Completed

CII-CPPIntegrative Interventions for Chronic Pelvic Pain

What is being tested

My Pelvic Plan

+ Bend

DeviceBehavioral

Who is being recruted

Neurologic Manifestations+2

+ Pain

+ Signs and Symptoms

From 18 to 55 Years

+10 Eligibility Criteria

See all eligibility criteria

How is the trial designed

Treatment Study

Interventional

Study Start: August 2025

See protocol details

Summary

Principal SponsorSara Till, MD, MPH

Last updated: January 30, 2026

Sourced from a government-validated database.Claim as a partner

Study start date: August 12, 2025

Actual date on which the first participant was enrolled.

This study focuses on testing different integrative treatment methods for individuals who experience chronic pelvic pain. Chronic pelvic pain is a condition that affects many people, often leading to discomfort and affecting daily life. The aim is to find effective ways to alleviate this pain using various approaches. This is significant because current treatments might not work for everyone, and finding new strategies could greatly improve the quality of life for those affected. Participants in this study will undergo different treatment methods to see which provides the best relief from pelvic pain. The study will use "My Pelvic Plan," recognized as a medical device under FDA enforcement discretion. Although specific procedures and measurements are not detailed, the study will likely assess changes in pain levels and overall wellbeing. By comparing the outcomes of these interventions, researchers hope to identify the most effective options for managing chronic pelvic pain.

Official TitleComparing Integrative Interventions for Chronic Pelvic Pain

NCT07066345

Principal SponsorSara Till, MD, MPH

Last updated: January 30, 2026

Sourced from a government-validated database.Claim as a partner

Protocol

This section provides details of the study plan, including how the study is designed and what the study is measuring.

Design Details

49 patients to be enrolled

Total number of participants that the clinical trial aims to recruit.

Treatment Study

These studies test new ways to treat a disease, condition, or health issue. The goal is to see if a new drug, therapy, or approach works better or has fewer side effects than existing options.

Eligibility

Researchers look for people who fit a certain description, called eligibility criteria: person's general health condition or prior treatments.

Conditions

Criteria

Female

Biological sex of participants that are eligible to enroll.

From 18 to 55 Years

Range of ages for which participants are eligible to join.

Healthy volunteers not allowed

If individuals who are healthy and do not have the condition being studied can participate.

Conditions

Pathology

Neurologic ManifestationsPainSigns and SymptomsPathological Conditions, Signs and SymptomsPelvic Pain

Criteria

6 inclusion criteria required to participate

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

Show More Criteria

4 exclusion criteria prevent from participating

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).

Study Plan

Find out more about all the medication administered in this study, their detailed description and what they involve.

Treatment Groups

Study Objectives

2 intervention groups are designated in this study

This study does not include a placebo group

Treatment Groups

Group I

Experimental

Patients will be randomized to receive one of two non-pharmacologic interventions. Group 1 will receive access to a novel web-based, cognitive behavioral program.

Group II

Active Comparator

Patients will be randomized to receive one of two non-pharmacologic interventions. Group 2 will receive a subscription to a commercially available remote application.

Study Objectives

Primary Objectives

Secondary Objectives

Study Centers

These are the hospitals, clinics, or research facilities where the trial is being conducted. You can find the location closest to you and its status.

This study has 1 location

Suspended

University of Michigan

Ann Arbor, United StatesOpen University of Michigan in Google Maps

CompletedOne Study Center