Post-traumatic stress disorder following childbirth.
Deniz Ertan, Coraline Hingray, Elena Burlacu...
https://pubmed.ncbi.nlm.nih.gov/33726703Actively Recruiting
Phase Not Applicable
Age: 18Years - 65Years
FEMALE
ID07246356
A Study to Explore the Feasibility and Efficacy of Group Traumatic Episode Protocol (GTEP) for Reducing Trauma Symptoms Following a Traumatic Birthing Experience
Led by University of Birmingham · Updated on 2026-02-19
10
Participants Needed
1
Research Sites
N/A
Total Duration
On this page
AI-Summary
What this Trial Is About
This research aims to evaluate the feasibility and initial effectiveness of the Group Traumatic Episode Protocol (GTEP) in reducing trauma symptoms for individuals who have experienced a traumatic birthing experience. It also seeks to assess the impact of GTEP on improving parental wellbeing and parent-infant bonding. The study is conducted by the University of Birmingham and focuses on trauma symptoms measured by tools like the PCL-5 and City BiTS, along with wellbeing and bonding assessments. Participants will take part in an 8-session GTEP intervention delivered online. The program starts with a home visit to obtain consent, confirm eligibility, and complete initial outcome measures. This is followed by six weekly 90-minute online group therapy sessions via Zoom. The final session is a post-group follow-up conducted face-to-face or by phone to review experiences, complete final measures, and discuss any further referrals. During the study, participants will complete various questionnaires before, during, and after the intervention to track trauma symptoms, wellbeing, and bonding. Feedback on the group's acceptability and feasibility will also be gathered from both participants and facilitators. The entire process from enrollment to follow-up spans up to 24 weeks, with the primary outcome measured multiple times. Analysis includes both quantitative and qualitative methods to understand the intervention's impact and feasibility.
CONDITIONS
Brief Title
Feasibility and Efficacy of GTEP for Birth Trauma
Who Can Participate
Age: 18Years - 65Years
FEMALE
Eligibility Criteria
You may qualify if you...
- 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.
- Access to technology such as a laptop and internet to join the online group.
- Access to a confidential space at home and childcare for baby or other children.
- Proficient in English to engage with the group.
- Able to participate in group therapy based on clinical presentation.
- Capacity to consent to the group therapy and research study.
You will not qualify if you...
- Women or birthing people whose baby is no longer under their care.
- Severe and enduring mental health conditions such as bipolar disorder, psychosis, or schizophrenia.
- Significant sensory impairments requiring a British Sign Language interpreter.
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
1
2
3
Your Study Journey
Screening
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (home visit to gain consent, determine eligibility, and complete outcome measures)
Treatment
Duration - Approximately 8 weeks
Participants attend a total of 8 GTEP sessions to reduce trauma symptoms following a traumatic birthing experience, including preparation, processing, and follow-up.
1 home visit, 6 weekly online group sessions via Zoom, and 1 post-group follow-up visit (in-person or telephone)
Trial Site Locations
Total: 1 location
1
Black Country Healthcare NHS Foundation Trust
Wolverhampton, United Kingdom, WV4 5HN
Actively Recruiting
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Research Team
G
Grace E Rodgers, Study Chief Investigator
R
Rachel Strachan, Study Principal Investigator
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
NA
Model
SINGLE_GROUP
Primary Purpose
TREATMENT
Number of Arms
1
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