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Clinical Trials/NCT07196241
NCT07196241RecruitingNot Applicable

Comprehensive Care for AYA: Needs Assessment Survey

Wake Forest University Health Sciences2 sites in 1 country300 target enrollmentStarted: April 16, 2026Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Recruiting
Enrollment
300
Locations
2
Primary Endpoint
Deficits in Education

Study Overview

Brief Summary

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

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).

Study Design

Study Type
Observational
Observational Model
Other
Time Perspective
Cross-sectional

Eligibility Criteria

Ages
15 Years to — (Child, Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

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.

Arms & Interventions

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.

Intervention: Survey using a questionnaire. (Other)

Outcomes

Primary Outcomes

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.

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.

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor Class
Other
Responsible Party
Sponsor

Study Sites (2)

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Identifiers

NCT ID
NCT07196241
Other Study IDs
IRB00136539, P30CA012197, ONC-CCS-2505

Dates

First Submitted
(last year)
First Posted
(last year)
Primary Completion
(in 13 hours)
Study Completion
(in 2 months)
Last Verified
(2 months ago)
Last updated
(last month)

Regulatory & Sharing

FDA Regulated Drug
No
FDA Regulated Device
No
IPD Sharing Plan
No
Has Results
No

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