Clinical Trials Directory

Trials / Completed

CompletedNCT07066345

Comparing Integrative Interventions for Chronic Pelvic Pain

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
49 (actual)
Sponsor
Sara Till, MD, MPH · Academic / Other
Sex
Female
Age
18 Years – 55 Years
Healthy volunteers
Not accepted

Summary

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.

Detailed description

My Pelvic Plan was determined as a medical device under FDA enforcement discretion.

Conditions

Interventions

TypeNameDescription
DEVICEMy Pelvic PlanMy Pelvic Plan is comprised of a self-guided program that combines education on several individual conditions that often contribute to CPP, and will include instruction on cognitive and behavioral restructuring techniques that can help to manage chronic pelvic pain symptoms.
BEHAVIORALBendBend is a highly rated physical activity application that helps guide users through gentle stretching and yoga poses.

Timeline

Start date
2025-08-12
Primary completion
2026-01-19
Completion
2026-01-19
First posted
2025-07-15
Last updated
2026-01-29

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT07066345. Inclusion in this directory is not an endorsement.