ClinicalTrials.gg
RecruitingNCT07018765MBSR-BIRTHUpdated Apr 9, 2026

Effect of Mindfulness-Based Stress Reduction on Birth Memory and Perception of Traumatic Birth

An interventional study of Mindfulness-Based Stress Reduction (MBSR) in Postpartum Psychological Stress, Mindfulness-Based Stress Reduction and Maternal Health, sponsored by Kader ATABEY. Recruiting at 1 site in Turkey (Türkiye). Open to female participants aged 18 Years to 45 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2026-04-09.

Sponsored by Kader ATABEY · Not applicable, Interventional, and Treatment

From the registry’s dates

  • Primary completion was expected by Jun 2026, 5 months ago, but the record still lists the study as recruiting.
  • Started Jan 2026; still recruiting 10 months later.
Phase
Not applicable
Study type
Interventional
Enrollment
80
Allocation
Randomized
Ages
18 Years to 45 Years
Sex
Female
01

Study summary

This randomized controlled trial aims to evaluate the effects of a Mindfulness-Based Stress Reduction (MBSR) program on birth memory and perception of traumatic birth among women who have undergone vaginal delivery. The study will be conducted between July and October 2025 at Malatya Training and Research Hospital. Participants in the intervention group will attend an 8-week MBSR program, while the control group will receive no intervention. Data will be collected using validated scales before and after the intervention. The primary outcomes are changes in birth memory and traumatic birth perception scores.

Read the detailed description

This study is a pretest-posttest control group experimental design conducted to determine the effects of a Mindfulness-Based Stress Reduction (MBSR) program on birth memory and the perception of traumatic birth. The population of the study will consist of women who have had a vaginal delivery and received postpartum care at Malatya Training and Research Hospital between July and October 2025. The sample will include 80 women, with 40 in the experimental group and 40 in the control group. The intervention group will participate in an 8-week MBSR program, which includes weekly 60-90 minute sessions-first face-to-face and the rest conducted online. The program content will cover mindful breathing, body awareness, stress and emotion regulation, and interpersonal mindfulness.

Data will be collected using the Mindfulness Scale, the Birth Memory and Recall Scale, and the Traumatic Birth Perception Scale. Pre-test data will be collected during the initial hospital visit, and post-test data will be collected at the end of the 8-week program. No intervention will be applied to the control group. Statistical analyses will include descriptive statistics, independent samples t-tests, and paired samples t-tests. Ethical approval has been applied for and informed consent will be obtained from all participants.

02

Conditions studied

  • Postpartum Psychological Stress
  • Mindfulness-Based Stress Reduction
  • Maternal Health
  • Traumatic Birth

Browse trials for

Keywords

  • Mindfulness
  • Postpartum Stress
  • Maternal Mental Health
  • Midwifery
03

In context

Birth Injuries

33 studies on the registry are indexed under Birth Injuries; 7 are open to participants now.

This study's planned enrollment of 80 is below the median of 115 across 24 interventional studies indexed under Birth Injuries.

Browse Birth Injuries studies →

Lead sponsor

This is the only study on the registry with Kader ATABEY as lead sponsor.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years to 45 Years
Sexes eligible
Female
Accepts healthy volunteers
Yes

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

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

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
05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
None (open label)
Enrollment
80 participants (estimated)

Study arms

  • Experimental
    MBSR Group

    Participants in this group will receive an 8-week Mindfulness-Based Stress Reduction (MBSR) program, including weekly 60-90 minute sessions covering mindful breathing, body awareness, emotion regulation, and stress management. The first session will be face-to-face, and subsequent sessions will be delivered online (Zoom).

    Behavioral: Mindfulness-Based Stress Reduction (MBSR)

  • No intervention
    Control Group

    Participants in this group will receive routine postpartum care and no additional intervention.

Interventions

  • BehavioralMindfulness-Based Stress Reduction (MBSR)

    The MBSR program consists of eight weekly sessions, each lasting 60-90 minutes. The first session will be delivered face-to-face in the hospital, and the remaining sessions will be conducted online via Zoom. The program content includes mindful breathing, body scanning, stress management, emotional regulation, and interpersonal mindfulness exercises.

06

What researchers measure

Primary outcomes

  1. Change in Birth Memory Score

    Assessed by the Birth Memory and Recall Scale. Measures the quality and nature of the memory related to the childbirth experience.Assessed by the Birth Memory and Recall Scale (range 6-147). Higher scores indicate more vivid, intense, and emotionally charged birth memories. Items are rated on a 7-point Likert scale. Items 1, 3, and 11 are reverse scored.

    Time frame: Baseline and 8 weeks post-intervention

Secondary outcomes

  1. Change in Perception of Traumatic Birth

    Measured using the Traumatic Birth Perception Scale to evaluate psychological responses and perceived trauma related to childbirth.Measured using the Traumatic Birth Perception Scale (range 0-130). Each item is scored from 0 to 10. Higher scores indicate a higher level of perceived trauma related to childbirth.

    Time frame: Baseline and 8 weeks post-intervention

Other outcomes

  1. Change in Mindfulness Level

    Assessed by the State Mindfulness Scale (range 21-105). Each item is scored from 1 to 5. Higher scores reflect greater mindfulness during the present moment.Assessed by the State Mindfulness Scale (range 21-105). Each item is scored from 1 to 5. Higher scores reflect greater mindfulness during the present moment.

    Time frame: Baseline and 8 weeks post-intervention

07

Study locations

1 of 1 sites recruiting
08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Timeline

Tracking since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reachedSimilar studies: half by the dot; the band is the middle halfHalf of similar studies reached it by the dot; the band is the middle half, from a quarter to three quarters

Started Jan 2026 (actual). Primary completion is estimated for Jun 2026, 5 months after the start.

Of 15 interventional studies with no phase under Birth Injuries, half reached primary completion within 7 months of starting (the median), counting those still running; a quarter within 4 and three quarters within 10. This study's planned 5 months is below that.

How these figures are worked out, and which studies are left out of them.

Registered
Jun 4, 2025
First posted
Jun 12, 2025
StartActual
Jan 1, 2026
Primary completionEst.
Jun 2026
CompletionEst.
Dec 2026
Last update
Apr 9, 2026
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
No changes since tracking began. The registry record was last updated on Apr 9, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT07018765
Lead sponsor
Kader ATABEY
Collaborators
Malatya Egitim Ve Arastirma Hastanesi
Responsible party
Kader ATABEY (Assistant Research, Faculty of Health Sciences, Inonu University, Inonu University) — Sponsor-investigator
First posted
Jun 12, 2025
Start date
Jan 1, 2026
Primary completion
Jun 2026 (estimated)
Completion
Dec 2026 (estimated)
Last update
Apr 9, 2026

Study contacts

KADER ATABEY
Contact
kader.atabey@inonu.edu.tr
05354682883

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Interested in this study?

Eligibility is decided by the study team. Share this record with your doctor or contact the team directly.

Contact study team

Follow this study

Get an email when the registry record changes — status, dates, results — or when someone posts here.

Sign in to follow

Discussion

Questions and observations about this study, from anyone following it. Not medical advice, and not a channel to the study team — their contact details are on the registry record.

Sign in to join the discussion. Reading takes no account; posting does. You choose a display name, and a pseudonym is the default.

Nothing here yet. If you are running this trial, taking part in it, or weighing whether to, this is the place to say so.

Start the discussion