Den här översättningen är inte klar ännu. Den här sidan är just nu på engelska.

Gå till den engelska sidan

Cure My Disease

Don't miss your cure!

 Log in / Sign up

Which training helps new moms most? study compares two approaches

NCT ID NCT06422780

Knowledge-focused Sponsor: Çankırı Karatekin 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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 24, 2026 · Last updated Jun 26, 2026 · Updated 1 time

Summary

This completed trial compared two training programs for first-time pregnant women: one focused on preparing for the maternal role, and the other on mindfulness-centered occupational therapy. The study included 74 women between 14-27 weeks of pregnancy and followed them after birth. The goal was to see which program better improves health awareness and maternal readiness.

What this could mean

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

Active substance
Maternal Role Preparation Training and Awareness-Centred Occupational Therapy Training
What this could lead to
If successful, this could point toward better ways to support first-time mothers during pregnancy and after birth.
What could go wrong
This is a small, completed trial with 74 participants, so results may not apply to all pregnant women. The outcomes are based on questionnaires, not hard medical endpoints.

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

74 people

The number who actually took part.

Started

May 2024

Finished

May 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 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 for pregnant women: * 18 to 35 years of age * Having conceived naturally * Being between 14-27 weeks of gestation * To be literate * Being primiparous * Reading and understanding Turkish * Volunteering to participate in the study * To have attended 80% of the trainings given Inclusion criteria for women in the postpartum period: * Giving birth at term * Having a healthy newborn (newborn born at 38-42 weeks of gestation, without low birth weight, without any disease) * Providing active care to the newborn baby with or without assistance Exclusion criteria for pregnant women * Having a risky pregnancy (gestational diabetes, eclampsia, pre-eclampsia, threatened preterm birth, premature rupture of membranes, placental anomalies etc.) * Having a maternal physical anomaly * Communication difficulties and mental deficiency * Having a medical history of mental illness * Having a foetal abnormality during pregnancy * Having a disease/complication that developed during pregnancy Exclusion criteria for women in the postpartum period: * Experiencing a traumatic event within 6-8 weeks postpartum (loss/death of a close person, natural disasters, accident, assault) * Stillbirth or having a baby with anomalies * Having a baby that requires an intensive care environment in a hospital * Mothers diagnosed with psychiatric illness (schizophrenia, depression, anxiety, panic attacks)

Get updates

Get notified about this study

Sign up to get updates when this study changes or when new studies for Postpartum complication are added.

Vår säkerhetsrekommendation!

Genom att skicka in godkänner du våra Användarvillkor

Conditions

The condition(s) this trial relates to.

pregnancy disorder puerperal disorder

As listed by the trial registrant

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

Postpartum complication Pregnancy related

Contacts and locations

Locations

  • Çankırı Karatekin University Occupational Therapy Department

    Çankırı, Çankırı, 18100, Turkey (Türkiye)

More trials for these conditions

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