- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT01200628
DEPITAC : Short Screening Scale for Psychotraumatic Disorders After Motor Vehicle Accident (DEPITAC)
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
Status
Intervention / Treatment
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
Enrollment (Actual)
Contacts and Locations
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
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Sampling Method
Study Population
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
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:
|
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
Sponsor
Investigators
- Principal Investigator: Olivier COTTENCIN, MD PhD, University Hospital, Lille
Publications and helpful links
Study record dates
Study Major Dates
Study Start
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Estimate)
Study Record Updates
Last Update Posted (Estimate)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
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.
Clinical Trials on Stress Disorders, Post-Traumatic
-
University of California, Los AngelesDefense Advanced Research Projects Agency; Defense Group, Inc.CompletedPost-traumatic Stress Disorder | Post-Traumatic Stress Disorder, ChronicUnited States
-
Weill Medical College of Cornell UniversityCompletedPost-traumatic Stress Disorder | Complex Post-Traumatic Stress DisorderUnited States
-
Oregon Health and Science UniversityNational Center for Complementary and Integrative Health (NCCIH); Oregon Clinical...CompletedPost-Traumatic Stress DisordersUnited States
-
US Department of Veterans AffairsEmory UniversityWithdrawnPost-Traumatic Stress Disorders
-
University of KonstanzGerman Research Foundation; NGO vivo e.V.; GTZ-German Technical Cooperation,... and other collaboratorsCompletedPost-Traumatic Stress DisordersSri Lanka
-
University Hospital, ToulouseCompletedPost-traumatic StressFrance
-
University of California, Los AngelesRecruitingPost-traumatic Stress Disorder | Post-Traumatic Stress Disorder in ChildrenUnited States
-
University of UtahEunice Kennedy Shriver National Institute of Child Health and Human Development...CompletedPost-Traumatic Stress Disorder in Children | Post-Traumatic Stress Disorder in AdolescenceUnited States
-
University Hospital, LilleNot yet recruiting
-
Steinn SteingrimssonRecruiting