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Exploring Patient Treatment Preferences for Chronic Pelvic Pain: A Mixed Methods Study

University of Michigan logo

University of Michigan

Status

Completed

Conditions

Chronic Pelvic Pain

Treatments

Behavioral: My Pelvic Plan website

Study type

Interventional

Funder types

Other
NIH

Identifiers

NCT06540560
HUM00253781
1K23HD099283-01A1 (U.S. NIH Grant/Contract)

Details and patient eligibility

About

This research is studying what things change the way people think about treatment for chronic pelvic pain (CPP). The study team is also interested in whether a web-based educational and self-management program for chronic pelvic pain changes how people think about chronic pelvic pain treatments. The program contains several different self-guided modules that include cognitive and behavioral structuring, self-administration of acupressure, engaging in physical activity, and a brief introduction to pelvic floor physical therapy techniques.

The study hypothesis is that patients with CPP will report that prior treatment experiences and most trusted source of medical information will be associated with baseline perceptions of various CPP treatment modalities.

Enrollment

30 patients

Sex

Female

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Have chronic pelvic pain, defined as moderate to severe pelvic pain (based on protocol) for greater or equal to(≥) 6-month duration, and is non-cyclic, occurring for at least 14 days of each month.
  • Must be 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.
  • Access to internet via computer or smartphone
  • English-language proficiency (current version of the website is in English)
  • The study team will attempt to recruit a diverse group of patients, with attention to diversity in race, ethnicity, education level, rural vs urban locality, sexual orientation, and gender identification.

Exclusion criteria

  • Severe physical impairment precluding participating in internet-based program (for example, complete blindness or deafness)
  • 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).

Trial design

Primary purpose

Health Services Research

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

30 participants in 1 patient group

My Pelvic Plan
Experimental group
Description:
This is a web-based self-guided program.
Treatment:
Behavioral: My Pelvic Plan website

Trial documents
1

Trial contacts and locations

1

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Central trial contact

Jordyn Boggan; Sara Till, MD

Data sourced from clinicaltrials.gov

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