- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT01253993
Impaired Decision-making in Adolescents
Impaired Decision-making in Adolescents: A Vulnerability Factor for the Development of Substance Use and Abuse.
Study Overview
Status
Detailed Description
This study consists of two substudies with adolescents in the age of 14-21 years. The first study group consist of adolescents with DBD with (n=30) and without (n=30) substance use disorders. These adolescents are recruited from orthopsychiatric, forensic psychiatric, and judicial institutions.
The second study group consists of a) ex-patients of the Utrecht Coping Power Program (UCPP)who previously participated to a follow-up study, and b) ex-patients who were treated as a child at an outpatient clinic of the UMC Utrecht. These latter groups were taken together and subdivided into a group with (n=30) and without (n=30) substance use problems.
For both studies healthy controls (n=80) are recruited. The investigators will start with healthy controls from earlier studies, and those are extented and will serve as control group for both studies.
Study Type
Enrollment (Actual)
Contacts and Locations
Study Locations
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Utrecht, Netherlands, 3584 CX
- University Medical Center Utrecht
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Sampling Method
Study Population
Description
Inclusion Criteria:
- Having a DISC diagnosis DBD
Exclusion Criteria:
- Having the DISC diagnosis Schizophrenia
Study Plan
How is the study designed?
Design Details
- Observational Models: Case-Control
- Time Perspectives: Cross-Sectional
Collaborators and Investigators
Sponsor
Collaborators
Investigators
- Principal Investigator: Walter Matthys, MD, PhD, UMC Utrecht
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
- 05-271
- ZonMw 31100001 (Other Identifier: ZonMw)
- NIDA DA 16135 (Other Identifier: NIDA)
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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