New screening tool aims to break the silence on sexual health after childhood cancer
NCT ID NCT05524610
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study tests a simple questionnaire to help doctors identify sexual health concerns in teenagers and young adults who have or had childhood cancer. The goal is to improve communication between patients and providers. About 205 participants aged 15-24 will use the screening tool during clinic visits, and researchers will measure whether it leads to more discussions about sexual function.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Sexual function screening questionnaire (PROMIS SexFS Brief)
- What this could lead to
- If successful, this screening approach could become a standard way for doctors to identify and discuss sexual health issues with young cancer survivors, leading to better support and quality of life.
- What could go wrong
- This is a small, early-stage study focused on feasibility and communication, not on treating sexual dysfunction. The screening tool may not work well in all clinic settings or for all patients.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
-
Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
-
About 205 people
The number the study aims to enrol. It can still change while the study runs.
- Started
-
Feb 2023
- Expected to finish
-
Jun 2027
An estimate. End dates often move.
- Lead sponsor
-
Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
-
15 to 24 years
- Sex
-
Anyone
- Healthy volunteers
-
Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria In order to be eligible to participate in this study, an individual must meet all of the following criteria: 1. Provision to sign and date the consent form. 2. Stated willingness to comply with all study procedures and be available for the duration of the study. 3. Be aged 15-24 years old at the time of enrollment 4. 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) 5. Must have received cancer-directed therapy with at least one of the following: * Chemotherapy: any anticancer drug to treat the cancer diagnosis including immunotherapy * Radiotherapy: any radiotherapy to treat the cancer diagnosis * Surgery: any surgery to remove cancer including partial or total resections. Biopsies are not considered surgery. 6. Cancer must have been diagnosed before the age of 18 years 7. 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 An individual who meets any of the following criteria will be excluded from participation in this study: 1. Unable to read and speak English 2. Patients who did not receive cancer-directed therapy 3. Insufficient cognitive functioning to complete study measures, as determined by patient's 4. Participation in intervention development 5. Patient is at end of life or on hospice, as determined by primary oncologist 6. Patients who did not undergo sexual function screening within 1 month of being due will be excluded from implementation outcomes measurement 7. Patient is at end of life or on hospice, as determined by primary oncologist
Get updates
Get notified about this study
Sign up to get updates when this study changes or when new studies for Pediatric cancer are added.
By submitting, you agree to our Terms of use
Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
How to take part
Only the study team decides who joins. These are the ways to reach them.
-
The places running it
2 sites. The list below names each one and where it is.
-
The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
-
A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Locations
-
Childrens Hospital Colorado
RECRUITINGAurora, Colorado, 80045, United States
-
University of Colorado Hospital
RECRUITINGAurora, Colorado, 80045, United States
More trials for these conditions
Other studies related to the condition(s) this trial covers.
- Can freezing ovarian tissue protect fertility in children facing cancer treatment?
- Tumor profiling may unlock targeted drug options for pediatric cancers
- Can a new pill tame childhood cancers that Won't quit?
- A bike ride could reveal hidden heart risks in young cancer survivors
- Talking therapy may offer a path away from opioids for cancer survivors
- Can a new combo drug tame childhood leukemia that Won't quit?