Track this trial free. DataLookout checks ClinicalTrials.gov daily and emails you which fields changed on NCT07246356 (status, enrollment, completion dates, endpoints, sites) when this record is updated. Free accounts track up to 5 trials.

Track this trial

Feasibility and Efficacy of GTEP for Birth Trauma

StatusRecruiting
PhaseNot applicable
Started
View on ClinicalTrials.gov ↗
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.

Record History

See every version on ClinicalTrials.gov ↗

  1. Primary and study completion dates: Mar 31, 2026 to Jun 30, 2026v2 Show 4 more changesShow less
    • Secondary endpoints: details revised at 3 of 6 entries
    • Study description expanded, about 95 words
    • Collaborators shortened, about 6 words
    • Eligibility criteria shortened, about 2 words
  2. Study First Submitted
  • Stopped: an ongoing trial was terminated, suspended or withdrawn.
  • Notable: the trial’s plan changed such as a big move in its timeline or size, a new primary endpoint, sponsor or phase, or recruiting opened or resumed.
  • Minor: routine progress and housekeeping, such as sites added or enrollment closed.
University of Birmingham
44 trials monitored
See 3 trials at risk
PTSD
889 trials monitored
See 54 trials at risk
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.
Trial Details
NCT Number NCT07246356
Lead Sponsor University of Birmingham
Conditions
(from sponsor)		 PTSD (Childbirth-Related), Psychological Wellbeing, Bonding
Related terms Birth Injuries, Stress Disorders, Post-Traumatic
Enrollment 10 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov