Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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NOT_YET_RECRUITING
300 participants
OBSERVATIONAL
2026-03-31
2026-10-31
Brief Summary
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Participants will be asked to complete a series of questionnaires.
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Detailed Description
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Participants who were diagnosed with cancer between the ages of of 15-39 will be asked to complete questionnaires to provide information on their cancer treatments and follow-up care, fertility preservation, clinical trial participation, emotional health and interpersonal relationships, financial burden, mental health and additional general information (health related, sexual orientation, perceived needs for support, resources, programs and activities).
Conditions
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Study Design
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OTHER
CROSS_SECTIONAL
Study Groups
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Adolescents and Young Adults with cancer
Participants diagnosed with cancer between the ages of 15-39 who have received or are receiving cancer-directed treatment at one of the participating centers per self-report.
Survey using a questionnaire.
Questionnaires regarding cancer treatment and follow-up care, fertility preservation, clinical trial participation, general information (education on health- related topics, gender, and sexual orientation, perceived needs for resources, support areas, programs and activities.), emotional health and interpersonal relationships, financial burden and mental health status.
Interventions
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Survey using a questionnaire.
Questionnaires regarding cancer treatment and follow-up care, fertility preservation, clinical trial participation, general information (education on health- related topics, gender, and sexual orientation, perceived needs for resources, support areas, programs and activities.), emotional health and interpersonal relationships, financial burden and mental health status.
Eligibility Criteria
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Inclusion Criteria
* Individuals who have received or are receiving cancer-directed treatment (chemotherapy, immunotherapy, surgery and/or radiation) at one of the participating centers per self-report.
Exclusion Criteria
15 Years
ALL
No
Sponsors
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Atrium Health Wake Forest Baptist
OTHER
Wake Forest University Health Sciences
OTHER
Responsible Party
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Principal Investigators
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Anne Wofford, MD
Role: PRINCIPAL_INVESTIGATOR
Atrium Health Wake Forest Baptist
Locations
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Atrium Health Levine Cancer
Charlotte, North Carolina, United States
Atrium Health Wake Forest Baptist Comprehensive Cancer Center
Winston-Salem, North Carolina, United States
Countries
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Central Contacts
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Facility Contacts
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Other Identifiers
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ONC-CCS-2505
Identifier Type: OTHER
Identifier Source: secondary_id
IRB00136539
Identifier Type: -
Identifier Source: org_study_id
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