Comprehensive Care for AYA: Needs Assessment Survey

NCT ID: NCT07196241

Last Updated: 2026-01-28

Study Results

Results pending

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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Recruitment Status

NOT_YET_RECRUITING

Total Enrollment

300 participants

Study Classification

OBSERVATIONAL

Study Start Date

2026-03-31

Study Completion Date

2026-10-31

Brief Summary

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The goal of this observational study is to assess gaps in education about exercise, sexual health, fertility, survivorship, financial issues, interpersonal relationships, and clinical trial participation among adolescents and young adults with cancer.

Participants will be asked to complete a series of questionnaires.

Detailed Description

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This descriptive study aims to assess current needs of adolescents and young adults with cancer.

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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Cancer Young Adult Cancer Adolescent Cancer

Study Design

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Observational Model Type

OTHER

Study Time Perspective

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.

Intervention Type OTHER

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.

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

* Individuals diagnosed with cancer between the ages of 15-39 per self-report. Participants may be enrolled at any age provided diagnosis was between ages 15-39.
* 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

* Severe emotional distress or anxiety that would limit compliance with study requirements per self-report.
Minimum Eligible Age

15 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Atrium Health Wake Forest Baptist

OTHER

Sponsor Role collaborator

Wake Forest University Health Sciences

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

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

Site Status

Atrium Health Wake Forest Baptist Comprehensive Cancer Center

Winston-Salem, North Carolina, United States

Site Status

Countries

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United States

Central Contacts

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Anne Wofford, MD

Role: CONTACT

336-716-3684

Facility Contacts

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Erin Trovillion, MD

Role: primary

704-381-9900

Anne Wofford, MD

Role: primary

336-716-3684

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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