Psychotrauma Prevention Algorithm : Randomized, Controlled Pilot Study
- Conditions
- Psychological Trauma
- Interventions
- Other: prevention algorithmOther: Standard care
- Registration Number
- NCT06366191
- Lead Sponsor
- Centre Hospitalier Universitaire de la Réunion
- Brief Summary
A randomized pilot study which proposes to patients having suffered a traumatic event to have either only the standard care or the standard care associated with adaptated psychotrauma watch and prevention system.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- NOT_YET_RECRUITING
- Sex
- All
- Target Recruitment
- 40
- Person who the vital prognosis has or could have been committed or having felt a threat to his physical and/or psychological integrity
- After a potentially traumatic event dating from a minimum of 72 hours to a maximum of 1 week
- for which the CUMP or the psychotrauma regulation platform has been requested
- having lived or being a direct witness of the event
- knowing how to read and write
- affiliate or beneficiary of a social security scheme
- having signed a consent
Non-inclusion Criteria:
- guardianship or curatorship
- unable to receive phone calls
- unable to go to a place for consultation
Not provided
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Arm && Interventions
Group Intervention Description Prevention algorithm prevention algorithm Patient will have the current support for psychotrauma and psychotrauma prevention algorithm. Current support for psychotrauma Standard care Patient will have the current support for psychotrauma.
- Primary Outcome Measures
Name Time Method study acceptability rate 6 months after inclusion Number of included patient divided by number of patients to whom the study was offered.
Study acceptability rate of 50% is expected.
- Secondary Outcome Measures
Name Time Method Adherence of patient to the health watch 3 months after inclusion Number of patient contacted by phone having completed the scales divided by number of patient contacted
Adherence of patient to the watch 1 month after inclusion Number of patient contacted by phone having completed the scales divided by number of patient contacted.
Patient satisfaction (qualitatif) 3 months after inclusion semi-structured interview carried-out in 3 patients volunteers (45 minutes)
Evolution of the patient journey in experimental arm 3 months after inclusion number an percentage of patient who have changed watch
Strong points of the health watch 3 months after inclusion semi-structured interview carried-out in volunteer caregivers (doctor, nurse, psychologist)
Patient satisfaction (quantitatif) 3 months after inclusion A questionnaire will be completed by the patient
Occurrence of post-traumatic stress disorder 3 months after inclusion Evaluation by Posttraumatic Stress Disorder Checklist for DSM-5 (PCL-5). Score between 0 and 80. Score \< 38 : no post-traumatic stress disorder Score = or \> 38 : post-traumatic stress disorder
Complications associated with post-traumatic stress disorder 3 months after inclusion assessed by WHO Quality of life - Bref (WHOQOL Bref). This scale assessed 4 domains : physical health, mental health, social relations and the environment.
Overall Score is between 26 and 130. the higher the score, the better the quality of life