Clinical trial Recruiting at 1 site Interventional Ages 18 to 45 Women only

An 8-week mindfulness program to help new mothers remember and feel better about childbirth

Official title: The Effect of Mindfulness-Based Stress Reduction Program on Birth Memory and Perception of Traumatic Birth: A Randomized Controlled Trial

Run by Inonu University · NCT07018765 · Data updated 2026-11-12

This program will try an 8-week Mindfulness-Based Stress Reduction course to see if it improves birth memory and reduces feelings of traumatic birth in women after a vaginal delivery.

Quick facts

Study typeInterventional
Ages18 Years to 45 Years
SexWomen only
Enrollment80 (estimated)
SponsorInonu University
Academic / other
Locations1 site (Malatya, Leave Blank)
StatusRecruiting
StartedJanuary 1, 2026
Main results expectedJune 2026
Study endsDecember 2026
Registry record updatedApril 9, 2026
Trial IDNCT07018765 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Women who had a vaginal birth, are literate in Turkish, have no diagnosed psychiatric disorder, and have internet access and a smart device are ideal candidates.

Probably not a fit

Women with a history of pregnancy loss, stillbirth, neonatal death, postpartum complications, diagnosed psychiatric disorders, or those unable to attend sessions or complete data collection may not benefit.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This is a randomized controlled, pretest-posttest design enrolling 80 women who had vaginal deliveries at Malatya Training and Research Hospital between July and October 2025. Forty participants will take part in an 8-week MBSR program (first session face-to-face, remaining weekly sessions online, 60–90 minutes each) while 40 control participants receive no intervention. Outcomes are measured before and after the program using the Mindfulness Scale, the Birth Memory and Recall Scale, and the Traumatic Birth Perception Scale. Primary endpoints are changes in birth memory and traumatic birth perception scores, analyzed with t-tests and descriptive statistics.

Why it matters

Potential benefit: If successful, the program could reduce distressing birth memories and lower perceptions of traumatic birth, improving postpartum mental well-being.

How similar studies have gone: Similar mindfulness programs have shown promise in reducing postpartum stress and improving maternal mental health, though applying MBSR specifically to birth memory and traumatic birth perception is less extensively studied.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

* Women who have undergone a vaginal birth
* Literate and able to understand Turkish
* No diagnosed psychiatric disorder
* Have access to internet and a smart device (for online MBSR sessions)

Exclusion Criteria:

* History of pregnancy loss, stillbirth, or neonatal death
* Complications during postpartum period in mother or newborn
* Incomplete data collection or failure to attend MBSR sessions

Where it's running

  • Malatya Education and Research Hospital
    Malatya, Leave Blank, Turkey (Türkiye)
    Recruiting

Study contacts

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How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.