Clinical Trials Directory

Trials / Completed

CompletedNCT01253993

Impaired Decision-making in Adolescents

Impaired Decision-making in Adolescents: A Vulnerability Factor for the Development of Substance Use and Abuse.

Status
Completed
Phase
Study type
Observational
Enrollment
152 (actual)
Sponsor
UMC Utrecht · Academic / Other
Sex
All
Age
14 Years – 21 Years
Healthy volunteers
Accepted

Summary

There is clear evidence that aggressive behavior and disruptive behavior disorders (DBD) in middle childhood are associated with an increased risk for substance abuse in adolescence. However, the exact underlying mechanism of this increased risk is unknown. It is likely that a biopsychological vulnerability in some aggressive children and children with DBD makes them liable to substance use and abuse. The investigators hypothesize that deficient decision making is such a biopsychological factor. In this study the investigators aim to test the latter hypothesis by investigating the decision making ability in a group of adolescents with DBD with and without substance use disorders. Decision-making is assessed with the IOWA Gambling Task (GT). This task mimics real-life situations in the way it factors uncertainty, reward and punishment. The GT is specifically designed to assess impaired decision-making in individuals who are unable to learn from their mistakes and make decisions that repeatedly lead to negative consequences. This characteristic may be common to individuals with externalizing disorders such as DBD, psychopathy, and substance use disorders.

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.

Conditions

Timeline

Start date
2006-04-01
Primary completion
2007-06-01
Completion
2007-09-01
First posted
2010-12-06
Last updated
2010-12-06

Locations

1 site across 1 country: Netherlands

Source: ClinicalTrials.gov record NCT01253993. Inclusion in this directory is not an endorsement.