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.
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
None
Parallel
prevention algorithm
Other interventiona health watch adapted to stress and dissociative symptoms
Standard care
Other interventionStandard care for post traumatic stress disorder
study acceptability rate
Number of included patient divided by number of patients to whom the study was offered. Study acceptability rate of 50% is expected.
Adherence of patient to the watch
Number of patient contacted by phone having completed the scales divided by number of patient contacted.
Adherence of patient to the health watch
Number of patient contacted by phone having completed the scales divided by number of patient contacted
Patient satisfaction (quantitatif)
A questionnaire will be completed by the patient
Patient satisfaction (qualitatif)
semi-structured interview carried-out in 3 patients volunteers (45 minutes)
Click on the lead sponsor to view all of their trials.
This trial is not recruiting at the moment. You can still explore other options:
