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A new care protocol aims to support pregnant women in disaster zones

NCT ID NCT07058766

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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 Jul 28, 2026 · Last updated Jul 29, 2026 · Updated 1 time

Summary

This trial tests whether a structured care protocol can improve the physical and psychological health of pregnant women living in an area hit by a major earthquake. The study includes 43 pregnant women who are earthquake survivors and compares those who receive the protocol with those who do not. Researchers will measure depression, trauma levels, and overall psychosocial health to see if the extra support makes a difference.

What this could mean

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

Active substance
a care protocol providing physical and psychosocial support to pregnant women after a disaster
What this could lead to
If effective, this protocol could offer a practical way to improve mental and physical health for pregnant women living in disaster-affected areas.
What could go wrong
This is a small, single-site trial with 43 participants, so results may not apply broadly. The intervention is behavioral and may not address all needs.

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

43 people

The number who actually took part.

Started

Mar 2025

Finished

Mar 2026

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

19 to 35 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: * Over the age of 18, * Positive (+) pregnancy, * Able to read and write Turkish and speak and understand Turkish, * No mental or psychological disorder that would cause difficulty in expressing oneself, * Not receiving a score between 20-27 (severe depression) on HSA-9, * No chronic disease or high-risk pregnancy diagnosis requiring hospitalization and follow-up, * Volunteer to participate in the study Exclusion Criteria: * Under 18 years of age, * Foreign nationals who cannot read or write Turkish and are inadequate in speaking or understanding Turkish, * Those with any mental or psychological disorder/diagnosis, * Those who score between 20-27 (severe depression) on HSA-9, * Those with a chronic disease or a diagnosis of high-risk pregnancy requiring hospitalization and follow-up, * Those who do not agree to participate in the study

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As listed by the trial registrant

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

Contacts and locations

Locations

  • Hatay Mustafa Kemal Üniversitesi

    Hatay, Turkey (Türkiye)

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