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The UniVenture Program

Primary Purpose

Anxiety Sensitivity, Hopelessness, Sensation Seeking

Status
Recruiting
Phase
Not Applicable
Locations
Canada
Study Type
Interventional
Intervention
UniVenture Hopelessness manual
UniVenture Anxiety Sensitivity manual
UniVenture Sensation Seeking manual
UniVenture Impulsivity manual
Service as usual provided by the University
Sponsored by
Sherry Stewart
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Anxiety Sensitivity focused on measuring Substance misuse, Prevention, Personality, Knowledge mobilization, Well-being, Academic retention, Academic performance, Binge drinking, Emerging adulthood, Life transitions, Technology assisted programs, Student services

Eligibility Criteria

18 Years - 25 Years (Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

  • 1st and 2nd year undergraduate students (either part-time or full-time enrollment)
  • Age between 18- 25 years
  • Have used alcohol and/or cannabis and/or any other substance in the past 3 months,
  • Score at least 0.5 standard deviation (SD) above the population-specific norm on 1 of 4 personality traits on the Substance Use Risk Profile Scale (SURPS) (i) Anxiety Sensitivity (AS) (ii) Hopelessness (HOP) (iii) Sensation Seeking (SS) and (iv) Impulsive (IMP)

Exclusion Criteria:

• Unwilling to participate

Sites / Locations

  • University of British Columbia-Okanagan campusRecruiting
  • St. Francis Xavier UniversityRecruiting
  • Dalhousie UniversityRecruiting
  • York UniversityRecruiting
  • Université de MontréalRecruiting

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm Type

Experimental

Active Comparator

Placebo Comparator

Arm Label

UniVenture- face-to-face (in-person format)

UniVenture- online (distance-delivery format)

UniVenture- service as usual (control)

Arm Description

Personality-matched wellness program condition in face-to-face format (i.e., high AS student receives face-to-face AS program; high HOP student receives face-to-face HOP workshop: high SS student receives face-to-face SS workshop; high IMP student receives face-to-face IMP workshop)

Personality-matched wellness program condition in distance-delivery format (i.e., high AS student receives online (distance-delivered) AS workshop; high HOP student receives online (distance-delivered) HOP workshop: high SS student receives online (distance-delivered) SS workshop; high IMP student receives online (distance-delivered) IMP workshop

Services-as-usual offered by the respective university

Outcomes

Primary Outcome Measures

Changes in alcohol-related harms in undergraduates
Alcohol use as a continuous measure of alcohol-related harm. The Brief-Young Adult Alcohol Consequences Questionnaire (B-YAACQ) is a 24-item scale that will be used to measure changes in the experiences of alcohol-related harms in the past 3 months. The response options include (1) Yes, in the past 3 months, (2) Yes, but not in the past 3 months (3) No. This measure will be scored as the number of adverse consequences experienced in the last three months on a continuous scale from 0-24. [Higher scores indicate greater adverse alcohol consequences]
Changes in cannabis-related harms in undergraduates
Cannabis use as a continuous measure of cannabis-related harm. The Brief Marijuana Consequences Questionnaire (BMACQ) is a 21-item scale that will be used to measure changes in participants' reported experiences of cannabis-related harms in the past 3 months. The response options include (1) Yes, in the past 3 months, (2) Yes, but not in the past 3 months (3) No. This measure will be scored as the number of adverse consequences experienced in the last three months on a continuous scale from 0-21. [Higher scores indicate greater adverse cannabis consequences]
Changes in the student wellbeing in undergraduates
It will be measured by the Patient Health Questionnaire Anxiety-Depression Scale (PHQ-ADS) - which combines the Patient Health Questionnaire (PHQ-9) and Generalized Anxiety Disorder (GAD-7) scales - as a composite measure of depression and anxiety. Response option of Generalized Anxiety Disorder (GAD-7) is (1) Not at all (2) Several days (3) More than half of the days (4) Nearly every day. Response option of Patient Health Questionnaire (PHQ-9) is (1) Not at all (2) Several days (3) Over half the days (4) Nearly every day. [Higher scores indicate higher mental wellbeing]

Secondary Outcome Measures

Differences in semester GPA between treatment groups.
Semester-wise grade point average [GPA] as a proxy of Undergraduates' academic performance (i.e., objective indices of grades). GPA data retrieved from the registrar's office at each site will be converted to a common 6-point GPA scale since different university sites use different GPA scales (%, 5-point GPA, 9-point GPA). The scale ranges from 1 to 6 where 1 indicates lower performance and 6 indicates higher performance. [Higher scores indicate higher GPA in that semester.]
Changes in scores on the undergraduates' Academic retention measure
Measured by the 6-item self-reported Academic outcome survey: Academic experience scale. Item response options include (1) Strongly disagree (2) Disagree (3) Neither agree nor disagree (4) Agree (5) Strongly agree. A total score is derived by summing scores across the 6 items. [Higher scores indicate higher academic retention].
Changes in scores on the undergraduates' Academic challenges measure
This is assessed with a 35-item Academic outcome survey. This composite score [Self-Regulated Learning -Challenges Scale (SRL-C)] will represent the academic challenges experienced. Item response options range from: (1) Strongly disagree to (5) Strongly agree. The composite score is comprised of five areas of academic challenges typically reported by undergraduate students: (1) Motivation (e.g., challenges initiating and sustaining engagement); (2) Goal and time management (e.g., challenges making deadlines, or managing priorities) (3) Cognitive (challenges maintaining focus, understanding course material (4) Socio-emotional (challenges adjusting to new academic expectations; balancing health and well-being); and (5) Meta-cognitive (challenges setting goals or choosing strategies). [Higher scores on the composite indicate greater levels of academic challenges being experienced by the student.]
Changes in scores on the undergraduate self-regulated learning (SRL) behaviour measure and Self-efficacy beliefs for undergraduates' success measures
Two separate scales [SRL Self-Regulated Learning -Practices Scale (SRL-P) and Self-Regulated Learning -Challenges Scale (SRL-C)] will be combined and consist of 35 items from the Academic outcome survey with response options of (1) Strongly disagree (2) Disagree (3) Neutral (4) Agree (5) Strongly agree. [Higher scores indicate more proactive self-regulated learning behaviours/practices and indicate stronger belief about academic success]
Changes in score of hazardous drinkers in undergraduates
This 3-item The Alcohol Use Disorders Identification Test Consumption screening tool (AUDIT-C) questions (composite score) capture individuals who are hazardous drinkers or who have alcohol use disorders (including alcohol abuse or dependence). It is scored on a scale of 0-12 points (each item has maximum of 4 score where 0 reflect no alcohol use). In men, a score of 4 points or more is considered positive for alcohol misuse; in women, a score of 3 points or more is considered positive. Generally, the higher the AUDIT-C score, the higher the likelihood of affecting health and safety due to individual's drinking.

Full Information

First Posted
September 27, 2021
Last Updated
May 24, 2022
Sponsor
Sherry Stewart
Collaborators
Dalhousie University, St. Francis Xavier University, Université de Montréal, York University, University of British Columbia, University of Victoria, Canadian Centre on Substance Use and Addiction (CCSA), Canadian Research Initiative in Substance Misuse, Injury Free Nova Scotia (IFNS), Mental Health Commission of Canada (MHCC), Postsecondary Education Partnership - Alcohol Harms (PEP-AH), Strategy for Patient Orientated Research, SHARP- Students for Healthy Alternatives & Risk Prevention, Nova Scotia Health Authority
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1. Study Identification

Unique Protocol Identification Number
NCT05383989
Brief Title
The UniVenture Program
Official Title
UniVenture: A Partnership to Address Heavy Drinking and Other Substance Misuse on Canadian University Campuses
Study Type
Interventional

2. Study Status

Record Verification Date
May 2022
Overall Recruitment Status
Recruiting
Study Start Date
September 11, 2021 (Actual)
Primary Completion Date
February 8, 2024 (Anticipated)
Study Completion Date
July 1, 2024 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor-Investigator
Name of the Sponsor
Sherry Stewart
Collaborators
Dalhousie University, St. Francis Xavier University, Université de Montréal, York University, University of British Columbia, University of Victoria, Canadian Centre on Substance Use and Addiction (CCSA), Canadian Research Initiative in Substance Misuse, Injury Free Nova Scotia (IFNS), Mental Health Commission of Canada (MHCC), Postsecondary Education Partnership - Alcohol Harms (PEP-AH), Strategy for Patient Orientated Research, SHARP- Students for Healthy Alternatives & Risk Prevention, Nova Scotia Health Authority

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
UniVenture is a research partnership with one common goal: to adapt, test, and begin sharing an effective, sustainable, targeted wellness program to tackle the timely social issue of heavy drinking and other substance misuse on Canadian campuses. Our project is a 5-year, multi-site, controlled study involving 1st and 2nd year undergraduates at 5 representatively diverse Canadian university sites (Dalhousie University, St. Francis Xavier University, York University, Université de Montréal, and University of British Columbia-Okanagan). The investigator will test a program targeting personality traits linked to substance misuse. An earlier version of this program led to marked reductions in substance use and distress in adolescents. Our novel objectives are to examine the program's effects on substance use and distress among emerging adults; uptake of prescription drug use given the opioid crisis; and undergraduates' academic success. The investigator will carry out a randomized controlled trail in which two versions of the program will be assessed: a face-to-face and an innovative and accessible technology-assisted distance-delivery format, both compared to normal campus services alone. UniVenture may potentially have a dramatic effect on university policies on the prevention of substance misuse on Canadian campuses by helping partners appreciate the effectiveness of targeted and personalized approaches, and leveraging partners' expansive networks to inform other Canadian universities. A successful technology-assisted distance-delivered program will provide universities with an effective, relatively low-cost, and accessible tool to intervene with risky substance use behaviors in undergraduates. A successful program for at-risk students will also profoundly impact their academic performance and goal achievement, as well as their lives beyond university. Our partnership will impact knowledge sharing and student training opportunities. With a diversity of academic and non-academic partners and an integrative knowledge sharing approach, the investigator will share results with many audiences throughout the project. The academic researchers have recognized expertise in training and mentoring students. Further, trainees will be exposed to many opportunities and settings both inside and outside of the university in which to apply their research skills to substance misuse prevention.
Detailed Description
The UniVenture program is a wellness program designed for university students, to be tested at 5 university-based sites (Dalhousie University, St. Francis Xavier University, York University, Université de Montréal, and University of British Columbia-Okanagan), and based on an existing, successful, and internationally recognized and -utilized program called PreVenture (designed for high school students). PreVenture is a selective personality-targeted approach based on an etiologic model of substance misuse behaviors, outlined and validated by Drs. Stewart (Project Director [PD]) and Conrod (Co-Applicant [CA]). PreVenture targets personality-specific motivational pathways to substance misuse, AS, HOP, SS, and IMP, each associated with different motives for substance use, substance use profiles, and patterns of emotional distress and risk-taking. Well-controlled studies show PreVenture reduces or delays teens' binge drinking, illicit drug use, and associated emotional problems by 30-80% with effects lasting at least 2 years. While PreVenture: (a) was designed for and is effective for high school students, its efficacy in university students is untested; (b) is effective for alcohol and cannabis use, its effects on prescription drug misuse are unknown; and (c) works to reduce student distress, it is untested for preventing academic struggles and university drop out. These latter academic outcomes are of major concern to our Student Affairs partners given the current shockingly high university drop-out rates (18.7-36.9%) and strong ties of student substance misuse and distress with poorer academic outcomes. The purpose of the UniVenture study is to measure the efficacy the developmentally adapted program has on primary outcomes of (1) Reduction of alcohol-related harms in undergraduates (2) Reduction of cannabis-related harms in undergraduates (3) Changes in the student wellbeing in undergraduates. Secondary outcomes are (1) Differences in semester GPA between treatment groups. (2) Changes in scores on the undergraduates' Academic retention measure (3) Changes in scores on the undergraduates' Academic challenges measure (4) Changes in scores on the undergraduate self-regulated learning (SRL) behaviour measure and Self-efficacy beliefs for undergraduates' success measures (5) Reduction in score of hazardous drinkers in undergraduates. Barriers to accessing evidence-based programs contribute to the ineffectiveness of campus-based substance misuse prevention. These barriers include students' time commitments, lack of available services, fear of stigma, and long wait lists which may discourage students from seeking or engaging in existing programs, leading to more severe problems before participants receive help. A distance-delivery approach involves using remote communication technologies (e.g., web-based, email, chat) to link students with a facilitator in place of face-to-face meetings. This may improve access for those with difficulties getting to services or increase confidentiality through engagement from a private location. The investigator proposes a novel randomized controlled study to test the relative effects of our personality-targeted wellness program on hazardous drinking, cannabis use, and uptake of prescription drug misuse among high-personality-risk 1st and 2nd year undergraduates and delivered in 2 formats: traditional face-to-face vs. an innovative and more accessible technology-assisted distance-delivery by well-trained and supervised program facilitators. These two active program conditions will be compared to a services-as-usual only control condition to evaluate how this program compares to what Student Affairs unit partners already do. Withholding the program from at-risk undergraduates randomized to the services-as-usual only control group might be seen as problematic; however, the program's efficacy is untested at the emerging adulthood (EA) developmental stage and in the university context. If the distance-delivered program is shown effective, control condition participants will be sent a free link to the relevant personality-matched web-based materials after the 12-month follow-up.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Anxiety Sensitivity, Hopelessness, Sensation Seeking, Impulsivity
Keywords
Substance misuse, Prevention, Personality, Knowledge mobilization, Well-being, Academic retention, Academic performance, Binge drinking, Emerging adulthood, Life transitions, Technology assisted programs, Student services

7. Study Design

Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
A personality-matched wellness program condition in face-to-face format (i.e., high AS student receives face-to-face AS program; high HOP student receives face-to-face HOP workshop: high SS student receives face-to-face SS workshop; high IMP student receives face-to-face IMP workshop) A personality-matched wellness program condition in distance-delivery format (i.e., high AS student receives distance-delivered AS workshop; etc. as per the face-to-face format). Services-as-usual offered by the respective university
Masking
Outcomes Assessor
Allocation
Randomized
Enrollment
1000 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
UniVenture- face-to-face (in-person format)
Arm Type
Experimental
Arm Description
Personality-matched wellness program condition in face-to-face format (i.e., high AS student receives face-to-face AS program; high HOP student receives face-to-face HOP workshop: high SS student receives face-to-face SS workshop; high IMP student receives face-to-face IMP workshop)
Arm Title
UniVenture- online (distance-delivery format)
Arm Type
Active Comparator
Arm Description
Personality-matched wellness program condition in distance-delivery format (i.e., high AS student receives online (distance-delivered) AS workshop; high HOP student receives online (distance-delivered) HOP workshop: high SS student receives online (distance-delivered) SS workshop; high IMP student receives online (distance-delivered) IMP workshop
Arm Title
UniVenture- service as usual (control)
Arm Type
Placebo Comparator
Arm Description
Services-as-usual offered by the respective university
Intervention Type
Behavioral
Intervention Name(s)
UniVenture Hopelessness manual
Intervention Description
Intended for those who score at least 0.5 standard deviation (SD) above the population-specific norm on Hopelessness (HOP) personality traits on the Substance Use Risk Profile Scale (SURPS).
Intervention Type
Behavioral
Intervention Name(s)
UniVenture Anxiety Sensitivity manual
Intervention Description
Intended for those who score at least 0.5 standard deviation (SD) above the population-specific norm on Anxiety Sensitivity (AS) personality traits on the Substance Use Risk Profile Scale (SURPS).
Intervention Type
Behavioral
Intervention Name(s)
UniVenture Sensation Seeking manual
Intervention Description
Intended for those who score at least 0.5 standard deviation (SD) above the population-specific norm on Sensation Seeking (SS) personality traits on the Substance Use Risk Profile Scale (SURPS)
Intervention Type
Behavioral
Intervention Name(s)
UniVenture Impulsivity manual
Intervention Description
Intended for those who score at least 0.5 standard deviation (SD) above the population-specific norm on Impulsivity (IMP) personality traits on the Substance Use Risk Profile Scale (SURPS).
Intervention Type
Behavioral
Intervention Name(s)
Service as usual provided by the University
Intervention Description
It is the regular university-provided well-being services.
Primary Outcome Measure Information:
Title
Changes in alcohol-related harms in undergraduates
Description
Alcohol use as a continuous measure of alcohol-related harm. The Brief-Young Adult Alcohol Consequences Questionnaire (B-YAACQ) is a 24-item scale that will be used to measure changes in the experiences of alcohol-related harms in the past 3 months. The response options include (1) Yes, in the past 3 months, (2) Yes, but not in the past 3 months (3) No. This measure will be scored as the number of adverse consequences experienced in the last three months on a continuous scale from 0-24. [Higher scores indicate greater adverse alcohol consequences]
Time Frame
Past 3 months
Title
Changes in cannabis-related harms in undergraduates
Description
Cannabis use as a continuous measure of cannabis-related harm. The Brief Marijuana Consequences Questionnaire (BMACQ) is a 21-item scale that will be used to measure changes in participants' reported experiences of cannabis-related harms in the past 3 months. The response options include (1) Yes, in the past 3 months, (2) Yes, but not in the past 3 months (3) No. This measure will be scored as the number of adverse consequences experienced in the last three months on a continuous scale from 0-21. [Higher scores indicate greater adverse cannabis consequences]
Time Frame
Past 3 months
Title
Changes in the student wellbeing in undergraduates
Description
It will be measured by the Patient Health Questionnaire Anxiety-Depression Scale (PHQ-ADS) - which combines the Patient Health Questionnaire (PHQ-9) and Generalized Anxiety Disorder (GAD-7) scales - as a composite measure of depression and anxiety. Response option of Generalized Anxiety Disorder (GAD-7) is (1) Not at all (2) Several days (3) More than half of the days (4) Nearly every day. Response option of Patient Health Questionnaire (PHQ-9) is (1) Not at all (2) Several days (3) Over half the days (4) Nearly every day. [Higher scores indicate higher mental wellbeing]
Time Frame
Past 3 months
Secondary Outcome Measure Information:
Title
Differences in semester GPA between treatment groups.
Description
Semester-wise grade point average [GPA] as a proxy of Undergraduates' academic performance (i.e., objective indices of grades). GPA data retrieved from the registrar's office at each site will be converted to a common 6-point GPA scale since different university sites use different GPA scales (%, 5-point GPA, 9-point GPA). The scale ranges from 1 to 6 where 1 indicates lower performance and 6 indicates higher performance. [Higher scores indicate higher GPA in that semester.]
Time Frame
Through study completion, an average of 1 year
Title
Changes in scores on the undergraduates' Academic retention measure
Description
Measured by the 6-item self-reported Academic outcome survey: Academic experience scale. Item response options include (1) Strongly disagree (2) Disagree (3) Neither agree nor disagree (4) Agree (5) Strongly agree. A total score is derived by summing scores across the 6 items. [Higher scores indicate higher academic retention].
Time Frame
Through study completion, an average of 1 year
Title
Changes in scores on the undergraduates' Academic challenges measure
Description
This is assessed with a 35-item Academic outcome survey. This composite score [Self-Regulated Learning -Challenges Scale (SRL-C)] will represent the academic challenges experienced. Item response options range from: (1) Strongly disagree to (5) Strongly agree. The composite score is comprised of five areas of academic challenges typically reported by undergraduate students: (1) Motivation (e.g., challenges initiating and sustaining engagement); (2) Goal and time management (e.g., challenges making deadlines, or managing priorities) (3) Cognitive (challenges maintaining focus, understanding course material (4) Socio-emotional (challenges adjusting to new academic expectations; balancing health and well-being); and (5) Meta-cognitive (challenges setting goals or choosing strategies). [Higher scores on the composite indicate greater levels of academic challenges being experienced by the student.]
Time Frame
Past 2 weeks
Title
Changes in scores on the undergraduate self-regulated learning (SRL) behaviour measure and Self-efficacy beliefs for undergraduates' success measures
Description
Two separate scales [SRL Self-Regulated Learning -Practices Scale (SRL-P) and Self-Regulated Learning -Challenges Scale (SRL-C)] will be combined and consist of 35 items from the Academic outcome survey with response options of (1) Strongly disagree (2) Disagree (3) Neutral (4) Agree (5) Strongly agree. [Higher scores indicate more proactive self-regulated learning behaviours/practices and indicate stronger belief about academic success]
Time Frame
Past 2 weeks
Title
Changes in score of hazardous drinkers in undergraduates
Description
This 3-item The Alcohol Use Disorders Identification Test Consumption screening tool (AUDIT-C) questions (composite score) capture individuals who are hazardous drinkers or who have alcohol use disorders (including alcohol abuse or dependence). It is scored on a scale of 0-12 points (each item has maximum of 4 score where 0 reflect no alcohol use). In men, a score of 4 points or more is considered positive for alcohol misuse; in women, a score of 3 points or more is considered positive. Generally, the higher the AUDIT-C score, the higher the likelihood of affecting health and safety due to individual's drinking.
Time Frame
Past 3 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
25 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: 1st and 2nd year undergraduate students (either part-time or full-time enrollment) Age between 18- 25 years Have used alcohol and/or cannabis and/or any other substance in the past 3 months, Score at least 0.5 standard deviation (SD) above the population-specific norm on 1 of 4 personality traits on the Substance Use Risk Profile Scale (SURPS) (i) Anxiety Sensitivity (AS) (ii) Hopelessness (HOP) (iii) Sensation Seeking (SS) and (iv) Impulsive (IMP) Exclusion Criteria: • Unwilling to participate
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Fakir Md Yunus
Phone
306-514-0055
Email
fakir.yunus@dal.ca
First Name & Middle Initial & Last Name or Official Title & Degree
Jennifer E Swansburg
Phone
902-494-3793
Email
jennifer.swansburg@dal.ca
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Sherry H Stewart
Organizational Affiliation
Dalhousie University
Official's Role
Study Director
First Name & Middle Initial & Last Name & Degree
Patricia Conrod
Organizational Affiliation
Université de Montréal
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Kara Thompson
Organizational Affiliation
St. Francis Xavier University
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Matthew T Keough
Organizational Affiliation
York University
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Marvin Krank
Organizational Affiliation
University of British Columbia- Okanagan
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Allyson Hadwin
Organizational Affiliation
University of Victoria
Official's Role
Principal Investigator
Facility Information:
Facility Name
University of British Columbia-Okanagan campus
City
Kelowna
State/Province
British Columbia
Country
Canada
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Cassidy RD Wallis, MA
Email
cassidywallis13@gmail.com
First Name & Middle Initial & Last Name & Degree
Katherine Rose, MA
Email
katherine.rose@ubc.ca
Facility Name
St. Francis Xavier University
City
Antigonish
State/Province
Nova Scotia
Country
Canada
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Stephanie Cooper
Email
scooper@stfx.ca
Facility Name
Dalhousie University
City
Halifax
State/Province
Nova Scotia
Country
Canada
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Fakir Md Yunus, PhD
Phone
306-514-0055
Email
fakir.yunus@dal.ca
First Name & Middle Initial & Last Name & Degree
Jennifer E Swansburg
Phone
902-494-3793
Email
jennifer.swansburg@dal.ca
Facility Name
York University
City
Toronto
State/Province
Ontario
Country
Canada
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Matthew Keough, PhD
Email
keoughmt@yorku.ca
Facility Name
Université de Montréal
City
Montréal
State/Province
Quebec
Country
Canada
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Patricia Conrod, PhD
Email
Patricia.conrod@umontreal.ca
First Name & Middle Initial & Last Name & Degree
Natalie Castellanos-Ryan, PhD

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
Citation
Szalavitz, M. (2016, September 29). The 4 traits that put kids at risk for addiction. The New York Times. Retrieved from https://www.nytimes.com/2016/10/04/well/family/the-4-traits-that-put-kids-at- risk-for-addiction.html
Results Reference
background
Citation
Nair, R. (2017, January 22). Vernon, B. C. schools to pilot program that identifies addiction personality traits. CBC News. Retrieved from https://www.cbc.ca/news/canada/british-columbia/vernon-b- c-schools-to-pilot-program-thatidentifies-addiction-personality-traits-1.3942792
Results Reference
background
Citation
UNESCO, UNODC, & WHO. (2017). Education sector responses to the use of alcohol, tobacco and drugs. In the UNESCO series Good Policy and Practice in Health Education. Retrieved from http://www.who.int/substance_abuse/activities/education_sector/en/
Results Reference
background
PubMed Identifier
28252892
Citation
Substance Abuse and Mental Health Services Administration (US); Office of the Surgeon General (US). Facing Addiction in America: The Surgeon General's Report on Alcohol, Drugs, and Health [Internet]. Washington (DC): US Department of Health and Human Services; 2016 Nov. Available from http://www.ncbi.nlm.nih.gov/books/NBK424857/
Results Reference
background
PubMed Identifier
17007600
Citation
Conrod PJ, Stewart SH, Comeau N, Maclean AM. Efficacy of cognitive-behavioral interventions targeting personality risk factors for youth alcohol misuse. J Clin Child Adolesc Psychol. 2006 Dec;35(4):550-63. doi: 10.1207/s15374424jccp3504_6.
Results Reference
background
PubMed Identifier
19683400
Citation
Woicik PA, Stewart SH, Pihl RO, Conrod PJ. The Substance Use Risk Profile Scale: a scale measuring traits linked to reinforcement-specific substance use profiles. Addict Behav. 2009 Dec;34(12):1042-55. doi: 10.1016/j.addbeh.2009.07.001. Epub 2009 Jul 8.
Results Reference
background
Citation
Castellanos-Ryan, N., & Conrod, P. J. (2012). Personality and substance misuse: Evidence for a four-factor model of vulnerability. In Verster, J. C., Brady, K., Galanter, M., & Conrod, P. J. (Eds.), Drug abuse and addiction in medical illness: Causes, consequences and treatment (pp. 47-62). New York: Springer.
Results Reference
background
Citation
Stewart, S. H., Grant, V. V., Mackie, C. J., & Conrod, P. J. (2016). Comorbidity of anxiety and depression with substance use disorders. In K. Sher (Ed.), The Oxford Handbook of Substance Use Disorders. New York: Oxford University Press.
Results Reference
background
PubMed Identifier
10998950
Citation
Conrod PJ, Pihl RO, Stewart SH, Dongier M. Validation of a system of classifying female substance abusers on the basis of personality and motivational risk factors for substance abuse. Psychol Addict Behav. 2000 Sep;14(3):243-56. doi: 10.1037//0893-164x.14.3.243.
Results Reference
background
PubMed Identifier
18211277
Citation
Conrod PJ, Castellanos N, Mackie C. Personality-targeted interventions delay the growth of adolescent drinking and binge drinking. J Child Psychol Psychiatry. 2008 Feb;49(2):181-90. doi: 10.1111/j.1469-7610.2007.01826.x.
Results Reference
background
PubMed Identifier
20048226
Citation
Conrod PJ, Castellanos-Ryan N, Strang J. Brief, personality-targeted coping skills interventions and survival as a non-drug user over a 2-year period during adolescence. Arch Gen Psychiatry. 2010 Jan;67(1):85-93. doi: 10.1001/archgenpsychiatry.2009.173.
Results Reference
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PubMed Identifier
20732631
Citation
O'Leary-Barrett M, Mackie CJ, Castellanos-Ryan N, Al-Khudhairy N, Conrod PJ. Personality-targeted interventions delay uptake of drinking and decrease risk of alcohol-related problems when delivered by teachers. J Am Acad Child Adolesc Psychiatry. 2010 Sep;49(9):954-963.e1. doi: 10.1016/j.jaac.2010.04.011. Epub 2010 Jul 31.
Results Reference
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