Malatya Education and Research Hospital
Malatya, Leave Blank, 440000, Turkey (Türkiye)
Location status: Recruiting
NCT Number: NCT07018765
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.
Interested in participating?
Request Info18 year–45 year
Female
Interventional
Not applicable
Malatya, Leave Blank, 440000, Turkey (Türkiye)
Location status: Recruiting
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.
Healthy volunteers accepted: Yes
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
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.
Time frame: 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.
Time frame: Baseline 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.
Time frame: Baseline and 8 weeks post-intervention
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.
Contact information is provided by the study sponsor or research team.
Kader ATABEY
Other
The Effect of Mindfulness-Based Stress Reduction Program on Birth Memory and Perception of Traumatic Birth: A Randomized Controlled Trial
Acronym: MBSR-BIRTH
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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