Comparing the Effect of Adding a Remote Self-reporting Tool for Distress and Fit-for-purpose Mental Health & Addictions Service to Usual Case Management on Dropout Rates in a Vocational Training Program

Overview

Youth unemployment is a chronic problem in most societies. Some young adults are neither in employment, eduction or training (NEET), and are at high risk of chronic unemployment, social disengagement and poor quality of life. Identifying this high risk population and providing them with career skills training and opportunities is critical for their full participation in society. Vocational training programs provide an opportunity for these NEET youth to develop a skilled trade. Barriers to successful completion of these programs include high prevalence of mental health and substance use disorders among NEET youth. This study will use a daily self-report distress tool to identify vocational program trainees at risk of absence or drop-out due to mental health and/or substance abuse issues. These at-risk trainees will then be referred to a mental health crisis program through a fit-for-purpose referral process to accommodate their training program requirements. It is hypothesized that early identification and referral for mental health and substance abuse issues will reduce both program absence and drop-out rates and result in improved in long-term employment for these NEET youth.

Full Title of Study: “A Cluster Randomized, 2×2 Factorial, Superiority Study to Compare the Effectiveness of Adding a Remote Self-reporting Tool for Distress and a Fit-for-purpose Mental Health & Addictions Service to Usual Case Management on Program Completion and Employment Among Unemployed Visible Minorities and Women Enrolled in a Vocational Training Program”

Study Type

  • Study Type: Interventional
  • Study Design
    • Allocation: Randomized
    • Intervention Model: Factorial Assignment
    • Primary Purpose: Health Services Research
    • Masking: None (Open Label)
  • Study Primary Completion Date: January 15, 2026

Detailed Description

The Trades & Diversity Training Program (TDTP) is a Canadian federal government-funded vocational construction skills training program for visible minority & female youth who are chronically under- and unemployed. The TDTP is a 12-week program that includes both in-classroom education and supervised hands-on experiential learning at participating construction sites. The trainees are supported by a case manager who identifies, plans and co-ordinates support services to minimize program absences and drop-out. The most significant barriers to successful program completion and long-term employment are mental health and substance use disorders. Historically, identification and rapid referral to mental health and addiction services has been difficult due to human resource limitations and limited access to timely healthcare services. This study will randomize cohorts enrolled in each 12-week training program located in 2 sites to the use of a self-report distress tool versus usual case management. The distress tool is a web-based self-reporting tool that is accessed by trainees on a daily basis to report their distress levels, the underlying reasons for this distress and whether this distress will prevent them from attending class or put them at-risk for drop-out. For those individuals whose distress levels threaten their program participation, the case manager is alerted immediately via an email notification. The case manager is then responsible for connecting with the trainees and engaging the rapid referral process for mental health and addictions healthcare services. The control cohorts will receive the usual case management approach of engaging students on an intermittent basis and providing support as needed.

Interventions

  • Behavioral: Basic Case Management
    • Usual case management support during 12-week training program
  • Behavioral: Basic Case Management plus Distress Tool
    • Usual case management support during 12-week training program plus daily self-reports of distress using Distress Thermometer tool
  • Behavioral: Basic Case Management plus rapid mental health & addictions healthcare access
    • Usual case management support during 12-week training program plus rapid access referral process for healthcare crisis services
  • Behavioral: Basic Case Management plus Distress Tool and rapid mental health & addictions healthcare access
    • Usual case management support during 12-week training program plus daily distress self-reports plus rapid access referral process for healthcare crisis services

Arms, Groups and Cohorts

  • Active Comparator: Basic case management
    • Basic case management with bi-weekly meetings between case manager and trainees that includes check-ins, frequent visits to construction sites and monitoring of feedback forms from mentors. Case managers attempt to connect trainees with external support services as needed.
  • Experimental: Basic case management supplemented by self-reporting distress tool (DT)
    • Basic case management plus access to the self-report daily distress tool. The trainees are provided web-based access to the daily distress tool and report their distress levels using a validated visual analog scale (Distress Thermometer), along with reporting their risk of missing work/class or dropping out of the program. The case manager responds to the distress tool by coordinating external support services as needed.
  • Experimental: Basic case management supplemented by rapid access healthcare services
    • Basic case management supplemented by a fit-for-purpose rapid referral process for trainees with active mental health and/or substance use disorders affecting their program participation.
  • Experimental: Basic case management supplemented by DT and rapid access healthcare services
    • Basic case management supplemented by both the self-report distress tool and rapid referral process for those trainees at-risk of program absence or drop-out from either mental health or addictions issues.

Clinical Trial Outcome Measures

Primary Measures

  • Program attendance
    • Time Frame: 12 weeks from program enrolment
    • Difference in proportion of absence-free program days, where absence-free day is defined as being present in class or work setting by case manager or supervisor. Maximum number of absence-free days is 48 days (12 weeks x 4-day work week). A day is defined as an 8- to 10-hour work day from Monday to Thursday.
  • Program completion
    • Time Frame: 12 weeks from program enrolment
    • Difference in proportion of drop-outs, where a drop-out is defined as an apprentice who fulfils any of the following criteria: Has missed more than 50% of class/work days, or Who has elected to leave the program for reasons other than taking another job or returning to school
  • Post-program employment
    • Time Frame: 24 weeks post-program completion
    • Difference in proportion of full-time employment, where full-time employment is defined as paid work ≥ 30 (median) hours per week at their main or only job. The reference period that will be used to determine full-time employment is the 4-week period preceding the 24-month post-program completion date.

Secondary Measures

  • Access to healthcare services
    • Time Frame: 12 weeks from program enrolment
    • Difference in time to access mental health & addiction services, where time to access is defined as the difference (hours) between the date of referral from the case manager to the date of the mental health & addictions appointment/assessment.
  • Healthcare utilization
    • Time Frame: 12 weeks from program enrolment
    • Difference in incidence rates of healthcare days, where healthcare days represent the number of days alive and registered for an emergency room, mental health outpatient or addictions outpatient visit, or admitted to an acute care, mental health or detoxification facility. The potential number of healthcare days is the number of days alive during the program (12 weeks x 7 days = 84 days)
  • Apprentice satisfaction
    • Time Frame: 12 weeks from program enrolment
    • Difference in program satisfaction scores, where program satisfaction scores will be measured using the validated National Centre for Vocational Education Research Student Outcomes Survey Satisfaction scores
  • Acceptability of self-report distress tool
    • Time Frame: 12 weeks from program enrolment
    • To measure the acceptability of using the Distress Thermometer screening tool by apprentices and the case manager, where acceptability is measured using a validated 2-item questionnaire.
  • Feasibility of self-report distress tool
    • Time Frame: 12 weeks from program enrolment
    • To measure the feasibility of using the Distress Thermometer screening tool by apprentices and the case manager, where feasibility is measured using a validated 1-item questionnaire.
  • Compliance of self-report distress tool
    • Time Frame: 12 weeks from program enrolment
    • To measure apprentices’ compliance with the Distress Thermometer screening tool, where compliance is defined as the ratio of completed daily screens relative to the total number of program days

Participating in This Clinical Trial

Inclusion Criteria

  • must be a visible minority or female – must be fluent in English or French – must have an active Ontario Health Insurance Plan number – must have a valid Canadian Social Insurance Number – Access to wi-fi network and computing device (phone, tablet, computer) Exclusion Criteria:

  • none

Gender Eligibility: All

Female based on self-representation of gender identity

Minimum Age: 18 Years

Maximum Age: 49 Years

Are Healthy Volunteers Accepted: No

Investigator Details

  • Lead Sponsor
    • Royal Victoria Hospital, Canada
  • Provider of Information About this Clinical Study
    • Principal Investigator: Giulio DiDiodato, Chief Research Scientist – Royal Victoria Hospital, Canada
  • Overall Official(s)
    • Giulio DiDiodato, MD PhD, Principal Investigator, Royal Victoria Regional Health Centre
  • Overall Contact(s)
    • Giulio DiDiodato, MD PhD, 7057289090, didiodatog@rvh.on.ca

Clinical trials entries are delivered from the US National Institutes of Health and are not reviewed separately by this site. Please see the identifier information above for retrieving further details from the government database.

At TrialBulletin.com, we keep tabs on over 200,000 clinical trials in the US and abroad, using medical data supplied directly by the US National Institutes of Health. Please see the About and Contact page for details.