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Mindfulness app may ease endometriosis pain without pills

NCT ID NCT07501182

Symptom relief Sponsor: Unity Health Toronto Source: ClinicalTrials.gov ↗

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Cancelled before anyone took part.

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First seen Jun 27, 2026 · Last updated Jun 27, 2026

Summary

This study tests whether a 10-week virtual mindfulness program can improve quality of life for people with endometriosis-related chronic pelvic pain. Researchers will enroll 124 adults aged 18-50 with a diagnosis of endometriosis. Participants will attend online mindfulness workshops, and the team will measure pain and well-being using questionnaires.

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 124 people

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

Expected to start

Mar 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 50 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: 1\. Be between the ages of 18 and 50; 2. Have been symptomatic for six months or greater; 3. Clinical or surgical diagnosis of endometriosis (must have at least one of the following): i) Documented Clinical Diagnosis of endometriosis based on symptoms ii) Previous endometriosis surgery confirmed by histopathology iii) Imaging suggestive of endometriosis (ultrasound or MRI) iv) Receiving standard medical treatment for endometriosis including combined oral contraceptives, progestin, GnRH agonists, GnRH antagonist. Exclusion Criteria: 1. Diagnosis of other chronic pain condition, other than endometriosis; 2. Recent surgical cases (\< 6 months) 3. Vulvar pain diagnosis including vulvodynia, vaginismus 4. Changes to current medical treatment or surgical intervention for endometriosis during the workshop period (10 weeks) 5. Inability to complete the survey package 6. Currently practicing mindfulness meditation. 7. Have used the MyEndo phone application previously 8. No internet access 9. Non-English speaking. 10. Unable to consent.

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Conditions

The condition(s) this trial relates to.

Chronic Pain chronic pain syndrome endometriosis

As listed by the trial registrant

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

Chronic pain Endometriosis

How to take part

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  1. The official record

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