A Study to Explore the Feasibility and Efficacy of Group Traumatic Episode Protocol (GTEP) for Reducing Trauma Symptoms Following a Traumatic Birthing Experience

Status: Recruiting
Location: See location...
Intervention Type: Behavioral
Study Type: Interventional
Study Phase: Not Applicable
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.

Eligibility
Participation Requirements
Sex: Female
Minimum Age: 18
Maximum Age: 65
Healthy Volunteers: f
View:

• 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 neonatal admissions).

• Access to technology (e.g., laptop, internet connection) to be able to access the online group.

• Access to a confidential space within their home, and childcare for their baby/any other existing children.

• Proficient levels of English Language to engage with the group.

• Ability to engage in group therapy based on clinical presentation.

• Capacity to consent to engage in the GTEP group and research study.

Locations
Other Locations
United Kingdom
Black Country Healthcare NHS Foundation Trust
RECRUITING
Wolverhampton
Contact Information
Primary
Grace E Rodgers, Study Chief Investigator
gxr327@student.bham.ac.uk
Backup
Rachel Strachan, Study Principal Investigator
rachel.strachan1@nhs.net
Time Frame
Start Date: 2025-06-19
Estimated Completion Date: 2026-03-31
Participants
Target number of participants: 10
Treatments
Experimental: GTEP
Participants will receive the GTEP intervention, delivered online.
Related Therapeutic Areas
Sponsors
Leads: University of Birmingham
Collaborators: Black Country Healthcare NHS Foundation Trust

This content was sourced from clinicaltrials.gov