DEPITAC : Short Screening Scale for Psychotraumatic Disorders After Motor Vehicle Accident (DEPITAC)

June 16, 2015 updated by: University Hospital, Lille

Construction and Validation of a Short Screening Scale for Psychotraumatic Disorders for Inpatients Hospitalized in Surgical Unit Following a Road Traffic Accident

Posttraumatic stress disorder (PTSD) is a serious and often chronic response to overwhelmingly stressful events as Road Traffic Accident. Moreover PTSD is associated with increased rates of medical morbidity, poor health-related quality of life, and functional impairment. PTSD is prevalent in primary care settings after road traffic accident, where approximately 25% of patients meet diagnostic criteria for the disorder. Despite the development of a number of efficacious behavioral and pharmacological treatments, only a minority of patients with PTSD receive mental health services. PTSD is frequently underrecognized and untreated in Emergency Department and Surgical Unit.

Then, early diagnosis and prevention of PTSD might help to identify patients with PTSD high risk and lead them to benefit of personalized cares. Nevertheless it is not possible (neither useful) to provide psychological cares for each road traffic accident victim.

This is the reason why we think that nurses can help to screen patients who need treatment for PTSD Hypothesis : Recognition of specific clinical or biological signs occurring during road traffic accident victim hospitalization in surgical unit could allow beginning specific treatment using consultation liaison psychiatry.

Early treatment could allow decreasing incidence of psychotraumatic disorders, increasing surgical functional efficacy and improve convalescence programs. The use of a specific questionnaire could help to screen this disorder.

We have created the DEPITAC scale : a short screening questionnaire with 10 items.

This study will be evaluated DEPITAC's 10-item screen for posttraumatic stress disorder (PTSD) for use in surgical or emergency department.

Study Overview

Detailed Description

We include 300 road traffic accident victims hospitalized in surgical department (less than 2 weeks). Patients are hospitalized in 5 different hospitals (3 in Lille, 1 in Douai, 1 in Paris). Patients will be evaluated by a short screening questionnaire (DEPITAC's 10 item screen). Patients will be evaluated by phone with a experimented psychologist (Minimal International Neuropsychiatric Interview DSM IV, PTSD Check List symptoms) at 6 weeks, 6 months and 1 year after the accident.

Purposes :

  • To evaluate DEPITAC's 10-item screen for posttraumatic stress disorder (PTSD) for use in surgical or emergency department.
  • To measure prognosis value of DEPITAC's 10 item screen on acute PTSD (PTSD Check List symptoms (PCLs) 6th week) and late PTSD (PTSD Check List symptoms (PCLs) 6 months and 1 year) or other psychiatric disorder (anxiety, depression or addictive disorder) (Minimal International Neuropsychiatric Interview MINI DSM IV at 6 months and 1 year).
  • To compare DEPITAC to Peritraumatic Distress Inventory (PDI) given a the same time.
  • To calculate DEPITAC's total score and correlate to the onset of a PTSD at 6 week, 6 months and 1 year.

Study Type

Observational

Enrollment (Actual)

274

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

      • Douai, France
        • General Hospital, Douai
      • Grenoble, France
        • University Hospital, Grenoble
      • Lille, France
        • Catholic University Hospital of Lille Saint Philibert
      • Lille, France
        • Catholic University Hospital of Lille Saint Vincent
      • Paris, France
        • Georges Pompidou European Hospital, Paris
    • North
      • Lille, North, France, 59037
        • University Hospital, Lille

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

16 years and older (Adult, Older Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Sampling Method

Non-Probability Sample

Study Population

We include 250 road traffic accident victim hospitalized in surgical department (less than 2 weeks). Patients are hospitalized in 5 different hospitals (3 in Lille, 1 in Douai, 1 in Paris).

Description

Inclusion Criteria:

  • Road traffic accident victims hospitalized in surgical department less than 2 weeks
  • Can be called by phone

Exclusion Criteria:

  • Patient with a coma for more than 15 minutes
  • Patient with a crania traumatism and with loss of consciousness over 15 minutes
  • Homeless

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Observational Models: Cohort
  • Time Perspectives: Prospective

Cohorts and Interventions

Group / Cohort
Intervention / Treatment
Road traffic accident victims
Cohort of patients hospitalized in surgical department after a motor vehicle accident less than 2 weeks
heteroevaluation scale by a nurse during hospitalization
Other Names:
  • early screening PTSD scale

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
DEPITAC's 10 item screen score
Time Frame: six months
total score of DEPITAC scale
six months

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Peritraumatic Distress Inventory (PDI) results
Time Frame: six months / one year
six months / one year
MINI DSM IV results
Time Frame: six months / one year
Minimal International Neuropsychiatric Interview DSM IV
six months / one year
PTSD Check List symptoms results
Time Frame: six months / one year
six months / one year

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Principal Investigator: Olivier COTTENCIN, MD PhD, University Hospital, Lille

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start

June 1, 2007

Primary Completion (Actual)

June 1, 2015

Study Completion (Actual)

June 1, 2015

Study Registration Dates

First Submitted

March 18, 2010

First Submitted That Met QC Criteria

September 10, 2010

First Posted (Estimate)

September 13, 2010

Study Record Updates

Last Update Posted (Estimate)

June 17, 2015

Last Update Submitted That Met QC Criteria

June 16, 2015

Last Verified

June 1, 2015

More Information

Terms related to this study

Other Study ID Numbers

  • 2006_0632
  • DGS 2006-0053 (Other Identifier: AFSSAPS)
  • PHRC 2006/R1904 (Other Identifier: DHOS)
  • 2006-A00180-51 (Other Identifier: ID-RCB number, ANSM)

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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