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WHO-Based care model aims to make childbirth less traumatic for First-Time moms

NCT ID NCT06691854

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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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

Summary

This study tested a special care model for labor and delivery, based on World Health Organization recommendations, to see if it improves how women feel about their birth experience. The study included 124 first-time mothers with a single, healthy baby. Researchers compared women who received this model to those who did not, using surveys to measure respectful care, birth experience, and traumatic birth perception.

What this could mean

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

Active substance
Intrapartum care model based on WHO recommendations
What this could lead to
If successful, this model could improve how women feel about their birth experience and reduce feelings of trauma during childbirth.
What could go wrong
This is a small, completed study with 124 participants, so results may not apply to all women or settings. The outcomes are based on surveys, which can be subjective.

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

124 people

The number who actually took part.

Started

Dec 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 to 45 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: * Those who are 18 years of age or older, * Those who are in term pregnancy (38-41 weeks), * Those who are primiparous, * Those who have a single, healthy, vertex positioned fetus, * Those who have cervical dilatation of 5 cm or more, * Those who can speak and understand Turkish, * Those who voluntarily agree to participate in the research. Exclusion Criteria: * Those with chronic diseases (hypertension, diabetes, etc.), * Those with a diagnosed mental illness (depression, anxiety or other psychotic disorder, etc.), * Those with maternal and fetal complications (oligohydramnios and polyhydramnios, placenta previa, preeclampsia, premature membrane rupture, presentation anomalies, intrauterine growth retardation, fetal anomalies, intrauterine death, macrosomic baby, cord prolapse, etc.), * Those with any complications that prevent vaginal birth (cephalopelvic disproportion, etc.), * Elective cesarean section, * Those who became pregnant with assisted reproductive techniques, * Those who received childbirth preparation training.

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Conditions

The condition(s) this trial relates to.

Birth Injuries

As listed by the trial registrant

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

Birth, first Intrapartum fetal distress Maternity Traumatic birth

Contacts and locations

Locations

  • Seyhan Çankaya

    Konya, Konya, 42250, Turkey (Türkiye)

More trials for these conditions

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