AYA OMGYES Sexual Health Study
For patients and families
In plain language
An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.
- What is being studied
- The protocol lists: OMGYES.com.
- Who it may be relevant to
- Registry conditions: Sexual Dysfunction. Basic parameters: 18 years — 45 years · Female.
- What needs checking
- Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
- Where it takes place
- United States
- Next step
- Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Unsure about the terms? Read our patient guide →
Official title
Assessing the Impact of a Web-based Educational Program on the Sexual Health Outcomes of Young Adult Female Cancer Survivors ~ A Pilot Trial
Overview
The purpose of this study is to assess the impact of the web-based intervention OMGYES.com on sexual dysfunction in young adult (YA) female-bodied cancer survivors. This pilot trial seeks to evaluate the intervention's: * feasibility * acceptability * appropriateness. Researchers will utilize an active observation period to compare outcomes between those receiving the intervention immediately and those who haven't Participants will: * Complete online modules at home * Visit the clinic every 5 weeks for questionnaires
Interventions
- Other OMGYES.com
OMGYES.com is an interactive website that offers information, video tutorials, interviews, tips, and resources to explore female sexual pleasure through groundbreaking research that's told through the real-life experiences of women of all ages and life stages.
Primary outcome measures
- Feasibility of OMGYES.com using the Feasibility of Intervention Measure (FIM) [Time frame: End of Study (Week 6)]
Secondary outcome measures (2)
- Acceptability of OMGYES.com using the Acceptability of Intervention Measure (AIM) [Time frame: End of Study (Week 6)]
- Appropriateness of OMGYES.com using the Appropriateness of Intervention Measure [Time frame: End of Study (Week 6)]
Eligibility criteria
Inclusion criteria
- 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 a prior or concurrent malignancy whose natural history or treatment does not have the potential to interfere with the safety or efficacy assessment of the investigational regimen are eligible for this trial
- Ability to participate in study modules and to respond to surveys
- Ability to understand and the willingness to sign a written informed consent document
Exclusion criteria
- Patients receiving other investigational agents
- Patients expected to be neutropenic or have a significantly high infection risk that would exclude them from vaginal penetration
- Patients who are unable complete the study intervention or surveys
Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.
Healthy volunteers: No
Study design
- Allocation
- Randomized
- Model
- Parallel assignment
- Masking
- Open label
- Primary purpose
- Supportive care
Study locations
United States · 1 center
- University of Chicago Hospital — Chicago
Identifiers
NCT: NCT06868121 · IRB24-0909