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Prevention and Reduction of Alcohol and Drug Problems in a Clinical Psychiatric Youth Population

Primary Purpose

Alcohol Abuse, Drug Abuse, Mood Disorder

Status
Unknown status
Phase
Not Applicable
Locations
Canada
Study Type
Interventional
Intervention
Personality-targeted interventions
Personality-targeted interventions
Personality-targeted interventions
Personality-targeted interventions
Sponsored by
St. Justine's Hospital
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Alcohol Abuse focused on measuring Adolescents, Dual Diagnosis, Mental Disorders, Substance Use Problems, Prevention

Eligibility Criteria

14 Years - 17 Years (Child)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Motive for psychiatric consultation
  • Able to provide consent from parent/guardian for participation in the study

Sites / Locations

  • CHU Ste-JustineRecruiting

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm 4

Arm Type

Experimental

Experimental

Experimental

Experimental

Arm Label

Learning to cope with your impulsivity

Learning to cope with your sensation seeking

Learning to cope with your anxiety sensitivity

Learning to manage your negative thinking

Arm Description

Cognitive-behavioural intervention targeting impulsive personality

Cognitive behavioural intervention designed to help sensation seeking youth manage their need for stimulation and excitement.

Cognitive behavioural intervention teaching anxiety sensitive youth to manager their sensitivity to threat and anxiety.

Cognitive behavioural intervention targeting pessimistic and negative thinking in hopeless youth

Outcomes

Primary Outcome Measures

Change in Binge drinking frequency
Change in Drinking frequency
Change in Drinking quantity
Change in Drinking problems

Secondary Outcome Measures

Change in Emotional and behavioural problems
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.

Full Information

First Posted
May 3, 2012
Last Updated
July 18, 2012
Sponsor
St. Justine's Hospital
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1. Study Identification

Unique Protocol Identification Number
NCT01595568
Brief Title
Prevention and Reduction of Alcohol and Drug Problems in a Clinical Psychiatric Youth Population
Study Type
Interventional

2. Study Status

Record Verification Date
July 2012
Overall Recruitment Status
Unknown status
Study Start Date
February 2012 (undefined)
Primary Completion Date
July 2012 (Anticipated)
Study Completion Date
undefined (undefined)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
St. Justine's Hospital

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
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.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Alcohol Abuse, Drug Abuse, Mood Disorder, Anxiety Disorder, Conduct Disorder
Keywords
Adolescents, Dual Diagnosis, Mental Disorders, Substance Use Problems, Prevention

7. Study Design

Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Factorial Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
60 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Learning to cope with your impulsivity
Arm Type
Experimental
Arm Description
Cognitive-behavioural intervention targeting impulsive personality
Arm Title
Learning to cope with your sensation seeking
Arm Type
Experimental
Arm Description
Cognitive behavioural intervention designed to help sensation seeking youth manage their need for stimulation and excitement.
Arm Title
Learning to cope with your anxiety sensitivity
Arm Type
Experimental
Arm Description
Cognitive behavioural intervention teaching anxiety sensitive youth to manager their sensitivity to threat and anxiety.
Arm Title
Learning to manage your negative thinking
Arm Type
Experimental
Arm Description
Cognitive behavioural intervention targeting pessimistic and negative thinking in hopeless youth
Intervention Type
Behavioral
Intervention Name(s)
Personality-targeted interventions
Other Intervention Name(s)
Preventure, Adventure
Intervention Description
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
Intervention Type
Behavioral
Intervention Name(s)
Personality-targeted interventions
Other Intervention Name(s)
Preventure, Adventure
Intervention Description
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
Intervention Type
Behavioral
Intervention Name(s)
Personality-targeted interventions
Other Intervention Name(s)
Preventure, Adventure
Intervention Description
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
Intervention Type
Behavioral
Intervention Name(s)
Personality-targeted interventions
Other Intervention Name(s)
Preventure, Adventure
Intervention Description
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
Primary Outcome Measure Information:
Title
Change in Binge drinking frequency
Time Frame
Baseline - 4months
Title
Change in Drinking frequency
Time Frame
Baseline - 4 months
Title
Change in Drinking quantity
Time Frame
Baseline - 4 months
Title
Change in Drinking problems
Time Frame
Baseline - 4 months
Secondary Outcome Measure Information:
Title
Change in Emotional and behavioural problems
Description
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.
Time Frame
Baseline - 4 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
14 Years
Maximum Age & Unit of Time
17 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Motive for psychiatric consultation Able to provide consent from parent/guardian for participation in the study
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Eveline Perrier-Ménard, MD
Phone
514-345-4931
Ext
4050
Email
eveline.perrier-menard@umontreal.ca
Facility Information:
Facility Name
CHU Ste-Justine
City
Montréal
State/Province
Quebec
ZIP/Postal Code
H3T 1C5
Country
Canada
Individual Site Status
Recruiting
Facility Contact:
Email
eveline.perrier-menard@umontreal.ca

12. IPD Sharing Statement

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Prevention and Reduction of Alcohol and Drug Problems in a Clinical Psychiatric Youth Population

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