Ignite Creation Date:
2025-12-25 @ 12:45 AM
Ignite Modification Date:
2026-02-09 @ 6:12 AM
Study NCT ID:
NCT02355067
Status:
COMPLETED
Last Update Posted:
2021-03-09
First Post:
2015-01-30
Is NOT Gene Therapy:
True
Has Adverse Events:
True
Brief Title:
Social Media Intervention for Postpartum Depression
Sponsor:
Organization:
Raw JSON
{'hasResults': True, 'derivedSection': {'miscInfoModule': {'versionHolder': '2025-12-24'}, 'conditionBrowseModule': {'meshes': [{'id': 'D019052', 'term': 'Depression, Postpartum'}, {'id': 'D003863', 'term': 'Depression'}], 'ancestors': [{'id': 'D011644', 'term': 'Puerperal Disorders'}, {'id': 'D011248', 'term': 'Pregnancy Complications'}, {'id': 'D005261', 'term': 'Female Urogenital Diseases and Pregnancy Complications'}, {'id': 'D000091642', 'term': 'Urogenital Diseases'}, {'id': 'D003866', 'term': 'Depressive Disorder'}, {'id': 'D019964', 'term': 'Mood Disorders'}, {'id': 'D001523', 'term': 'Mental Disorders'}, {'id': 'D001526', 'term': 'Behavioral Symptoms'}, {'id': 'D001519', 'term': 'Behavior'}]}}, 'resultsSection': {'moreInfoModule': {'pointOfContact': {'email': 'guevara@email.chop.edu', 'phone': '215-590-1130', 'title': 'Dr. James Guevara', 'organization': "Children's Hospital of Philadelphia"}, 'certainAgreement': {'piSponsorEmployee': False, 'restrictiveAgreement': False}}, 'adverseEventsModule': {'timeFrame': '3 months from enrollment to second study visit', 'eventGroups': [{'id': 'EG000', 'title': 'Social Media Format', 'description': 'Social Media Intervention for women with postpartum depression (PPD) symptoms\n\nSocial Media Intervention: These women will participate in the intervention through the online Facebook group.', 'otherNumAtRisk': 12, 'deathsNumAtRisk': 12, 'otherNumAffected': 0, 'seriousNumAtRisk': 12, 'deathsNumAffected': 0, 'seriousNumAffected': 0}, {'id': 'EG001', 'title': 'In-Person Format', 'description': 'Traditional In-Person Intervention for Women with postpartum depression (PPD)\n\nTraditional In-Person Intervention: These women will participate in the intervention through a traditional weekly meeting of a group in-person.', 'otherNumAtRisk': 12, 'deathsNumAtRisk': 12, 'otherNumAffected': 0, 'seriousNumAtRisk': 12, 'deathsNumAffected': 0, 'seriousNumAffected': 0}], 'frequencyThreshold': '0'}, 'outcomeMeasuresModule': {'outcomeMeasures': [{'type': 'PRIMARY', 'title': 'Attendance', 'denoms': [{'units': 'Participants', 'counts': [{'value': '12', 'groupId': 'OG000'}, {'value': '12', 'groupId': 'OG001'}]}], 'groups': [{'id': 'OG000', 'title': 'Social Media Format', 'description': 'Social Media Intervention for women with postpartum depression (PPD) symptoms\n\nSocial Media Intervention: These women will participate in the intervention through the online Facebook group.'}, {'id': 'OG001', 'title': 'In-Person Format', 'description': 'Traditional In-Person Intervention for Women with postpartum depression (PPD)\n\nTraditional In-Person Intervention: These women will participate in the intervention through a traditional weekly meeting of a group in-person.'}], 'classes': [{'categories': [{'measurements': [{'value': '83.3', 'groupId': 'OG000', 'lowerLimit': '67', 'upperLimit': '100'}, {'value': '3.3', 'groupId': 'OG001', 'lowerLimit': '0', 'upperLimit': '33'}]}]}], 'paramType': 'MEAN', 'timeFrame': '8 weeks', 'description': 'Percentage of participants who attend each group session or check in online weekly. This is averaged over the course of the 8-week program.', 'unitOfMeasure': 'percentage of participants', 'dispersionType': 'Full Range', 'reportingStatus': 'POSTED'}, {'type': 'PRIMARY', 'title': 'Acceptability', 'denoms': [{'units': 'Participants', 'counts': [{'value': '9', 'groupId': 'OG000'}, {'value': '4', 'groupId': 'OG001'}]}], 'groups': [{'id': 'OG000', 'title': 'Social Media Format', 'description': 'Social Media Intervention for women with postpartum depression (PPD) symptoms\n\nSocial Media Intervention: These women will participate in the intervention through the online Facebook group.'}, {'id': 'OG001', 'title': 'In-Person Format', 'description': 'Traditional In-Person Intervention for Women with postpartum depression (PPD)\n\nTraditional In-Person Intervention: These women will participate in the intervention through a traditional weekly meeting of a group in-person.'}], 'classes': [{'categories': [{'measurements': [{'value': '4.5', 'groupId': 'OG000', 'lowerLimit': '1', 'upperLimit': '5'}, {'value': '4.5', 'groupId': 'OG001', 'lowerLimit': '1', 'upperLimit': '5'}]}]}], 'paramType': 'MEAN', 'timeFrame': '12 weeks', 'description': 'Participants report concerning their overall program effects-Satisfaction Questionnaire. The scale ranges from 1-5 with higher values representing higher satisfaction.', 'unitOfMeasure': 'units on a scale', 'dispersionType': 'Full Range', 'reportingStatus': 'POSTED'}, {'type': 'SECONDARY', 'title': 'Beck Depression Inventory (BDI-II)', 'denoms': [{'units': 'Participants', 'counts': [{'value': '12', 'groupId': 'OG000'}, {'value': '8', 'groupId': 'OG001'}]}], 'groups': [{'id': 'OG000', 'title': 'Social Media Format', 'description': 'Social Media Intervention for women with postpartum depression (PPD) symptoms\n\nSocial Media Intervention: These women will participate in the intervention through the online Facebook group.'}, {'id': 'OG001', 'title': 'In-Person Format', 'description': 'Traditional In-Person Intervention for Women with postpartum depression (PPD)\n\nTraditional In-Person Intervention: These women will participate in the intervention through a traditional weekly meeting of a group in-person.'}], 'classes': [{'categories': [{'measurements': [{'value': '20.2', 'groupId': 'OG000', 'lowerLimit': '17', 'upperLimit': '40'}, {'value': '23.3', 'groupId': 'OG001', 'lowerLimit': '14', 'upperLimit': '33'}]}]}], 'paramType': 'MEAN', 'timeFrame': '12 weeks', 'description': 'The BDI-II is a 21-item self-report tool that measures the severity of depression and includes two subscales: cognitive and somatic. It has been well validated, with scores 14-19 indicating mild depression, 20-28 moderate depression, and 29-63 severe depression. The full range of the BDI-II is 0-64.', 'unitOfMeasure': 'units on a scale', 'dispersionType': 'Full Range', 'reportingStatus': 'POSTED'}, {'type': 'SECONDARY', 'title': 'Parenting Sense of Competency (PSOC) Scale', 'denoms': [{'units': 'Participants', 'counts': [{'value': '12', 'groupId': 'OG000'}, {'value': '8', 'groupId': 'OG001'}]}], 'groups': [{'id': 'OG000', 'title': 'Social Media Format', 'description': 'Social Media Intervention for women with postpartum depression (PPD) symptoms\n\nSocial Media Intervention: These women will participate in the intervention through the online Facebook group.'}, {'id': 'OG001', 'title': 'In-Person Format', 'description': 'Traditional In-Person Intervention for Women with postpartum depression (PPD)\n\nTraditional In-Person Intervention: These women will participate in the intervention through a traditional weekly meeting of a group in-person.'}], 'classes': [{'categories': [{'measurements': [{'value': '76.3', 'groupId': 'OG000', 'lowerLimit': '54', 'upperLimit': '97'}, {'value': '73.6', 'groupId': 'OG001', 'lowerLimit': '60', 'upperLimit': '92'}]}]}], 'paramType': 'MEAN', 'timeFrame': '12 weeks', 'description': "The Parenting Sense of Competence scale measures parental competence on two dimensions: Satisfaction and Efficacy. It is a 17 item Likert-scale questionnaire (on a 6 point scale ranging from strongly agree \\[1\\] to strongly disagree \\[6\\]), with nine questions under Satisfaction and seven under Efficacy. Satisfaction section examines the parents' anxiety, motivation and frustration, while the Efficacy section looks at the parents' competence, capability levels, and problem-solving abilities in their parental role. Higher scores represent better parenting sense of competency. The full range of the score is 17-102.", 'unitOfMeasure': 'units on a scale', 'dispersionType': 'Full Range', 'reportingStatus': 'POSTED'}]}, 'participantFlowModule': {'groups': [{'id': 'FG000', 'title': 'Social Media Format', 'description': 'Social Media Intervention for women with postpartum depression (PPD) symptoms\n\nSocial Media Intervention: These women will participate in the intervention through the online Facebook group.'}, {'id': 'FG001', 'title': 'In-Person Format', 'description': 'Traditional In-Person Intervention for Women with postpartum depression (PPD)\n\nTraditional In-Person Intervention: These women will participate in the intervention through a traditional weekly meeting of a group in-person.'}], 'periods': [{'title': 'Overall Study', 'milestones': [{'type': 'STARTED', 'achievements': [{'groupId': 'FG000', 'numSubjects': '20'}, {'groupId': 'FG001', 'numSubjects': '20'}]}, {'type': 'COMPLETED', 'achievements': [{'groupId': 'FG000', 'numSubjects': '12'}, {'groupId': 'FG001', 'numSubjects': '12'}]}, {'type': 'NOT COMPLETED', 'achievements': [{'groupId': 'FG000', 'numSubjects': '8'}, {'groupId': 'FG001', 'numSubjects': '8'}]}]}]}, 'baselineCharacteristicsModule': {'denoms': [{'units': 'Participants', 'counts': [{'value': '12', 'groupId': 'BG000'}, {'value': '12', 'groupId': 'BG001'}, {'value': '24', 'groupId': 'BG002'}]}], 'groups': [{'id': 'BG000', 'title': 'Social Media Format', 'description': 'Social Media Intervention for women with postpartum depression (PPD) symptoms\n\nSocial Media Intervention: These women will participate in the intervention through the online Facebook group.'}, {'id': 'BG001', 'title': 'In-Person Format', 'description': 'Traditional In-Person Intervention for Women with postpartum depression (PPD)\n\nTraditional In-Person Intervention: These women will participate in the intervention through a traditional weekly meeting of a group in-person.'}, {'id': 'BG002', 'title': 'Total', 'description': 'Total of all reporting groups'}], 'measures': [{'title': 'Age, Categorical', 'classes': [{'categories': [{'title': '<=18 years', 'measurements': [{'value': '1', 'groupId': 'BG000'}, {'value': '1', 'groupId': 'BG001'}, {'value': '2', 'groupId': 'BG002'}]}, {'title': 'Between 18 and 65 years', 'measurements': [{'value': '11', 'groupId': 'BG000'}, {'value': '11', 'groupId': 'BG001'}, {'value': '22', 'groupId': 'BG002'}]}, {'title': '>=65 years', 'measurements': [{'value': '0', 'groupId': 'BG000'}, {'value': '0', 'groupId': 'BG001'}, {'value': '0', 'groupId': 'BG002'}]}]}], 'paramType': 'COUNT_OF_PARTICIPANTS', 'unitOfMeasure': 'Participants'}, {'title': 'Age, Continuous', 'classes': [{'categories': [{'measurements': [{'value': '26.4', 'spread': '1.9', 'groupId': 'BG000'}, {'value': '26.3', 'spread': '1.8', 'groupId': 'BG001'}, {'value': '26.3', 'spread': '1.9', 'groupId': 'BG002'}]}]}], 'paramType': 'MEAN', 'unitOfMeasure': 'years', 'dispersionType': 'STANDARD_DEVIATION'}, {'title': 'Sex: Female, Male', 'classes': [{'categories': [{'title': 'Female', 'measurements': [{'value': '12', 'groupId': 'BG000'}, {'value': '12', 'groupId': 'BG001'}, {'value': '24', 'groupId': 'BG002'}]}, {'title': 'Male', 'measurements': [{'value': '0', 'groupId': 'BG000'}, {'value': '0', 'groupId': 'BG001'}, {'value': '0', 'groupId': 'BG002'}]}]}], 'paramType': 'COUNT_OF_PARTICIPANTS', 'unitOfMeasure': 'Participants'}, {'title': 'Race (NIH/OMB)', 'classes': [{'categories': [{'title': 'American Indian or Alaska Native', 'measurements': [{'value': '0', 'groupId': 'BG000'}, {'value': '0', 'groupId': 'BG001'}, {'value': '0', 'groupId': 'BG002'}]}, {'title': 'Asian', 'measurements': [{'value': '0', 'groupId': 'BG000'}, {'value': '0', 'groupId': 'BG001'}, {'value': '0', 'groupId': 'BG002'}]}, {'title': 'Native Hawaiian or Other Pacific Islander', 'measurements': [{'value': '0', 'groupId': 'BG000'}, {'value': '0', 'groupId': 'BG001'}, {'value': '0', 'groupId': 'BG002'}]}, {'title': 'Black or African American', 'measurements': [{'value': '9', 'groupId': 'BG000'}, {'value': '11', 'groupId': 'BG001'}, {'value': '20', 'groupId': 'BG002'}]}, {'title': 'White', 'measurements': [{'value': '0', 'groupId': 'BG000'}, {'value': '1', 'groupId': 'BG001'}, {'value': '1', 'groupId': 'BG002'}]}, {'title': 'More than one race', 'measurements': [{'value': '3', 'groupId': 'BG000'}, {'value': '0', 'groupId': 'BG001'}, {'value': '3', 'groupId': 'BG002'}]}, {'title': 'Unknown or Not Reported', 'measurements': [{'value': '0', 'groupId': 'BG000'}, {'value': '0', 'groupId': 'BG001'}, {'value': '0', 'groupId': 'BG002'}]}]}], 'paramType': 'COUNT_OF_PARTICIPANTS', 'unitOfMeasure': 'Participants'}, {'title': 'Region of Enrollment', 'classes': [{'title': 'United States', 'categories': [{'measurements': [{'value': '12', 'groupId': 'BG000'}, {'value': '12', 'groupId': 'BG001'}, {'value': '24', 'groupId': 'BG002'}]}]}], 'paramType': 'COUNT_OF_PARTICIPANTS', 'unitOfMeasure': 'Participants'}, {'title': 'Beck Depression Inventory II', 'classes': [{'categories': [{'measurements': [{'value': '30.7', 'groupId': 'BG000', 'lowerLimit': '17', 'upperLimit': '46'}, {'value': '25.7', 'groupId': 'BG001', 'lowerLimit': '18', 'upperLimit': '35'}, {'value': '28.2', 'groupId': 'BG002', 'lowerLimit': '17', 'upperLimit': '46'}]}]}], 'paramType': 'MEAN', 'description': 'The BDI-II is a 21-item self-report tool that measures the severity of depression and includes two subscales: cognitive and somatic. It has been well validated, with scores 14-19 indicating mild depression, 20-28 moderate depression, and 29-63 severe depression. The full range of the BDI-II is 0-64.', 'unitOfMeasure': 'units on a scale', 'dispersionType': 'FULL_RANGE'}, {'title': 'Parenting Sense of Competency', 'classes': [{'categories': [{'measurements': [{'value': '67.8', 'groupId': 'BG000', 'lowerLimit': '54', 'upperLimit': '83'}, {'value': '78.3', 'groupId': 'BG001', 'lowerLimit': '63', 'upperLimit': '97'}, {'value': '73.0', 'groupId': 'BG002', 'lowerLimit': '54', 'upperLimit': '97'}]}]}], 'paramType': 'MEAN', 'description': 'Measures parental competence on 2 dimensions: Satisfaction and Efficacy. 17-item Likert-scale questionnaire (on a 6 point scale ranging from strongly agree \\[1\\] to strongly disagree \\[6\\]). Higher scores represent better parenting sense of competency. The full range of the score is 17-102.', 'unitOfMeasure': 'units on a scale', 'dispersionType': 'FULL_RANGE'}]}}, 'documentSection': {'largeDocumentModule': {'largeDocs': [{'date': '2015-09-08', 'size': 415443, 'label': 'Informed Consent Form', 'hasIcf': True, 'hasSap': False, 'filename': 'ICF_000.pdf', 'typeAbbrev': 'ICF', 'uploadDate': '2017-10-23T11:04', 'hasProtocol': False}, {'date': '2015-09-11', 'size': 935004, 'label': 'Study Protocol and Statistical Analysis Plan', 'hasIcf': False, 'hasSap': True, 'filename': 'Prot_SAP_001.pdf', 'typeAbbrev': 'Prot_SAP', 'uploadDate': '2017-10-23T11:12', 'hasProtocol': True}]}}, 'protocolSection': {'designModule': {'phases': ['NA'], 'studyType': 'INTERVENTIONAL', 'designInfo': {'allocation': 'RANDOMIZED', 'maskingInfo': {'masking': 'NONE'}, 'primaryPurpose': 'SUPPORTIVE_CARE', 'interventionModel': 'PARALLEL'}, 'enrollmentInfo': {'type': 'ACTUAL', 'count': 40}}, 'statusModule': {'overallStatus': 'COMPLETED', 'startDateStruct': {'date': '2015-01'}, 'expandedAccessInfo': {'hasExpandedAccess': False}, 'statusVerifiedDate': '2021-02', 'completionDateStruct': {'date': '2017-11-03', 'type': 'ACTUAL'}, 'lastUpdateSubmitDate': '2021-02-18', 'studyFirstSubmitDate': '2015-01-30', 'resultsFirstSubmitDate': '2017-11-01', 'studyFirstSubmitQcDate': '2015-02-03', 'lastUpdatePostDateStruct': {'date': '2021-03-09', 'type': 'ACTUAL'}, 'resultsFirstSubmitQcDate': '2019-09-05', 'studyFirstPostDateStruct': {'date': '2015-02-04', 'type': 'ESTIMATED'}, 'resultsFirstPostDateStruct': {'date': '2019-10-02', 'type': 'ACTUAL'}, 'primaryCompletionDateStruct': {'date': '2017-11-03', 'type': 'ACTUAL'}}, 'outcomesModule': {'primaryOutcomes': [{'measure': 'Attendance', 'timeFrame': '8 weeks', 'description': 'Percentage of participants who attend each group session or check in online weekly. This is averaged over the course of the 8-week program.'}, {'measure': 'Acceptability', 'timeFrame': '12 weeks', 'description': 'Participants report concerning their overall program effects-Satisfaction Questionnaire. The scale ranges from 1-5 with higher values representing higher satisfaction.'}], 'secondaryOutcomes': [{'measure': 'Beck Depression Inventory (BDI-II)', 'timeFrame': '12 weeks', 'description': 'The BDI-II is a 21-item self-report tool that measures the severity of depression and includes two subscales: cognitive and somatic. It has been well validated, with scores 14-19 indicating mild depression, 20-28 moderate depression, and 29-63 severe depression. The full range of the BDI-II is 0-64.'}, {'measure': 'Parenting Sense of Competency (PSOC) Scale', 'timeFrame': '12 weeks', 'description': "The Parenting Sense of Competence scale measures parental competence on two dimensions: Satisfaction and Efficacy. It is a 17 item Likert-scale questionnaire (on a 6 point scale ranging from strongly agree \\[1\\] to strongly disagree \\[6\\]), with nine questions under Satisfaction and seven under Efficacy. Satisfaction section examines the parents' anxiety, motivation and frustration, while the Efficacy section looks at the parents' competence, capability levels, and problem-solving abilities in their parental role. Higher scores represent better parenting sense of competency. The full range of the score is 17-102."}]}, 'oversightModule': {'oversightHasDmc': False, 'isFdaRegulatedDrug': False, 'isFdaRegulatedDevice': False}, 'conditionsModule': {'keywords': ['parenting', 'postpartum depression', 'mothers', 'infants', 'depression'], 'conditions': ['Postpartum Depression', 'Parenting']}, 'descriptionModule': {'briefSummary': 'This study is intended to compare the acceptability and feasibility and explore outcomes related to two different formats of a parenting program for mothers with postpartum depressive symptoms. One version will be a traditional, in-person group format, while the other will be a social media group format. The investigators will also explore the differences in outcomes of both formats, looking at depressive symptoms, parenting sense of competency, and parenting interactions with children.', 'detailedDescription': 'Postpartum depressive symptoms are common among women following the birth of a child and can adversely impact a mother\'s ability to care for her child. Evidence-based parent coaching programs have been developed to guide mothers with caring for their infants but do not address the effects of depression on parenting, can be expensive to administer, and are not available in a format that facilitates participation by women with depressive symptoms. We have adapted a previously validated parent coaching intervention, the Parents Interacting with Infants (PIWI) program, for use with depressed parents by inclusion of educational material based on Beardslee\'s cognitive psycho-educational family model. The program spans 8 weeks, each week focusing on a specific topic. The topics covered are: psychoeducation regarding depression and behavioral activation for coping with high levels of stress, sleep, play, laughter, feeding, temperament, safety, and reading with infants.\n\nWe will conduct a pilot randomized controlled trial comparing two versions of the parent coaching program: social media and traditional in-person group formats. We\'ve modified the PIWI program to address barriers to participation through social media format using secret Facebook user groups. We will assess the feasibility and acceptability of the social media program compared to a traditional group format by examining the proportion of subjects who attend group sessions or "like" Facebook sessions. Women who consent to participate in the study will be assigned by randomization to one format or the other in blocks of 20.\n\nWomen will complete measures of feasibility and acceptability and measures of depressive symptoms, Beck Depression Inventory-II (BDI-II - Appendix 2) Scale and parenting competence, Parenting Sense of Competency (PSOC - Appendix 3 scales) prior to (time 0) and after the intervention (time 8-12 weeks post enrollment). In addition, mothers and infants in phase III will be videotaped during a 16-minute free play using a standardized measure of parenting interaction (PICCOLO) following completion of the intervention. The measures will provide important information on the effects of parent coaching formats on a new mother\'s depressive symptoms, her sense of parenting confidence, and her parenting interactions with her infant.'}, 'eligibilityModule': {'sex': 'FEMALE', 'stdAges': ['CHILD', 'ADULT', 'OLDER_ADULT'], 'minimumAge': '15 Years', 'healthyVolunteers': True, 'eligibilityCriteria': 'Inclusion Criteria:\n\n1. Females\n2. 15 years of age or older at the start of the study\n3. English speaking\n4. Access to the internet via a computer or a smartphone\n5. Mother of a child 1-3 months old\n6. Edinburgh Postnatal Depression Scale (EPDS) score of 9 or higher\n7. Informed consent and HIPAA authorization.\n\nExclusion Criteria:\n\n1\\) Have significant suicidal symptoms. Significant suicide risk is defined as current suicidal intent and a plan for suicidal behavior.'}, 'identificationModule': {'nctId': 'NCT02355067', 'briefTitle': 'Social Media Intervention for Postpartum Depression', 'organization': {'class': 'OTHER', 'fullName': "Children's Hospital of Philadelphia"}, 'officialTitle': 'Social Media Intervention to Teach Parenting for Women With Postpartum Depression', 'orgStudyIdInfo': {'id': '14-011491'}}, 'armsInterventionsModule': {'armGroups': [{'type': 'EXPERIMENTAL', 'label': 'Social Media Format', 'description': 'Social Media Intervention for women with postpartum depression (PPD) symptoms', 'interventionNames': ['Behavioral: Social Media Intervention']}, {'type': 'ACTIVE_COMPARATOR', 'label': 'In-Person Format', 'description': 'Traditional In-Person Intervention for Women with postpartum depression (PPD)', 'interventionNames': ['Behavioral: Traditional In-Person Intervention']}], 'interventions': [{'name': 'Social Media Intervention', 'type': 'BEHAVIORAL', 'description': 'These women will participate in the intervention through the online Facebook group.', 'armGroupLabels': ['Social Media Format']}, {'name': 'Traditional In-Person Intervention', 'type': 'BEHAVIORAL', 'description': 'These women will participate in the intervention through a traditional weekly meeting of a group in-person.', 'armGroupLabels': ['In-Person Format']}]}, 'contactsLocationsModule': {'locations': [{'zip': '19104', 'city': 'Philadelphia', 'state': 'Pennsylvania', 'country': 'United States', 'facility': "The Children's Hospital of Philadelphia", 'geoPoint': {'lat': 39.95238, 'lon': -75.16362}}], 'overallOfficials': [{'name': 'James P Guevara, MD, MPH', 'role': 'PRINCIPAL_INVESTIGATOR', 'affiliation': "Children's Hospital of Philadelphia"}]}, 'sponsorCollaboratorsModule': {'leadSponsor': {'name': "Children's Hospital of Philadelphia", 'class': 'OTHER'}, 'collaborators': [{'name': 'The Oscar G. & Elsa S. Mayer Family Foundation', 'class': 'UNKNOWN'}, {'name': 'University of Pennsylvania', 'class': 'OTHER'}], 'responsibleParty': {'type': 'SPONSOR'}}}}