate more impairment.'}, {'measure': 'Change in Survivor Social Impairment at 3 Months Post-baseline (Self Report)', 'timeFrame': 'Baseline, 3 months', 'description': 'Sum score on Social Impairment subscale of the Behavioral Activation for Depression Scale (BADS), completed by survivor in reference to past week. Range: 0 to 30; higher scores indicate more impairment.'}, {'measure': 'Change in Survivor Flourishing at 3 Months Post-baseline (Self Report)', 'timeFrame': 'Baseline, 3 months', 'description': 'Sum score on Flourishing Index Measure, completed by survivor. Range: 0 to 120; higher scores indicate more flourishing.'}, {'measure': 'Change in Supporter Flourishing at 3 Months Post-baseline (Self Report)', 'timeFrame': 'Baseline, 3 months', 'description': 'Sum score on Flourishing Index Measure, completed by supporter. Range: 0 to 120; higher scores indicate more flourishing.'}, {'measure': 'Survivor Distress Associated With Supporter Negative Reactions at 1 Month Post-baseline (Self Report)', 'timeFrame': '1 month', 'description': "Mean score on ratings of distress associated endorsed items on Negative Reactions subscale of the Social Reactions Questionnaire - Shortened, completed by survivor in reference to supporter's reactions to survivor in past month. Range: 0 to 3; higher scores indicate more distress."}, {'measure': 'Supporter Positive Reactions to Disclosure at 1 Month Post-baseline (Informant Report)', 'timeFrame': '1 month', 'description': "Sum score on Positive Reactions subscale of the Social Reactions Questionnaire - Shortened, completed by survivor in reference to supporter's reactions in past month. Range: 0 to 16; higher scores indicate more frequent positive reactions."}, {'measure': 'Change in Survivor Typical Alcohol Consumption (Quantity) at 3 Months Post-baseline (Self Report)', 'timeFrame': 'Baseline, 3 months', 'description': 'Number of typical drinks per week in past month reported by survivor on the Daily Drinking Questionnaire'}, {'measure': 'Change in Survivor Typical Alcohol Consumption (Frequency) at 3 Months Post-baseline (Self Report)', 'timeFrame': 'Baseline, 3 months', 'description': 'Number of typical drinking days per week in past month reported by survivor on the Daily Drinking Questionnaire. Range: 0 to 7.'}, {'measure': 'Change in Survivor Typical Alcohol Consumption (Hours) at 3 Months Post-baseline (Self Report)', 'timeFrame': 'Baseline, 3 months', 'description': 'Number of typical drinking hours per week in past month reported by survivor on the Daily Drinking Questionnaire.'}, {'measure': 'Supporter Perceived Helping Ineffectiveness at 1 Month Post-baseline (Self Report)', 'timeFrame': '1 month', 'description': 'Sum score on the Confusion subscale of the Impact on Friends measure, completed by supporter in reference to the past month. Range: 6 to 30; higher scores indicate greater perceived ineffectiveness.'}, {'measure': 'Supporter Distress in Helping at 1 Month Post-baseline (Self Report)', 'timeFrame': '1 month', 'description': 'Sum score on the Emotional Distress subscale of the Impact on Friends measure, completed by supporter in reference to the past month. Range: 24 to 120; higher scores indicate greater distress.'}, {'measure': 'Supporter Accommodation of Survivor PTSD Symptoms at 1 Month Post-baseline (Self Report)', 'timeFrame': '1 month', 'description': "Sum score on the Significant Others' Responses to Trauma Scale (SORTS), completed by supporter in reference to the past month. Range: 0 to 112; higher scores indicate greater accommodation."}, {'measure': 'Change in Survivor Cannabis Use Frequency at 3 Months Post-baseline (Self Report)', 'timeFrame': 'Baseline, 3 months', 'description': 'Number of days of cannabis use in past 2 weeks, as reported by survivor. Range: 0 to 14.'}, {'measure': 'Change in Survivor Prescription Opioid Misuse Frequency at 3 Months Post-baseline (Self Report)', 'timeFrame': 'Baseline, 3 months', 'description': 'Number of days of prescription opioid use not as prescribed in past 2 weeks, as reported by survivor. Range: 0 to 14.'}, {'measure': 'Change in Survivor Non-prescription Opioid Use Frequency at 3 Months Post-baseline (Self Report)', 'timeFrame': 'Baseline, 3 months', 'description': 'Number of days of non-prescription opioid use in past 2 weeks, as reported by survivor. Range: 0 to 14.'}, {'measure': 'Change in Survivor Prescription Amphetamine Misuse Frequency at 3 Months Post-baseline (Self Report)', 'timeFrame': 'Baseline, 3 months', 'description': 'Number of days of prescription amphetamine use not as prescribed in past 2 weeks, as reported by survivor. Range: 0 to 14.'}, {'measure': 'Change in Survivor Methamphetamine Use Frequency at 3 Months Post-baseline (Self Report)', 'timeFrame': 'Baseline, 3 months', 'description': 'Number of days of methamphetamine use in past 2 weeks, as reported by survivor. Range: 0 to 14.'}, {'measure': 'Change in Survivor Cigarette Use Frequency at 3 Months Post-baseline (Self Report)', 'timeFrame': 'Baseline, 3 months', 'description': 'Number of days of cigarette use in past 2 weeks, as reported by survivor. Range: 0 to 14.'}, {'measure': 'Change in Survivor Cigarette Use Quantity at 3 Months Post-baseline (Self Report)', 'timeFrame': 'Baseline, 3 months', 'description': 'Number of cigarettes smoked in a typical day in past 2 weeks, as reported by survivor.'}]}, 'oversightModule': {'oversightHasDmc': False, 'isFdaRegulatedDrug': False, 'isFdaRegulatedDevice': False}, 'conditionsModule': {'conditions': ['Stress Disorders, Post-Traumatic', 'Helping Behavior', 'Help-Seeking Behavior', 'Stress', 'Relationship, Social', 'Sexual Assault', 'Sexual Violence', 'Social Interaction']}, 'referencesModule': {'references': [{'pmid': '35817294', 'type': 'DERIVED', 'citation': 'Dworkin ER, Ruzek JI, Cordova MJ, Fitzpatrick S, Merchant L, Stewart T, Santos JP, Mohr J, Bedard-Gilligan M. Supporter-focused early intervention for recent sexual assault survivors: Study protocol for a pilot randomized clinical trial. Contemp Clin Trials. 2022 Aug;119:106848. doi: 10.1016/j.cct.2022.106848. Epub 2022 Jul 9.'}]}, 'descriptionModule': {'briefSummary': "Communication and Recovery Enhancement (CARE) is a 2-session early intervention for survivors of recent sexual assault and their supporters that aims to improve supporters' ability to respond effectively. The goal of this pilot trial is to understand the acceptability and preliminary efficacy of two versions of CARE: a version in which survivors and supporters attend both sessions together (dyadic CARE) and a version in which supporters attend sessions alone (supporter-only CARE). Survivors aged 14+ with elevated posttraumatic stress symptoms will enroll with a supporter of their choosing. Dyads will be randomized to dyadic CARE, supporter-only CARE, or waitlist control, and will complete self-report assessments at baseline, post-session-1, and follow-ups (1, 2, and 3 months post-baseline). Results will be used to inform future changes to CARE and determine whether a fully-powered randomized controlled trial is warranted."}, 'eligibilityModule': {'sex': 'ALL', 'stdAges': ['CHILD', 'ADULT', 'OLDER_ADULT'], 'minimumAge': '14 Years', 'healthyVolunteers': False, 'eligibilityCriteria': "Inclusion Criteria (Survivors):\n\n* Age 14+ years\n* Can speak/read English or Spanish\n* Have access to a Zoom-capable device\n* Screened for eligibility within 10 weeks of sexual assault, defined as any unwanted, distressing sexual contact (e.g., unwanted touching, coerced sexual activity, rape)\n* Able to attend first study session within 2 weeks of screening\n* Elevated PTSD symptoms at screening as operationalized by a Primary Care PTSD Screen score of 2/5 or above\n* Able to identify an eligible supporter\n* Have a way to receive survey links and complete surveys privately (i.e., without potential device or account access by the supporter)\n\nInclusion Criteria (Supporters):\n\n* Age 14+ years\n* Can speak/read English or Spanish\n* Have access to a Zoom-capable device\n* Able to attend first study session within 2 weeks of survivor's screening\n* Are in contact with the survivor at least once a week\n* In the opinion of the survivor, are able to make an independent decision about whether or not to participate in the study\n* Have a way to receive survey links and complete surveys privately (i.e., without potential device or account access by the survivor)\n\nExclusion Criteria (Survivors):\n\n* Active psychosis\n* Active suicidal intent\n\nExclusion Criteria (Supporters):\n\n* Perpetrated the sexual assault\n* Engaged in severe past-year violence or abuse (as defined by the survivor) against the survivor\n* The survivor has not told the supporter about the sexual assault at the time of screening and was not already planning to tell the supporter\n* In the opinion of the survivor, relational conflict exists between the survivor and supporter that potentially could be exacerbated by program participation"}, 'identificationModule': {'nctId': 'NCT05345405', 'acronym': 'CARE', 'briefTitle': 'Clinical Trial of a Supporter-Targeted Intervention to Improve Outcomes in Recent Sexual Assault Survivors', 'organization': {'class': 'OTHER', 'fullName': 'University of Washington'}, 'officialTitle': 'Improving Social Support Quality Among Survivors Seeking Acute Post-Rape Care: Testing a Supporter-Targeted Intervention', 'orgStudyIdInfo': {'id': 'STUDY00011982'}}, 'armsInterventionsModule': {'armGroups': [{'type': 'ACTIVE_COMPARATOR', 'label': 'Dyadic CARE', 'description': 'Participants will receive dyadic CARE following baseline and will complete self-report assessments at post-session-1, Month 1, Month 2, and Month 3.', 'interventionNames': ['Behavioral: Dyadic CARE']}, {'type': 'ACTIVE_COMPARATOR', 'label': 'Supporter-Only CARE', 'description': 'Participants will receive supporter-only CARE following baseline and will complete self-report assessments at post-session-1, Month 1, Month 2, and Month 3.', 'interventionNames': ['Behavioral: Supporter-Only CARE']}, {'type': 'NO_INTERVENTION', 'label': 'Waitlist Control', 'description': 'After completing baseline, participants will be invited to schedule a CARE session in 3 months (i.e., after the completion of all study assessments). The version of CARE received at that point will be selected by the survivor. Participants will complete self-report assessments at post-session-1, Month 1, Month 2, and Month 3.'}], 'interventions': [{'name': 'Dyadic CARE', 'type': 'BEHAVIORAL', 'description': "Dyadic CARE involves two telehealth sessions with a clinician, the survivor, and a supporter of the survivor's choice. Session content uses cognitive-behavioral strategies (e.g., encouraging non-avoidance) to encourage communication and improve supporters' responses in trauma-related conversations. Between sessions, both the survivor and the supporter are instructed to review session content and have guided discussions with the assistance of a workbook.", 'armGroupLabels': ['Dyadic CARE']}, {'name': 'Supporter-Only CARE', 'type': 'BEHAVIORAL', 'description': "Supporter-only CARE involves two telehealth sessions with a clinician and a supporter of the survivor's choice, without the survivor present. Session content uses cognitive-behavioral strategies (e.g., encouraging non-avoidance) to encourage communication and improve supporters' responses in trauma-related conversations. Between sessions, both the survivor and the supporter are instructed to review session content and have guided discussions with the assistance of a workbook.", 'armGroupLabels': ['Supporter-Only CARE']}]}, 'contactsLocationsModule': {'locations': [{'zip': '98195-7238', 'city': 'Seattle', 'state': 'Washington', 'country': 'United States', 'facility': 'University of Washington School of Medicine', 'geoPoint': {'lat': 47.60621, 'lon': -122.33207}}], 'overallOfficials': [{'name': 'Emily R Dworkin, PhD', 'role': 'PRINCIPAL_INVESTIGATOR', 'affiliation': 'University of Washington'}]}, 'ipdSharingStatementModule': {'infoTypes': ['STUDY_PROTOCOL', 'ICF', 'ANALYTIC_CODE'], 'ipdSharing': 'YES', 'description': 'Data will be archived in the National Archive of Criminal Justice Data. No direct or indirect identifiers will ever be included in the archived dataset. We will submit study instruments and data collection forms, project reports describing our methods, and Institutional Review Board documentation (including copies of consent forms). A syntax file will include (1) recoding of reverse-scored items; (2) calculation of scale scores; (3) addition of a filter variable indicating any cases not included in any final analyses and the corresponding reason for exclusion; and (5) variable and value labels. Technical documentation for the dataset will include variable codebooks with full study instruments and citations, naming conventions, missing value designations, value labels, known data anomalies, and a data user guide.'}, 'sponsorCollaboratorsModule': {'leadSponsor': {'name': 'University of Washington', 'class': 'OTHER'}, 'responsibleParty': {'type': 'PRINCIPAL_INVESTIGATOR', 'investigatorTitle': 'Assistant Professor, School of Medicine: Psychiatry', 'investigatorFullName': 'Emily Dworkin', 'investigatorAffiliation': 'University of Washington'}}}}