Clinical Trial

Feasibility and Efficacy of GTEP for Birth Trauma

Recruiting
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Record status
This record was last updated February 19, 2026 (before its estimated June 30, 2026 completion). Its status may not reflect the trial's current state.
Summary
This clinical study aims to evaluate the feasibility and initial efficacy of Group Traumatic Episode Protocol (GTEP) for reducing trauma symptoms (measured by the PCL-5 and City BiTS) for individuals following a traumatic birthing experience. A secondary aim is to evaluate the efficacy of GTEP in improving parental wellbeing (measured through the CORE-10) and parent-infant bonding (measured through the PBQ) following a traumatic birthing experience. Participants (those who have experienced a traumatic birthing experience) will complete the GTEP intervention, delivered online. They will be asked to complete outcome measures and give feedback on their experience of the group.
Protocol Amendment History 1 amendment
This ClinicalTrials.gov record has been amended once since 2025-11-17.
Trial Details
NCT Number NCT07246356
Lead Sponsor University of Birmingham
Conditions PTSD (Childbirth-Related), Psychological Wellbeing, Bonding
Enrollment 10 participants
Start Date 2025-06-19
Primary Completion 2026-06-30 (estimated)
Study Completion 2026-06-30 (estimated)
Updated on ClinicalTrials.gov 2026-02-19