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NCT Number: NCT07196241

Comprehensive Care for AYA: Needs Assessment Survey

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.

Recruiting

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Key information

Age range

15 year and older

Sex eligibility

All sexes

Study type

Observational

Primary location

Atrium Health Levine Cancer, Charlotte, North Carolina, United States

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About this study

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).

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

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.

Treatment and study plan

Survey using a questionnaire.

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.

Primary outcomes

  1. Deficits in Education

    Time frame: At study enrollment

    The general information survey collects data on participants surrounding education on health-related topics, gender, and sexual orientation, as well as perceived needs for resources, support areas, programs and activities. The general information survey contains 12 items.

    There is no formal statistical analysis to be performed only summary statistics on completed survey items for observation thus there is no scoring needed or range of scores. Results will be observed using descriptive statistics. Due to the categorical nature of all variables, results will be reported in frequencies and percentages.

  2. Preferred Format for Education

    Time frame: At study enrollment

    The General Information Survey collects data on participants surrounding education on health-related topics, gender, and sexual orientation, as well as perceived needs for resources, support areas, programs and activities. The general information survey contains 12 items.

    There is no formal statistical analysis to be performed only summary statistics on completed survey items for observation thus there is no scoring needed or range of scores. Results will be observed using descriptive statistics. Due to the categorical nature of all variables, results will be reported in frequencies and percentages.

Other outcomes

  1. Deficit in Education by Covariates

    Time frame: At study enrollment

    Data on covariates will be collected with the Patient Demographic Information survey, Cancer History survey, Treatment Status and Follow-up Care survey, Fertility Preservation survey , Emotional Health and Interpersonal Relationships survey, Financial Burden survey and the Clinical Trial Participation Questionnaire.

    There is no formal statistical analysis to be performed only summary statistics on completed survey items for observation thus there is no scoring needed or range of scores. Results will be observed using cross tabulations reported in frequencies and percentages.

  2. Focus Group Interest

    Time frame: At study enrollment

    Patients interested in serving on the AYA focus group will be identified using the single-item Interest in Focus Group Survey to provide contact information for a future focus group outside of this study.

    Results will be reported as binary (yes/no) for participation in the focus group via frequency and percentage.

Study contacts

Contact information is provided by the study sponsor or research team.

Anne Wofford, MD

CONTACT

[email protected]

336-716-3684

Sponsors and collaborators

Lead sponsor

Wake Forest University Health Sciences

Other

Collaborators

  • Atrium Health Wake Forest Baptist
  • National Cancer Institute (NCI)

Registry information

Important dates

Study start
2026
Primary completion
2026
Study completion
2026
First posted
Sep 29, 2025
Registry last updated
May 26, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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