Novel Web-based, Self-directed Intervention for Chronic Pelvic Pain
CompletedNot applicableNCT06352840
View the official record on ClinicalTrials.gov Recruiting status changes often. Contact the study team listed on ClinicalTrials.gov, and talk to your doctor before joining a study.
This study has no listed site in Canada in this snapshot. It is included as part of the worldwide chronic pain corpus.
Brief summary (from the registry)
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.
Study details
- Official title
- Novel Web-based, Self-directed Intervention for Chronic Pelvic Pain
- Conditions
- Interventions
- Behavioral: My Pelvic Plan Website
- Behavioral: Control Group website
- Sponsor
- University of Michigan
- Collaborators
- Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD)
- Start date
- 2024-06-20
- Primary completion
- 2025-01-23
- Sex
- Female
- Age range
- from 18 Years
- Results posted
- Yes, on ClinicalTrials.gov
- Countries
- United States
- Total sites listed
- 1
Eligibility criteria
Show eligibility criteria (verbatim from the registry)
Inclusion Criteria: * 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) Exclusion Criteria: * Underwent gynecologic surgery within 3 months of screening visit * Plan to undergo gynecologic surgery within 6 months following screening visit * Pregnant (self-reported) at time of screening visit. Will not exclude patients that become pregnant during the course of the study. * 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), * 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.
Source: ClinicalTrials.gov (US National Library of Medicine), snapshot October 2026. Check the registry for current recruiting status. Record: https://clinicaltrials.gov/study/NCT06352840