ClinicalTrials.Veeva

Menu

Psychotrauma Prevention Algorithm : Randomized, Controlled Pilot Study (A2P)

C

Centre Hospitalier Universitaire de la Réunion

Status

Not yet enrolling

Conditions

Psychological Trauma

Treatments

Other: Standard care
Other: prevention algorithm

Study type

Interventional

Funder types

Other

Identifiers

NCT06366191
2023/CHU/08

Details and patient eligibility

About

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.

Enrollment

40 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion and exclusion criteria

Inclusion Criteria:

  • 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

Trial design

Primary purpose

Prevention

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

40 participants in 2 patient groups

Prevention algorithm
Experimental group
Description:
Patient will have the current support for psychotrauma and psychotrauma prevention algorithm.
Treatment:
Other: prevention algorithm
Current support for psychotrauma
Active Comparator group
Description:
Patient will have the current support for psychotrauma.
Treatment:
Other: Standard care

Trial contacts and locations

0

Loading...

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2026 Veeva Systems