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Behavioral Intervention

Online Self-Management Program for Chronic Pelvic Pain

N/A
Recruiting
Led By Sara Till, MD
Research Sponsored by University of Michigan
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial
Must have
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 6 months
Awards & highlights
No Placebo-Only Group

Summary

This trial aims to see if an online self-management program can help patients with Chronic Pelvic Pain feel better. The researchers believe that patients using the program will have less pain, better physical function, and

Who is the study for?
This trial is for individuals experiencing chronic pelvic pain, which may include conditions like endometriosis. Participants should be seeking new ways to manage their pain and improve their quality of life.
What is being tested?
The study compares a standard control group website with the 'My Pelvic Plan' website, designed to help patients self-manage chronic pelvic pain through various strategies aiming at improving pain levels and daily functioning.
What are the potential side effects?
Since this intervention involves web-based information and self-management techniques without medications or invasive procedures, no direct side effects are expected from participating in this trial.

Timeline

Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~6 months
This trial's timeline: 3 weeks for screening, Varies for treatment, and 6 months for reporting.

Treatment Details

Study Objectives

Study objectives can provide a clearer picture of what you can expect from a treatment.
Secondary study objectives
PROMIS Self Efficacy for Managing Symptoms SF 4a between groups
PROMIS pain intensity 1a between groups
Patient Reported Outcomes Measurement Information System (PROMIS) Pain Interference short form (SF) 4a between groups

Awards & Highlights

No Placebo-Only Group
All patients enrolled in this study will receive some form of active treatment.

Trial Design

2Treatment groups
Experimental Treatment
Group I: My Pelvic Plan plus usual careExperimental Treatment1 Intervention
Participants will have access to My Pelvic Plan program.
Group II: Monitoring progress plus usual careExperimental Treatment1 Intervention
Participants will have access to the monitoring progress web-based symptom monitoring program.

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Who is running the clinical trial?

University of MichiganLead Sponsor
1,852 Previous Clinical Trials
6,432,615 Total Patients Enrolled
Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD)NIH
2,051 Previous Clinical Trials
2,731,419 Total Patients Enrolled
15 Trials studying Endometriosis
4,543 Patients Enrolled for Endometriosis
Sara Till, MDPrincipal InvestigatorUniversity of Michigan
1 Previous Clinical Trials
30 Total Patients Enrolled
~83 spots leftby Apr 2026
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