NCT06352840Completed
Novel Web-based, Self-directed Intervention for Chronic Pelvic Pain
Source: ClinicalTrials.gov · Last updated 13 Feb 2026
Brief summary (registry, in English)
The study is being completed to evaluate the effectiveness of a web-based, self-management program for patients with Chronic Pelvic Pain (CPP). The overall hypothesis is that patients with chronic pelvic pain that have access to the My Pelvic Plan program will demonstrate improvements in pain, physical function, and quality of life with this integrative self-management approach.
- Status (registry)
- Completed
- Study type
- Interventional
- Enrollment
- 70 (actual)
- First submitted
- 2 Apr 2024
- Start date
- 20 Jun 2024
- Primary completion date
- 23 Jan 2025
- Lead sponsor
- University of Michigan
- Diseases
- Endometriosis
- NCT number
- NCT06352840
What you commit to
- Study type: Interventional
- Participants enrolled: 70
- From 20 Jun 2024 to the primary completion date, 23 Jan 2025
- 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
- Underwent gynecologic surgery within 3 months of screening visit
- Plan to undergo gynecologic surgery within 6 months following screening visit
Other illness
- Severe physical impairment precluding participating in internet-based program (for example, complete blindness or deafness)
- Current psychiatric disorder with history of psychosis (for example, schizophrenia, schizoaffective disorder, delusional disorder),
Other
- Pregnant (self-reported) at time of screening visit. Will not exclude patients that become pregnant during the course of the study.
- Current suicidal ideation or suicide attempt within 2 years of screening visit. The study will screen for severe depression and suicidality at each questionnaire time point and have developed a robust triage and referral plan.
Who the study is looking for
- Participants have chronic pelvic pain, defined by the protocol for ≥ 6-month duration, and is non-cyclic, occurring for at least 14 days of each month.
- Must be currently receiving care within Department of Obstetrics and Gynecology at the University of Michigan for treatment of chronic pelvic pain
- Access to internet via computer or smartphone
- English-language proficiency (current version of the website is in English)
Age in the registry: 18 years to - · 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 |
|---|---|---|---|
| University of Michigan Coordinator of this site? Confirm its status | Ann Arbor | United States | Unknown status |
This page is information, not medical advice. Discuss any trial with your doctor.