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Main
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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. |
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Register:
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Netherlands Trial Register |
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Last refreshed on:
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27 May 2013 |
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Main ID: |
NTR831 |
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Date of registration:
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07/12/2006 |
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Primary sponsor: |
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Public title:
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Prevention of Posttraumatic stress disorder in Children and Adolescents.
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Scientific title:
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Prevention of Posttraumatic stress disorder in Children and Adolescents. - N/A |
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Date of first enrolment:
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1/12/2006 |
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Target sample size:
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80 |
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Recruitment status: |
complete |
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URL:
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http://www.trialregister.nl/trialreg/admin/rctview.asp?TC=831 |
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Study type:
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intervention |
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Study design:
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Randomised: Yes; Masking: Single; Control: Not applicable; Group: Crossover; Type: [default]
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Countries of recruitment
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The Netherlands
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Contacts
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Name:
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Manon J.B.
Vincken |
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Address:
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University Maastricht, Department of Medical, Clinical and Experimental Psychology,
P.O. Box 616
6200 MD
Maastricht
The Netherlands |
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Telephone:
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+31 (0)43 3881047 |
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Email:
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m.vincken@dmkep.unimaas.nl |
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Affiliation:
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Name:
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Iris M.
Engelhard |
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Address:
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University Medical Center Utrecht (UMCU), Department of Clinical Psychology,
P.O. Box 80140
3508 TC
Utrecht
The Netherlands |
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Telephone:
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+31 (0)30 2531542 |
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Email:
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i.m.engelhard@fss.uu.nl |
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Affiliation:
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Key inclusion & exclusion criteria
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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:
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Health Condition(s) or Problem(s) studied
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Posttraumatic stress disorder (PTSD)
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Intervention(s)
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Brief trauma-focused cognitive behavioral intervention or control-condition (wait-list-controls).
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Primary Outcome(s)
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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)).
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Secondary Outcome(s)
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Symptomss of anxiety and/or depression according to questionnaires (a.o. RCADS: revised children's anxiety and depression scale) and quality of life.
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Secondary ID(s)
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ISRCTN07286192
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N/A
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Source(s) of Monetary Support
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ZON-MW, The Netherlands Organization for Health Research and Development
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