Actively Recruiting
Assessing the Impact of a Web-based Educational Program on the Sexual Health Outcomes of Young Adult Female Cancer Survivors ~ A Pilot Trial
Led by University of Chicago · Updated on 2026-06-05
30
Participants Needed
1
Research Sites
13 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
Researchers are evaluating the effects of the web-based program OMGYES.com on sexual dysfunction in young adult female cancer survivors. This pilot trial aims to assess how feasible, acceptable, and appropriate the intervention is for this group. The study compares outcomes between participants who receive the intervention immediately and those who begin it after a period of observation. Participants will be assigned to one of two groups: an immediate intervention group that starts using OMGYES.com right after enrollment, and a delayed intervention group that undergoes 5 weeks of observation before starting the program. The intervention consists of completing online educational modules at home. During the study, participants will visit the clinic every 5 weeks to complete questionnaires assessing feasibility, acceptability, and appropriateness of the intervention using standardized measures. The main outcome will be measured at the end of the 6-week study period. The trial runs through November 2026 and involves young adult female cancer survivors aged 18 to 45 years.
CONDITIONS
Brief Title
AYA OMGYES Sexual Health Study
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Age 18 to 45 years
- Diagnosis of cancer between the ages of 15 and 45
- Female genitalia, regardless of gender
- Diagnosed with sexual dysfunction
- Complete remission and at least two months from a major treatment
- Patients with prior or concurrent malignancy that does not interfere with safety or efficacy assessment
- Ability to participate in study modules and respond to surveys
- Ability to understand and willingness to sign informed consent
You will not qualify if you...
- Receiving other investigational agents
- Expected to be neutropenic or have a high infection risk excluding vaginal penetration
- Unable to complete the study intervention or surveys
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person or remote)
Duration - 5 weeks
Participants in the delayed intervention group undergo 5 weeks of active observation prior to receiving the intervention.
Regular assessments during observation period as per study schedule
Duration - Up to 6 weeks
Participants receive access to the OMGYES.com web-based educational program to support sexual health outcomes.
1 baseline visit and follow-up visits during intervention
Trial Site Locations
Total: 1 location
1
University of Chicago Hospital
Chicago, Illinois, United States, 60637
Actively Recruiting
Research Team
C
Cassandra Kuissi, BS
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
SUPPORTIVE_CARE
Number of Arms
2
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