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Clinical Trials/ACTRN12615000438550
ACTRN12615000438550
Recruiting
未知

Randomised Controlled Trial of Enhanced Monitoring or Treatment As Usual for Adults to Treat PosttraumaticStress Disorder Following Traumatic Injury

niversity of Sydney0 sites200 target enrollmentMay 7, 2015
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Overview

Phase
未知
Intervention
Not specified
Conditions
Not specified
Sponsor
niversity of Sydney
Enrollment
200
Status
Recruiting
Last Updated
6 years ago
OverviewInvestigatorsEligibility CriteriaOutcomesSimilar Trials

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
May 7, 2015
End Date
TBD
Last Updated
6 years ago
Study Type
Interventional
Sex
All

Investigators

Eligibility Criteria

Inclusion Criteria

  • •Adults survivors of traumatic injury who are admitted to hospital following injury

Exclusion Criteria

  • •1\.Patients with a moderate to severe traumatic brain injury as defined by
  • •a.A GCS score \< 12 – as per the Emergency Department (ED) assessment
  • •b.Ongoing Post Traumatic Amnesia (PTA) testing \> 72 hours
  • •c.NOTE: Refer to MTBI decision making tree (appendix) if there are other reasons for altered GCS or PTA score (e.g., intubation of patient)
  • •2\.Patients unable to understand the study procedures, consent, or willingly participate in the study protocol
  • •3\.Patients with moderate dementia or severe cognitive impairment
  • •4\.Patients with severe suicidal ideation (i.e., if the injury was the result of a suicide attempt, as defined by the electronic medical records at Royal North Shore Hospital).
  • •5\.Patients with psychosis (as defined by the electronic medical records at Royal North Shore Hospital).

Outcomes

Primary Outcomes

Not specified

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