NCT07810218Recruiting
Personalized Exercise Recommendations for Chronic Pelvic Pain Using Reinforcement Learning
WorkoutCPP: A Pilot Series of N-of-1 Trials Evaluating RL-Generated Adaptive Exercise Recommendations for Pelvic Pain Management
Source: ClinicalTrials.gov · Last updated 9 Sept 2026
Brief summary (registry, in English)
WorkoutCPP is a pilot study evaluating the feasibility of a personalized exercise recommendation system for individuals with chronic pelvic pain disorders (CPPDs). The study uses reinforcement learning (RL), a type of artificial intelligence that adapts recommendations over time based on each participant's reported pain levels, symptom burden, and exercise compliance. Participants receive daily exercise recommendations that alternate between standard, non-personalized guidance and personalized, RL-generated recommendations across four 2-week phases, allowing within-person comparison of outcomes under each condition. The primary hypothesis is that an RL-based adaptive recommendation system is feasible to deliver in a CPPD population.
- Status (registry)
- Recruiting
- Study type
- Interventional
- Enrollment
- 45 (estimated)
- First submitted
- 3 Sept 2026
- Start date
- 6 Feb 2026
- Primary completion date
- Aug 2027
- Lead sponsor
- Icahn School of Medicine at Mount Sinai
- Diseases
- Endometriosis
- NCT number
- NCT07810218
What you commit to
- Study type: Interventional
- Planned participants: 45
- From 6 Feb 2026 to the primary completion date, Aug 2027
- 1 site in 1 country
- Visits and tests: ask the trial team, the registry does not list them
Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.
Who cannot take part
Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.
Prior treatment
- Major life events expected during the next 10 weeks (e.g., pregnancy, planned surgery, or extended travel likely to interfere with participation).
Other illness
- Absolute contraindications to PA (e.g., recent myocardial infarction, complete heart block, acute congestive heart failure, unstable angina, or uncontrolled severe hypertension, BP ≥180/110 mm Hg).
Lab values
- More than two "Yes" responses on the Physical Activity Readiness Questionnaire (PAR-Q) (16) without physician clearance.
Other
- Current or planned pregnancy within the next 6 months.
- Having given birth in the past 6 months or currently nursing.
- Inability to wear an activity tracker or use the app for the study duration.
- Complete inactivity (i.e., \<60 minutes of moderate-intensity PA per week).
Who the study is looking for
- Self-reported CPPD (e.g., endometriosis, adenomyosis, fibroids, etc.) based on clinician diagnosis
- Aged 18-55 years.
- Ownership of an iOS or Android smartphone.
- Willingness to self-track daily symptoms, exercise activities, and self-management behaviors using a smartphone research app.
- Willingness to wear an activity tracker for the study duration.
- Willingness to follow exercise recommendations from a smartphone research app, provided no adverse symptoms occur.
- Ability to read and write in English sufficient to understand study materials and communications.
- At least intermittently physically active (e.g., ≥30 minutes of walking twice per week).
Age in the registry: 18 years to 55 years · Sex: Female · Does not accept healthy volunteers
Sites (1)
Sites in registry order. Pick your city on the disease page to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| Icahn School of Medicine at Mount Sinai Coordinator of this site? Confirm its status | New York | United States | Recruiting |
This page is information, not medical advice. Discuss any trial with your doctor.