Prevention and Reduction of Alcohol and Drug Problems in a Clinical Psychiatric Youth Population
![]() |
The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details. |
ClinicalTrials.gov Identifier: NCT01595568 |
Recruitment Status : Unknown
Verified July 2012 by Eveline Perrier-Ménard, St. Justine's Hospital.
Recruitment status was: Recruiting
First Posted : May 10, 2012
Last Update Posted : July 19, 2012
|
- Study Details
- Tabular View
- No Results Posted
- Disclaimer
- How to Read a Study Record
In adolescents, mental health problems are frequently associated with substance misuse, even considered a risk factor for alcohol abuse and dependence. This dual diagnosis tends to complicate the patient's treatment and prognosis by increasing, among others, substance use problems, reckless behaviours, relationships and school problems and suicidal thoughts. It is therefore critical to invest time and effort into developing an efficient approach to prevent and reduce substance use problems and offer these children a more global and optimal treatment.
A brief personality-targeted intervention was developed with students of Canadian and English high schools based on four personality factors known to be implicated in the vulnerability to adolescent alcohol misuse (Impulsivity, Anxiety Sensitivity, Negative Thinking and Sensation Seeking) (Conrod et al., 2006,2008, O'Leary-Barrett 2010).
By helping the adolescents to develop better adaptive behaviours, this cognitive-behavioural intervention proved to reduce binge drinking, quantity and frequency of use and substance use problems (Conrod et al., 2006,2011).
The purpose of this study is to assess the impact of this intervention if combined to a regular treatment in a youth psychiatric population.
60 patients aged 14-17 years of a Child and Adolescent psychiatric department will be screened for personality risk with self-report assessments including the Substance Use Risk Profile Scale. Participants will be randomly assigned to a personality matched cognitive-behavioural intervention or a no-intervention control.
The main outcome measures of this study are alcohol and illicit drug outcomes. Secondary measures include mental health symptoms.
Condition or disease | Intervention/treatment | Phase |
---|---|---|
Alcohol Abuse Drug Abuse Mood Disorder Anxiety Disorder Conduct Disorder | Behavioral: Personality-targeted interventions | Not Applicable |
Study Type : | Interventional (Clinical Trial) |
Estimated Enrollment : | 60 participants |
Allocation: | Randomized |
Intervention Model: | Factorial Assignment |
Masking: | None (Open Label) |
Primary Purpose: | Prevention |
Study Start Date : | February 2012 |
Estimated Primary Completion Date : | July 2012 |
Arm | Intervention/treatment |
---|---|
Experimental: Learning to cope with your impulsivity
Cognitive-behavioural intervention targeting impulsive personality
|
Behavioral: Personality-targeted interventions
Motivational and cognitive behavioural interventions targeting four personality profiles. 2 90 minute group sessions with personality-matched peers facilitated by a trained therapist and co-facilitator
Other Names:
|
Experimental: Learning to cope with your sensation seeking
Cognitive behavioural intervention designed to help sensation seeking youth manage their need for stimulation and excitement.
|
Behavioral: Personality-targeted interventions
Motivational and cognitive behavioural interventions targeting four personality profiles. 2 90 minute group sessions with personality-matched peers facilitated by a trained therapist and co-facilitator
Other Names:
|
Experimental: Learning to cope with your anxiety sensitivity
Cognitive behavioural intervention teaching anxiety sensitive youth to manager their sensitivity to threat and anxiety.
|
Behavioral: Personality-targeted interventions
Motivational and cognitive behavioural interventions targeting four personality profiles. 2 90 minute group sessions with personality-matched peers facilitated by a trained therapist and co-facilitator
Other Names:
|
Experimental: Learning to manage your negative thinking
Cognitive behavioural intervention targeting pessimistic and negative thinking in hopeless youth
|
Behavioral: Personality-targeted interventions
Motivational and cognitive behavioural interventions targeting four personality profiles. 2 90 minute group sessions with personality-matched peers facilitated by a trained therapist and co-facilitator
Other Names:
|
- Change in Binge drinking frequency [ Time Frame: Baseline - 4months ]
- Change in Drinking frequency [ Time Frame: Baseline - 4 months ]
- Change in Drinking quantity [ Time Frame: Baseline - 4 months ]
- Change in Drinking problems [ Time Frame: Baseline - 4 months ]
- Change in Emotional and behavioural problems [ Time Frame: Baseline - 4 months ]Psychiatric symptoms (depression, panic anxiety, antisocial behaviours), coping skills, motives for drinking, assessed using the Strengths and Difficulties Questionnaire, the Drinking Motives Questionnaire and the Brief Symptom Inventory.

Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the contacts provided below. For general information, Learn About Clinical Studies.
Ages Eligible for Study: | 14 Years to 17 Years (Child) |
Sexes Eligible for Study: | All |
Accepts Healthy Volunteers: | No |
Inclusion Criteria:
- Motive for psychiatric consultation
- Able to provide consent from parent/guardian for participation in the study

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT01595568
Contact: Eveline Perrier-Ménard, MD | 514-345-4931 ext 4050 | eveline.perrier-menard@umontreal.ca |
Canada, Quebec | |
CHU Ste-Justine | Recruiting |
Montréal, Quebec, Canada, H3T 1C5 | |
Contact eveline.perrier-menard@umontreal.ca |
Responsible Party: | Eveline Perrier-Ménard, MD, Master student, St. Justine's Hospital |
ClinicalTrials.gov Identifier: | NCT01595568 |
Other Study ID Numbers: |
CER CHU Ste-Justine 3435 |
First Posted: | May 10, 2012 Key Record Dates |
Last Update Posted: | July 19, 2012 |
Last Verified: | July 2012 |
Adolescents Dual Diagnosis Mental Disorders Substance Use Problems Prevention |
Disease Alcoholism Substance-Related Disorders Anxiety Disorders Mood Disorders Conduct Disorder |
Pathologic Processes Mental Disorders Alcohol-Related Disorders Chemically-Induced Disorders Attention Deficit and Disruptive Behavior Disorders Neurodevelopmental Disorders |