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Comparing Integrative Interventions for Chronic Pelvic Pain

CompletedNot applicableNCT07066345
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 researchers will conduct a pilot randomized trial to assess functional changes with two different remote integrative non-pharmacologic interventions for women with chronic pelvic pain (CPP). The study team will compare a novel web-based, cognitive-behavioral program designed for patients with CPP and a commercially available physical activity remote application. The team aims to gather information about differences in sexual function, physical function, pain, and quality of life.

Study details

Official title
Comparing Integrative Interventions for Chronic Pelvic Pain
Conditions
Interventions
  • Device: My Pelvic Plan
  • Behavioral: Bend
Sponsor
Sara Till, MD, MPH
Collaborators
Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD)
Organization
University of Michigan
Start date
2025-08-12
Primary completion
2026-01-19
Sex
Female
Age range
from 18 Years to 55 Years
Results posted
No results posted in this snapshot
Countries
United States
Total sites listed
1

Eligibility criteria

Show eligibility criteria (verbatim from the registry)
Inclusion Criteria: * Scheduled for a new patient visit with the Chronic Pelvic Pain and Endometriosis Referral Clinic within the Department of Obstetrics and Gynecology at the University of Michigan for treatment of chronic pelvic pain. * Have chronic pelvic pain, defined as moderate to severe pelvic pain that is ≥ 4 on a 0-10 numeric rating scale (worst pain during the day) for ≥ 6-month duration, and is non-cyclic, occurring for at least 14 days of each month. * Report moderate to severe sexual dysfunction or sexual restriction on CPP clinic intake questionnaire. This will be defined as the patient indicating one of the following responses to a question that asks them to describe their experience relative to sexual activity: my sex life is nearly normal but is very painful, my sex life is severely restricted by pain, my sex life is nearly absent because of pain, pain prevents any self life at all. * Have access to internet via computer and must have a smartphone * Willing to download and use the Bend application on their smartphone if they are randomized to that intervention * English-language proficiency (current version of the My Pelvic Plan website is in English) Exclusion Criteria: * Pregnancy (at time of screening visit). Participants will be allowed to continue to study if they become pregnant during the study period. * Severe physical impairment precluding participating in internet-based program or remote application (for example, complete blindness or deafness) * Medical condition that precludes low-intensity, short-duration physical activity and gentle stretching, including cerebral palsy, severe hip or knee osteoarthritis, severe heart failure, severe Chronic obstructive pulmonary disease (COPD) requiring oxygen use * Prior care within the Chronic Pelvic Pain and Endometriosis Referral Clinic within the Department of Obstetrics and Gynecology at the University of Michigan for treatment of chronic pelvic pain (seen previously but meets criteria for new patient visit because \> 3 year interval since last clinic visit).

Source: ClinicalTrials.gov (US National Library of Medicine), snapshot October 2026. Check the registry for current recruiting status. Record: https://clinicaltrials.gov/study/NCT07066345