NCT07018765 Effect of Mindfulness-Based Stress Reduction on Birth Memory and Perception of Traumatic Birth
| NCT ID | NCT07018765 |
| Status | Recruiting |
| Phase | — |
| Sponsor | Kader ATABEY |
| Condition | Postpartum Psychological Stress |
| Study Type | INTERVENTIONAL |
| Enrollment | 80 participants |
| Start Date | 2026-01-01 |
| Primary Completion | 2026-06 |
Eligibility & Interventions
Eligibility Fast-Check
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What to Expect as a Participant
You will actively receive the study intervention — which may be a drug, biologic, device, or procedure.
This trial targets 80 participants in total. It began in 2026-01-01 with a primary completion date of 2026-06.
⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.
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.
Eligibility 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
Contact & Investigator
Frequently Asked Questions
Who can join the NCT07018765 clinical trial?
This trial is open to female participants only, aged 18 Years or older, up to 45 Years, studying Postpartum Psychological Stress. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.
Is NCT07018765 currently recruiting?
Yes, NCT07018765 is actively recruiting participants. Contact the research team at kader.atabey@inonu.edu.tr for enrollment information.
Where is the NCT07018765 trial being conducted?
This trial is being conducted at Malatya, Turkey (Türkiye).
Who is sponsoring the NCT07018765 clinical trial?
NCT07018765 is sponsored by Kader ATABEY. The trial plans to enroll 80 participants.