Can a Two-Hour class rewire how women feel chronic pelvic pain?

NCT ID NCT07812857

What the study statuses mean

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Recruitment status, easiest to join first

Recruiting now
This trial is taking on new participants right now.
Not yet recruiting This study
Registered, but not yet taking participants.
By invitation only
Not open to general applications. Only people the study team invites can take part.
Paused
Paused for now. It may or may not start again.
Ongoing
Running, but no longer taking on new participants.
Completed
The trial has finished. Results may not be published yet.
Stopped early
Stopped early, before it reached the end. That can be for many reasons, including safety.
Cancelled
Cancelled before anyone took part.

Expanded access (not trials)

Expanded access
Not a trial. This treatment can be requested outside a study, case by case, for people who qualify.
Expanded access (paused)
Not a trial. The treatment can normally be requested outside a study, but is unavailable right now.
Expanded access (ended)
Not a trial. The treatment could once be requested outside a study, but no longer can.
Approved
The treatment has been approved, so it is available normally rather than through this programme.

When the status isn't known

Details not published
The full record has not been published yet, so there is little to show here.
Status unknown
This status has not been confirmed recently, so it may be out of date.

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

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

About 100 people

The number the study aims to enrol. It can still change while the study runs.

Expected to start

Oct 2026

An estimate. Start dates often move.

Expected to finish

Dec 2027

An estimate. End dates often move.

Lead sponsor

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

18 to 70 years

Sex

Female participants only

Healthy volunteers

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

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

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  2. The official record

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Contacts and locations

Locations

  • University of Chicago

    Chicago, Illinois, 60637, United States

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