Ignite Creation Date:
2025-12-25 @ 4:31 AM
Ignite Modification Date:
2026-02-20 @ 8:16 AM
Study NCT ID:
NCT01593618
Status:
COMPLETED
Last Update Posted:
2017-12-02
First Post:
2012-05-04
Is Gene Therapy:
True
Has Adverse Events:
False
Brief Title:
Empowering Cancer Survivors Through Information Technology
Sponsor:
Organization:
Raw JSON
{'hasResults': False, 'derivedSection': {'miscInfoModule': {'versionHolder': '2025-12-24'}, 'interventionBrowseModule': {'meshes': [{'id': 'D059039', 'term': 'Standard of Care'}], 'ancestors': [{'id': 'D019984', 'term': 'Quality Indicators, Health Care'}, {'id': 'D011787', 'term': 'Quality of Health Care'}, {'id': 'D006298', 'term': 'Health Services Administration'}, {'id': 'D017530', 'term': 'Health Care Quality, Access, and Evaluation'}]}}, 'protocolSection': {'designModule': {'phases': ['NA'], 'studyType': 'INTERVENTIONAL', 'designInfo': {'allocation': 'RANDOMIZED', 'maskingInfo': {'masking': 'NONE'}, 'primaryPurpose': 'SUPPORTIVE_CARE', 'interventionModel': 'SINGLE_GROUP'}, 'enrollmentInfo': {'type': 'ACTUAL', 'count': 53}}, 'statusModule': {'overallStatus': 'COMPLETED', 'startDateStruct': {'date': '2007-08'}, 'expandedAccessInfo': {'hasExpandedAccess': False}, 'statusVerifiedDate': '2017-11', 'completionDateStruct': {'date': '2012-04', 'type': 'ACTUAL'}, 'lastUpdateSubmitDate': '2017-11-29', 'studyFirstSubmitDate': '2012-05-04', 'studyFirstSubmitQcDate': '2012-05-07', 'lastUpdatePostDateStruct': {'date': '2017-12-02', 'type': 'ACTUAL'}, 'studyFirstPostDateStruct': {'date': '2012-05-08', 'type': 'ESTIMATED'}, 'primaryCompletionDateStruct': {'date': '2012-04', 'type': 'ACTUAL'}}, 'outcomesModule': {'primaryOutcomes': [{'measure': 'Cancer Knowledge Survey', 'timeFrame': 'Time of Enrollment and 9 Months Later', 'description': 'Measure of patient reported knowledge of their cancer diagnosis, history and treatments.'}], 'secondaryOutcomes': [{'measure': 'SF-36 Questionnaire', 'timeFrame': 'Time of Enrollment and 9 Months Later', 'description': 'A measure of quality of life.'}, {'measure': 'Cancer Rehabilitation Evaluation System', 'timeFrame': 'Time of Enrollment and 9 Months Later', 'description': 'Short Form (SF) Medical Interaction Subscale'}, {'measure': 'Herth Hope Index', 'timeFrame': 'Time of Enrollment and 9 Months Later', 'description': 'A measure of self-reported hope.'}, {'measure': 'Multidimensional Scale of Perceived Social Support', 'timeFrame': 'Time of Enrollment and 9 Months Later', 'description': 'A measure of self-reported social support.'}, {'measure': 'Health Locus of Control Scale', 'timeFrame': 'Time of Enrollment and 9 Months Later', 'description': 'A measure of self-reported locus of control.'}, {'measure': 'State Trait Anxiety Inventory', 'timeFrame': 'Time of Enrollment and 9 Months Later', 'description': 'A measure of self-reported anxiety.'}]}, 'oversightModule': {'oversightHasDmc': False}, 'conditionsModule': {'keywords': ['cancer survivor'], 'conditions': ['Cancer Survivor']}, 'descriptionModule': {'briefSummary': 'This is a randomized controlled trial of a web-based informational intervention (UMFollowUp) for adolescent and young adult survivors of childhood cancer to improve cancer knowledge and psychosocial functioning.', 'detailedDescription': 'Individuals randomly assigned to the control group will receive standard of care for the duration of their participation. This means they will continue to receive information regarding their diagnosis, treatments and ongoing health needs from their provider (no access to website).\n\nIndividuals randomly assigned to the treatment group will receive access to UMFollowUp, a secure, HIPAA-compliant website.\n\nAll participants will be asked to complete paper-and-pencil surveys at baseline and 9 months later to determine the impact of the web-based intervention.'}, 'eligibilityModule': {'sex': 'ALL', 'stdAges': ['CHILD', 'ADULT'], 'maximumAge': '28 Years', 'minimumAge': '15 Years', 'healthyVolunteers': False, 'eligibilityCriteria': 'Inclusion Criteria:\n\n* History of diagnosis of hematologic malignancy or malignant neoplasm, and in disease free remission at time of recruitment.\n* Must be English-speaking and have access to a computer with internet access, and must have completed treatment at University of Minnesota Medical Center-Fairview for cancer.\n\nExclusion Criteria:\n\n* Individual with significant visual impairments and neurologic/cognitive difficulties which limit their ability to see and under our outcome questionnaires or website content will be excluded from participation.'}, 'identificationModule': {'nctId': 'NCT01593618', 'briefTitle': 'Empowering Cancer Survivors Through Information Technology', 'organization': {'class': 'OTHER', 'fullName': 'Masonic Cancer Center, University of Minnesota'}, 'officialTitle': 'Empowering Cancer Survivors Through Information Technology', 'orgStudyIdInfo': {'id': '2007NT078'}}, 'armsInterventionsModule': {'armGroups': [{'type': 'EXPERIMENTAL', 'label': 'Web-Based Intervention', 'description': 'UMFollowUp - web-based internet resource for information about their diagnostic histories, recommendations for follow-up care, and tips to enhance their treatment, psychosocial and physical well-being.', 'interventionNames': ['Behavioral: UMFollowUp']}, {'type': 'ACTIVE_COMPARATOR', 'label': 'Standard of Care', 'description': 'Patients will receive information regarding their diagnosis, treatments, and ongoing health needs from their provider, but will not be provided access to the website.', 'interventionNames': ['Other: Standard of Care']}], 'interventions': [{'name': 'UMFollowUp', 'type': 'BEHAVIORAL', 'description': 'Web-based internet resource for self-reported treatment summaries and psychosocial and physical well-being.', 'armGroupLabels': ['Web-Based Intervention']}, {'name': 'Standard of Care', 'type': 'OTHER', 'description': 'Patients will receive information regarding their diagnosis, treatments, and ongoing health needs from their provider, but will not be provided access to the website.', 'armGroupLabels': ['Standard of Care']}]}, 'contactsLocationsModule': {'locations': [{'zip': '55455', 'city': 'Minneapolis', 'state': 'Minnesota', 'country': 'United States', 'facility': 'Masonic Cancer Center, University of Minnesota', 'geoPoint': {'lat': 44.97997, 'lon': -93.26384}}], 'overallOfficials': [{'name': 'Alicia Kunin-Batson, M.D.', 'role': 'PRINCIPAL_INVESTIGATOR', 'affiliation': 'Masonic Cancer Center, University of Minnesota'}]}, 'sponsorCollaboratorsModule': {'leadSponsor': {'name': 'Masonic Cancer Center, University of Minnesota', 'class': 'OTHER'}, 'responsibleParty': {'type': 'SPONSOR'}}}}