The effectiveness of a mobile app in reducing of post-traumatic stress symptoms

Completed

• Conditions: Post-traumatic stress symptoms, post-traumatic stress disorder (PTSD), trauma related symptomsPosttraumatische stress symptomen, posttraumatische stressstoornis (PTSS), trauma gerelateerde symptomen

• Registration Number: NL-OMON29192
• Lead Sponsor: Academic Medical Center (AMC), University of Amsterdam, Amsterdam

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Last Update Posted: 11 June 2024

Recruitment & Eligibility

• Status: Completed
• Sex: Not specified
• Target Recruitment: 276

Inclusion Criteria

This study is conducted with adults in a high risk profession (e.g., ambulance and emergency department personnel).

Exclusion Criteria

1. No smartphone or tablet

2. No informed consent

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
The difference in post-traumatic stress symptoms (continuous PCL-5 scores) between the intervention and control condition directly after termination of the intervention period.

Secondary Outcome Measures

Name	Time	Method
1. The difference in negative cognitions about the trauma (PTCI) between the intervention and control condititon directly after termination of the intervention period.<br /><br>2. The difference in psychological resilience (RES) and perceived social support (SSL-6) between the intervention and control condition directly after termination of the intervention period.<br /><br>3. User satisfaction with the SUPPORT Coach will be evaluated and user logs will be explored for implementation-information purposes.