Development and Evaluation of a Screening Approach for Sexual Dysfunction in AYA Patients With an… (NCT05524610) | Clinical Trial Compass
RecruitingNot Applicable
Development and Evaluation of a Screening Approach for Sexual Dysfunction in AYA Patients With and Surviving Childhood Cancer
United States205 participantsStarted 2023-02-14
Plain-language summary
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.
Who can participate
Age range15 Years – 24 Years
SexALL
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AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Inclusion criteria
✓. Provision to sign and date the consent form.
✓. Stated willingness to comply with all study procedures and be available for the duration of the study.
✓. Be aged 15-24 years old at the time of enrollment
✓. Patients with or surviving of cancer (must be found in the International Classification of Diseases for Oncology (ICD-O) and have a behavior code ≥2)
✓. Must have received cancer-directed therapy with at least one of the following:
✓. Cancer must have been diagnosed before the age of 18 years
✓. Patient must have an appointment at one of four clinical sites: CHCO HOPE Survivorship Program, CHCO Oncology Clinic, CHCO Neuro-Oncology Clinic, Seattle Children's Hospital Survivorship Program
Exclusion criteria
✕. Unable to read and speak English
✕. Patients who did not receive cancer-directed therapy
✕. Insufficient cognitive functioning to complete study measures, as determined by patient's
✕. Participation in intervention development
✕. Patient is at end of life or on hospice, as determined by primary oncologist
✕
What they're measuring
1
Comparison of sexual function communication before and after intervention implementation