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Can a single day of online therapy ease postpartum depression?

NCT ID NCT07267702

Symptom relief Sponsor: Marmara 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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 27, 2026 · Last updated Jun 27, 2026

Summary

This pilot study tests whether a one-day online cognitive behavioral therapy (CBT) workshop can help women with postpartum depression in Türkiye. Sixty mothers with depressive symptoms will be randomly assigned to either the workshop or usual care. The study focuses on whether the approach is feasible and acceptable, and will measure changes in depression, anxiety, and thinking patterns after three months.

What this could mean

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

Active substance
One-day online cognitive behavioral therapy (CBT) group workshop
What this could lead to
If it works, this could offer a practical, low-cost way to reduce postpartum depression symptoms for new mothers in Türkiye.
What could go wrong
This is a small pilot study with only 60 participants, so results may not apply widely. It tests feasibility, not yet proven effectiveness.

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

Dec 2025

An estimate. Start dates often move.

Expected to finish

Jul 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 45 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: * Female participants aged 18-45 years * Having an infant aged 1-12 months * Presence of clinically relevant postpartum depressive symptoms (EPDS ≥10) * Literate in Turkish (able to read and write) * Access to a stable internet connection * Willing and able to provide informed consent Exclusion Criteria: * Current psychotic, bipolar, organic mental, or substance use disorder * Severe depressive episode or impaired judgment due to psychiatric illness * Active suicidal ideation or intent * Medical or neurological condition preventing participation (e.g., dementia, intellectual disability, severe hearing or visual impairment) * Infant with a life-threatening congenital disorder

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Conditions

The condition(s) this trial relates to.

Coitus depressive disorder mood disorder Motor Activity postpartum depression Psychological Well-Being

As listed by the trial registrant

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

Postpartum depression

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

  • Marmara University, Department of Psychiatry

    Istanbul, Marmara, 34854, Turkey (Türkiye)

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