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Mind over menstrual pain: could a Four-Week online program ease PCOS symptoms?

NCT ID NCT07718217

Symptom relief Sponsor: Aydin Adnan Menderes University Source: ClinicalTrials.gov ↗

What the study statuses mean

This study's is highlighted.

Recruitment status, easiest to join first

Recruiting now This study
This trial is taking on new participants right now.
Not yet recruiting
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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 Jul 21, 2026 · Last updated Aug 21, 2026 · Updated 2 times

Summary

This study tests whether a four-week online mindfulness-based education program can help women with Polycystic Ovary Syndrome (PCOS) manage menstrual symptoms, lower stress, and improve quality of life. About 78 women with PCOS will be randomly assigned to either the program or routine care. Researchers will measure changes in symptoms, stress, and well-being using standard questionnaires.

What this could mean

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

Active substance
a four-week online mindfulness-based education program for PCOS
What this could lead to
If effective, this program could offer a low-cost, non-drug way for women with PCOS to better manage symptoms and reduce stress.
What could go wrong
This is a small, early-stage study with 78 participants, so results may not apply to all women with PCOS. The program's benefits may be modest or short-lived.

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 78 people

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

Started

Jul 2026

Expected to finish

Dec 2026

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 49 years

Sex

Female participants only

Healthy volunteers

Accepted

You do not need to have the condition being studied to take part.

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: * Self-identify as female. * Be of reproductive age (18-49 years). * Have a confirmed diagnosis of Polycystic Ovary Syndrome (PCOS) based on the Rotterdam criteria. * Be able to read, understand, and communicate in Turkish. * Have access to the internet and a device capable of participating in online education sessions. * Be willing to attend the four-week online education program and complete all study assessments. * Provide written informed consent before participation. Exclusion Criteria: * Currently pregnant or breastfeeding. * Having a severe psychiatric disorder or cognitive impairment that may interfere with participation. * Having a serious chronic medical condition that could affect study outcomes or prevent participation in the intervention. * Currently participating in another interventional research study. * Having previously received structured mindfulness training or participated in a mindfulness-based program during the study period. * Being unable to attend the online education sessions or complete the study assessments. * Declining or withdrawing informed consent at any stage of the study.

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Conditions

The condition(s) this trial relates to.

Dysmenorrhea polycystic ovary syndrome

As listed by the trial registrant

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

Menstrual symptoms Polycystic ovary syndrome (PCOS) Quality of life Stress

How to take part

Only the study team decides who joins. These are the ways to reach them.

  1. The places running it

    1 site. The list below names each one and where it is.

  2. The official record

    ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.

    Open the record ↗

  3. 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

  • Bursa Uludag University obstetrics and gynecology clinic

    RECRUITING

    Bursa, Turkey (Türkiye)

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