Validating and realising a clinically tested A-EMDR application for postpartum traumas

Phase 2

• Conditions: (1) postpartum trauma; (2) negative or traumatic feelings after childbirth; 10010273; 10037176

• Registration Number: NL-OMON56920
• Lead Sponsor: Radboud Universitair Medisch Centrum

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Last Update Posted: 19 August 2024

Recruitment & Eligibility

• Status: Pending
• Sex: Not specified
• Target Recruitment: 20

Inclusion Criteria

Women (>= 18 yrs.) who have recently given birth at the Radboudumc, with
negative or traumatic childbirth experience at follow up (+- 6 weeks
postpartum)

Exclusion Criteria

Current or past psychotic disorder

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
<p>Structured interviews and questionnaires will be conducted to collect<br /><br>qualitative data on the feasibility of the intervention, including insights<br /><br>into the process, advantages and disadvantages, and patients' experiences of<br /><br>the application.</p><br>

Secondary Outcome Measures

Name	Time	Method
<p>Additional questionnaires are administered on comorbid symptoms (depressive<br /><br>symptoms (IDS) and anxiety symptoms (STAI), general functioning (OQ-45), and<br /><br>quality of life (WHODAS). This will allow us to investigate whether specific<br /><br>subgroups may influence feasibility and whether these scores change clinically.<br /><br>Furthermore, the trial will examine the extent to which traumatic events evoke<br /><br>no or significantly reduced emotional reactions in the patient, as measured by<br /><br>the PTSD Checklist (PCL-5), allowing for a conservative assessment of efficacy. </p><br>