Novel Web-based, Self-directed Intervention for Chronic Pelvic Pain

Status: Completed
Location: See location...
Intervention Type: Behavioral
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

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.

Eligibility
Participation Requirements
Sex: Female
Minimum Age: 18
Healthy Volunteers: f
View:

• 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)

Locations
United States
Michigan
University of Michigan
Ann Arbor
Time Frame
Start Date: 2024-06-20
Completion Date: 2025-04-28
Participants
Target number of participants: 69
Treatments
Other: Monitoring progress plus usual care
Participants will have access to the monitoring progress web-based symptom monitoring program.
Experimental: My Pelvic Plan plus usual care
Participants will have access to My Pelvic Plan program.
Related Therapeutic Areas
Sponsors
Leads: University of Michigan
Collaborators: Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD)

This content was sourced from clinicaltrials.gov