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Peer support program aims to tackle endometriosis pain

NCT ID NCT06549985

First seen Jan 09, 2026 · Last updated Jun 19, 2026 · Updated 17 times

Summary

This study tests whether an 8-week group program called PEEPS, which combines education and peer support, can reduce how much endometriosis pain interferes with daily life. Sixty women aged 18-48 with confirmed endometriosis and chronic pelvic pain will either join PEEPS plus usual care or just receive an educational handout. Researchers will compare pain interference, physical function, and quality of life over 12 months.

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This is a summary of the original study . Summaries may miss details or leave out important information. Before applying or accepting participation, make sure you have read and understood the full study. Curemydisease.com takes no responsibility whatsoever for anything missed, misunderstood, or acted upon as a result of our summary — we know it does not capture everything.

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Contacts and locations

Study contacts

  • Contact

    Phone: •••-•••-•••• Email: •••••@•••••

  • Contact

    Phone: •••-•••-•••• Email: •••••@•••••

Locations

  • WashU Medicine

    RECRUITING

    St Louis, Missouri, 63108, United States

    Contact Phone: •••-•••-•••• Email: •••••@•••••

    Contact

    Contact Phone: •••-•••-•••• Email: •••••@•••••

What this could mean

Our plain-language read of the trial. This is informational only — not medical advice or a prediction.

Active substance

group support program (PEEPS) with education and peer support

What this could lead to

If it works, this could offer a new, non-drug way to help people with endometriosis manage chronic pelvic pain and improve daily function.

What could go wrong

This is a small pilot study (60 people) testing a behavioral program, not a drug. Results may not apply to everyone, and the program requires in-person attendance, which may not suit all patients.

Conditions

The condition(s) this trial relates to.

endometriosis Pelvic Pain

As listed by the trial registrant

The condition terms exactly as the trial's registrant entered them.