Effect of Mindfulness-Based Stress Reduction on Birth Memory and Perception of Traumatic Birth
Condition(s) studied
Investigational drug(s) / intervention(s)
Mindfulness-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.
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.
Eligibility
Primary outcome measure(s)
- Change in Birth Memory Score — Baseline 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.
Trial sites (1)
| Facility | City | Region | Status |
|---|---|---|---|
| Malatya Education and Research Hospital | Malatya | Leave Blank | Recruiting |
Other trials for the same condition
This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.
View NCT07018765 on ClinicalTrials.gov ↗ ← All trials in Turkey