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New program aims to stop postpartum depression in disaster zones

NCT ID NCT07329270

Prevention Sponsor: Istanbul Bilgi 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
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 This study
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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 25, 2026 · Last updated Jun 27, 2026 · Updated 1 time

Summary

This study tested a trauma-informed program to prevent postpartum depression in women living in earthquake-affected regions of Türkiye. The program included education, emotional support, and coping skills, delivered by healthcare workers. 106 women took part, and the study measured changes in depressive symptoms and stress levels.

What this could mean

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

Active substance
Trauma-informed preventive intervention (behavioral program including psychoeducation, emotional support, coping skills, and social support facilitation)
What this could lead to
If effective, this program could offer a practical, low-cost way to prevent postpartum depression in women living in disaster-affected areas.
What could go wrong
This is a single, completed trial with 106 participants, so results may not apply broadly. The program's success depends on local healthcare delivery and may not work in other settings or disasters.

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

106 people

The number who actually took part.

Started

Nov 2024

Finished

Jul 2025

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 years and older

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: Postpartum women aged 18 years or older Having an infant younger than 60 days at the time of enrollment Living in earthquake-affected regions of Türkiye Receiving routine postpartum follow-up through primary health care services Able to communicate in Turkish Provided written informed consent Exclusion Criteria: History of a diagnosed psychiatric disorder prior to the current postpartum period Severe medical conditions requiring specialized care Cognitive impairment or any con

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Conditions

The condition(s) this trial relates to.

postpartum depression prevention target

As listed by the trial registrant

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

Postpartum depression (PPD)

Contacts and locations

Locations

  • Narlıca 2 No'lu Family Physician Center

    Hatay, Antakya, Turkey (Türkiye)

More trials for these conditions

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