Can a Two-Hour class rewire how women feel chronic pelvic pain?
NCT ID NCT07812857
First seen Sep 10, 2026 · Last updated Sep 15, 2026 · Updated 3 times
Summary
Researchers at the University of Chicago are testing whether adding a single-session pain management class called Empowered Relief to standard care helps women with chronic pelvic pain more than standard care alone. The trial enrolls 100 women aged 18 to 70 who have had pelvic pain for at least six months and at least seven days a month. Participants attend a virtual class that teaches relaxation, reframing, and coping skills, and researchers measure changes in how much pain interferes with daily life, pain intensity, and quality of life.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Empowered Relief, a single-session behavioral pain management class
- What this could lead to
- If it works, this could give doctors a low-cost, single-class option to help women with chronic pelvic pain manage how much pain disrupts their daily lives.
- What could go wrong
- This is a small, single-center study of a behavioral class, so results may not hold up in larger or more diverse groups. Some participants may not find the techniques helpful, and the trial does not test whether the class changes the underlying cause of the pain.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
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Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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About 100 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
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Oct 2026
An estimate. Start dates often move.
- Expected to finish
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Dec 2027
An estimate. End dates often move.
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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18 to 70 years
- Sex
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Female participants only
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Participant is willing and able to provide written informed consent. * Has pelvic pain of at least 6 months in duration and at least 7 days per month; defined as pain in the abdomen below the level of the umbilicus, bladder pain, and/or vaginal pain. * Female sex at birth * Clinic pain intensity score of at least 4 (range, 0-10, with 10 indicating worst pain imaginable) * English fluency * Adults aged 18 to 70 years Exclusion Criteria: * Patients scheduled for surgery within the study period or within 1 month post-op * Gross cognitive impairment
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As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The places running it
1 site. The list below names each one and where it is.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Locations
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University of Chicago
Chicago, Illinois, 60637, United States
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