Coloring your way to calm: mandala art may soothe PMS anxiety and sleep woes

NCT ID NCT07785622

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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 Results may not be published yet.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

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Status unknown
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First seen Aug 25, 2026 · Last updated Aug 26, 2026 · Updated 1 time

Summary

This trial tests whether coloring mandalas—intricate circular patterns—can help reduce anxiety and improve sleep quality in female students who experience premenstrual syndrome (PMS). Participants will be asked to color mandalas, and researchers will measure changes in their anxiety levels and sleep quality using standard questionnaires. The goal is to see if this simple, non-pharmacological activity can be a helpful tool for managing PMS-related symptoms.

What this could mean

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

Active substance
Mandala coloring
What this could lead to
If effective, mandala coloring could offer a simple, accessible, non-drug way to help women manage anxiety and sleep problems linked to PMS.
What could go wrong
This is a small, early-stage trial, and results may not apply to all women. The effect may be modest, and individual responses can vary.

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 80 people

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

Expected to start

Nov 2026

An estimate. Start dates often move.

Expected to finish

Jun 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 25 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: * Female students aged 18 and older * Scoring 45 or higher on the Premenstrual Syndrome Scale * Scoring 36 or higher on the State-Trait Anxiety Inventory (STAI) * Scoring 5 or higher on the Pittsburgh Sleep Quality Index (PSQI) * Having a regular menstrual cycle (21-35 days) * Volunteering to participate in the study * Fully completing the survey and scale forms Exclusion Criteria: * Not wishing to continue participating in the study * Having any condition that hinders communication (such as impairments in hearing, speech, or comprehension) * Having a gynecological condition (e.g., abnormal uterine bleeding, uterine fibroids, ovarian cysts, undergoing hormonal therapy) * Having a chronic or physical illness * Having a psychological disorder * Undergoing psychiatric treatment (pharmacotherapy or psychotherapy) * Using pharmacological or non-pharmacological methods to alleviate premenstrual symptoms (e.g., oral contraceptives, acupressure, homeopathy, yoga) * Having a sleep-related issue and receiving treatment for it * Individuals who exercise regularly

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Conditions

The condition(s) this trial relates to.

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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  1. The places running it

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  2. The official record

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Contacts and locations

Locations

  • Kırklareli University

    Kırklareli, Turkey (Türkiye)

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