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Note: This record shows only the 20 elements of the WHO Trial Registration Data Set. To view changes that have been made to the source record, or for additional information about this trial, click on the URL below to go to the source record in the primary register.
Register: Netherlands Trial Register
Last refreshed on: 27 May 2013
Main ID:  NTR831
Date of registration: 07/12/2006
Primary sponsor: University Maastricht (UM)
Public title: Prevention of Posttraumatic stress disorder in Children and Adolescents.
Scientific title: Prevention of Posttraumatic stress disorder in Children and Adolescents. - N/A
Date of first enrolment: 1/12/2006
Target sample size: 80
Recruitment status: complete
URL:  http://www.trialregister.nl/trialreg/admin/rctview.asp?TC=831
Study type:  intervention
Study design:  Randomised: Yes; Masking: Single; Control: Not applicable; Group: Crossover; Type: [default]  
Countries of recruitment
The Netherlands
Contacts
Name: Manon J.B.  Vincken
Address:  University Maastricht, Department of Medical, Clinical and Experimental Psychology, P.O. Box 616 6200 MD Maastricht The Netherlands
Telephone: +31 (0)43 3881047
Email: m.vincken@dmkep.unimaas.nl
Affiliation: 
Name: Iris M.  Engelhard
Address:  University Medical Center Utrecht (UMCU), Department of Clinical Psychology, P.O. Box 80140 3508 TC Utrecht The Netherlands
Telephone: +31 (0)30 2531542
Email: i.m.engelhard@fss.uu.nl
Affiliation: 
Key inclusion & exclusion criteria
Inclusion criteria: Children (aged 7-17) who have had contact with Victim Assistence experiencing a traumatic event less than 2 weeks ago, children meet the DSM-criteria for Acute Stress Disorder.
Exclusion criteria: Exclusion criteria include:

1. Brain injury;

2. Psychotic of organic mental dirorder;

3. Current suicidal ideation;

4. IQ less than 80;

5. Proficiency in Dutch;

6. No parent willing to participate in the study.


Age minimum:
Age maximum:
Gender:
Health Condition(s) or Problem(s) studied
Posttraumatic stress disorder (PTSD)

Intervention(s)
Brief trauma-focused cognitive behavioral intervention or control-condition (wait-list-controls).
Primary Outcome(s)
Presence vs. absence of Posttraumatic Stress Disorder, and PTSD-symptom-severity (assessed with structured interview (ADIS-C interview Anxiety disorders interview scedule for children) and self-completed questionnaires (CPSS: child posttraumatic stress scale)).
Secondary Outcome(s)
Symptomss of anxiety and/or depression according to questionnaires (a.o. RCADS: revised children's anxiety and depression scale) and quality of life.
Secondary ID(s)
ISRCTN07286192
N/A
Source(s) of Monetary Support
ZON-MW, The Netherlands Organization for Health Research and Development
Secondary Sponsor(s)
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