Feasibility and Efficacy of GTEP for Birth Trauma
Recruiting
N/A
Interventional Study
PTSD (Childbirth-Related)
Psychological Wellbeing
Bonding
No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
At a Glance
- Age
- 18 – 65
- Sex
- Female
- Study type
- Interventional
- Purpose
- Treatment
- Participants needed
- 10 (estimated)
- Sponsor
- University of Birmingham · Other
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About This Trial
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 throug…
Trial Locations
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Eligibility Criteria
Inclusion Criteria:
* Aged between 18-65 years.
* Currently under the Black Country Perinatal Mental Health Service
* Experiencing self-reported trauma symptoms related to a birthing experience within the last 18 months (this includes the birth itself, the postnatal hospital stay, and/or any neonat…
Contacts