MedPath

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

Not Applicable
Not yet recruiting
Conditions
Postpartum Psychological Stress
Traumatic Birth
Mindfulness-Based Stress Reduction
Maternal Health
Registration Number
NCT07018765
Lead Sponsor
Kader ATABEY
Brief 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.

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.

Recruitment & Eligibility

Status
NOT_YET_RECRUITING
Sex
Female
Target Recruitment
80
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

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Primary Outcome Measures
NameTimeMethod
Change in Birth Memory ScoreBaseline and 8 weeks post-intervention

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.

Secondary Outcome Measures
NameTimeMethod
Change in Perception of Traumatic BirthBaseline and 8 weeks post-intervention

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.

Trial Locations

Locations (1)

Malatya Education and Research Hospital

🇹🇷

Malatya, Leave Blank, Turkey

Malatya Education and Research Hospital
🇹🇷Malatya, Leave Blank, Turkey

MedPath

Empowering clinical research with data-driven insights and AI-powered tools.

© 2025 MedPath, Inc. All rights reserved.