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Coloring away the baby blues: mandala art tested for postpartum mental health

NCT ID NCT07312812

Symptom relief Sponsor: Afyonkarahisar Health Sciences University Source: ClinicalTrials.gov ↗

What the study statuses mean

This study's is highlighted.

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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 Jun 24, 2026 · Last updated Jun 27, 2026 · Updated 1 time

Summary

This study tests whether a simple art activity—coloring mandalas—can reduce anxiety and depression in new mothers. Sixty women who recently gave birth will be randomly assigned to either practice mandala coloring at home for eight weeks or receive standard postpartum care. Researchers will measure changes in mood using questionnaires to see if this low-cost, non-drug approach offers any mental health benefit.

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 activity
What this could lead to
If it works, this could offer a simple, low-cost way to help new mothers manage anxiety and depression after childbirth.
What could go wrong
This is a small, early-stage trial with only 60 participants. The results may not apply to all women, and the benefit may be small or no different from usual care.

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 60 people

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

Expected to start

Jan 2026

An estimate. Start dates often move.

Expected to finish

Apr 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: * Able to speak and understand Turkish * Voluntarily agree to participate in the study and have signed the informed consent form * 18 years of age or older * Literate * Have not received any psychiatric diagnosis and are not currently receiving psychological or psychiatric support (therapy, counseling, or medication treatment) * Have not experienced any complications during delivery * Have a newborn with no malformation or anomaly * Have a newborn with no complications Exclusion Criteria: * Have previously received psychological or psychiatric treatment or are receiving such treatment during the data collection period, * Have a serious neurological or psychiatric disorder that affects cognitive functioning, * Have serious health problems that prevent communication or participation in the study, * Have not provided informed consent, * Are unable to speak or understand Turkish, * Have experienced complications during delivery, * Have a newborn with a malformation or anomaly, * Have a newborn with any complications.

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Conditions

The condition(s) this trial relates to.

anxiety disorder Depression postpartum depression

As listed by the trial registrant

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

Postpartum anxiety Postpartum depression

How to take part

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

  1. 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 ↗

  2. 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.

More trials for these conditions

Other studies related to the condition(s) this trial covers.