Actively Recruiting
Development and Evaluation of a Screening Approach for Sexual Dysfunction in AYA Patients With and Surviving Childhood Cancer
Led by University of Colorado, Denver · Updated on 2026-05-06
205
Participants Needed
2
Research Sites
228 weeks
Total Duration
On this page
Sponsors
U
University of Colorado, Denver
Lead Sponsor
N
National Cancer Institute (NCI)
Collaborating Sponsor
AI-Summary
What this Trial Is About
Prior research determined adolescent and young adult-aged childhood cancer survivor (AYA-CCS) and medical provider acceptability of the SexFS Brief in a controlled research setting. Development of an acceptable, effective, and feasible screening approach will result in improved recognition of SD in AYA patients with and surviving childhood cancer.
CONDITIONS
Official Title
Development and Evaluation of a Screening Approach for Sexual Dysfunction in AYA Patients With and Surviving Childhood Cancer
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Provide signed and dated consent form
- Willingness to comply with all study procedures and available for the study duration
- Aged 15 to 24 years at enrollment
- Diagnosed with cancer before age 18 as listed in the International Classification of Diseases for Oncology (ICD-O) with behavior code ≥2
- Received cancer-directed therapy including chemotherapy, radiotherapy, or surgery (biopsies excluded)
- Have an appointment at one of the four specified clinical sites: CHCO HOPE Survivorship Program, CHCO Oncology Clinic, CHCO Neuro-Oncology Clinic, or Seattle Children's Hospital Survivorship Program
You will not qualify if you...
- Unable to read and speak English
- Did not receive cancer-directed therapy
- Insufficient cognitive functioning to complete study measures
- Participated in intervention development
- Patient is at end of life or on hospice, as determined by primary oncologist
- Did not undergo sexual function screening within 1 month of being due (for implementation outcomes measurement)
AI-Screening
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Trial Site Locations
Total: 2 locations
1
Childrens Hospital Colorado
Aurora, Colorado, United States, 80045
Actively Recruiting
2
University of Colorado Hospital
Aurora, Colorado, United States, 80045
Actively Recruiting
Research Team
B
Barbara Shepperd
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
NON_RANDOMIZED
Model
SEQUENTIAL
Primary Purpose
SUPPORTIVE_CARE
Number of Arms
2
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