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ID
Source
Brief title
Health condition
Post-traumatic stress symptoms, post-traumatic stress disorder (PTSD), trauma related symptoms
Posttraumatische stress symptomen, posttraumatische stressstoornis (PTSS), trauma gerelateerde symptomen
Sponsors and support
Intervention
Outcome measures
Primary outcome
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
1. The difference in negative cognitions about the trauma (PTCI) between the intervention and control condititon directly after termination of the intervention period.
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.
3. User satisfaction with the SUPPORT Coach will be evaluated and user logs will be explored for implementation-information purposes.
Study objective
We hypothesize that usage of the SUPPORT Coach app will lead to a reduction of post-traumatic stress symptoms directly after usage of the app compared to participants that do not use the app.
Furthermore, we expect that usage of the SUPPORT Coach will decrease negative cognitions about the traumatic event(s) and increase psychological resilience and social support.
Study design
Primary outcome: PCL-5 scores directly upon termination of the 1-month intervention period
Secondary outcomes: PTCI, RES, and SSL-6 scores directly upon termination of the 1-month intervention period
A follow-up is scheduled at 1 month after termination of the 1-month intervention period
Intervention
Participants in the intervention condition will receive unlimited access (during one month) to 'The SUPPORT Coach', a mobile application designed to support individuals with post-traumatic stress symptoms. The app includes information on post-traumatic stress and professional care, exercises and tools to manage traumatic stress symptoms, a self-test to monitor symptoms over time, a seek support section and a calendar function.
Participants in the control group will not receive access to the SUPPORT Coach. Participants in both conditions have access to their own (mental) care if necessary.
A. Bakker
Meibergdreef 5
Amsterdam 1105 AZ
The Netherlands
+31 - 20 891 3552
a.bakker@amc.nl
A. Bakker
Meibergdreef 5
Amsterdam 1105 AZ
The Netherlands
+31 - 20 891 3552
a.bakker@amc.nl
Inclusion criteria
This study is conducted with adults in a high risk profession (e.g., ambulance and emergency department personnel).
1. Age 18 years and older
2. Capable to read and comprehend the Dutch language
Only participants with at least one symptom of post-traumatic stress, objectified by a PC-PTSD-5 score of 1 or higher related to a traumatic event, will be randomized into one of two study conditions.
Exclusion criteria
1. No smartphone or tablet
2. No informed consent
Design
Recruitment
Followed up by the following (possibly more current) registration
Other (possibly less up-to-date) registrations in this register
No registrations found.
In other registers
Register | ID |
---|---|
NTR-new | NL4961 |
NTR-old | NTR5065 |
CCMO | NL48552.018.14 |
OMON | NL-OMON41202 |