Development and Evaluation of a Screening Approach for Sexual Dysfunction in AYA Patients With and Surviving Childhood Cancer

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age15-24
SponsorUniversity of Colorado, Denver

About this trial

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.

Eligibility criteria

Qualifiers

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)

Disqualifiers

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

Trial design

Treatments tested in this trial

  • Sexual Function Screening Approach

Treatment groups

205 Participants
are divided into 2 treatment groups

Sponsors and collaborators

University of Colorado, Denver

Lead sponsor

National Cancer Institute (NCI)

Collaborator