Can training hospital staff in Trauma-Informed care make childbirth safer?

NCT ID NCT07823361

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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 Sep 16, 2026 · Last updated Sep 17, 2026 · Updated 1 time

Summary

Researchers at a state hospital in Turkey are testing whether training an entire maternity unit in trauma-informed care changes the experience of childbirth. The program teaches hospital leaders, midwives, nurses, doctors, and support staff to communicate respectfully, protect women's dignity, and avoid re-traumatizing patients. The study follows women giving birth at the hospital and the professionals who care for them, measuring birth-related post-traumatic stress symptoms and staff trauma-related stress. The goal is to see whether an organization-wide approach can improve psychological safety in maternity services.

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 care training for maternity hospital staff
What this could lead to
If it works, this could give hospitals a practical model for making maternity care feel safer and reducing trauma for women and the staff who care for them.
What could go wrong
Training alone may not change deep-rooted hospital routines or improve women's experiences. The study measures symptoms and staff stress, so it may not capture every part of care quality.

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 345 people

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

Expected to start

Sep 2026

An estimate. Start dates often move.

Expected to finish

May 2028

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 years and older

Sex

Anyone

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: Women: * Aged 18 years or older. * Giving birth at Tarsus State Hospital during the study period. * Providing voluntary informed consent. Healthcare professionals, organizational leaders, and support staff: * Aged 18 years or older. * Working in maternity or related services at Tarsus State Hospital. * Participating in the trauma-informed care intervention according to their professional role. * Providing voluntary informed consent. Exclusion Criteria: Women: * Severe postpartum complications preventing participation or completion of study assessments. * Incomplete study assessments. Healthcare professionals, organizational leaders, and support staff: -Failure to complete the required training or study assessments. Incomplete study assessments.

Get updates

Get notified about this study

Sign up to get updates when this study changes or when new studies for Post-traumatic stress disorder are added.

Our safety recommendation!

By submitting, you agree to our Terms of use

Conditions

The condition(s) this trial relates to.

Birth Injuries post-traumatic stress disorder Psychological Trauma

As listed by the trial registrant

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

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

  • Tarsus State Hospital Tarsus, Mersin, Türkiye

    Mersin, Tarsus, 33400, Turkey (Türkiye)

More trials for these conditions

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