IPS/Peer Support Intervention in the DTES

Sponsor
University of British Columbia (Other)
Overall Status
Unknown status
CT.gov ID
NCT03748004
Collaborator
Ministry of Social Development and Poverty Reduction, British Columbia (Other)
72
3
2
17.5
24
1.4

Study Details

Study Description

Brief Summary

Individual placement support (IPS) is an evidence-based supported employment model for people with severe mental illness, designed to achieve employment in mainstream competitive jobs, either part-time or full-time. The aim of this study is to assess the (i) effectiveness of embedding the (IPS)/Peer Support intervention as part of the primary care centre in securing employment of adults living in the downtown eastside in comparison to the usual treatment WorkBC (control group). (ii) effectiveness of IPS/Peer Support versus the usual treatment (WorkBC) in improving mental illness, quality of life and personal recovery through participation in employment.

Condition or Disease Intervention/Treatment Phase
  • Behavioral: IPS/SP
  • Behavioral: WorkBC
N/A

Detailed Description

This 18-month mixed methods study consists of an effectiveness multi-site randomized controlled trial of the IPS/peer support intervention plus an embedded qualitative exploration of participants' experiences. All clients receiving primary care services from one DTES clinical site who are employment ready and are not receiving mental health services will be randomly assigned to IPS & Peer Support (experimental group) or WorkBC (control group). Clients are required to participate in the intervention for 16 weeks and will be assessed at baseline, 1-, 3-, and 6-months post study intervention start-date for both groups. Assessments will include the 5 questionnaires administered at baseline which cover the following: Employment Quality, Employment Sustainability, Education Quality and Quantity, Quality of Life, Community Engagement and Clinical significant levels of depression and anxiety.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
72 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Intervention Model Description:
72 clients receiving primary care services from one DTES clinical site who are employment ready will be randomly assigned to IPS and Peer Support (experimental group) or WorkBC (control group).72 clients receiving primary care services from one DTES clinical site who are employment ready will be randomly assigned to IPS and Peer Support (experimental group) or WorkBC (control group).
Masking:
Single (Investigator)
Primary Purpose:
Other
Official Title:
Optimizing the Employment Outcomes for People Living in the Downtown Eastside
Actual Study Start Date :
Nov 14, 2018
Anticipated Primary Completion Date :
Nov 30, 2019
Anticipated Study Completion Date :
May 1, 2020

Arms and Interventions

Arm Intervention/Treatment
Experimental: Adults living in the DTES

36 out of the 72 recruited participants who live in the DTES will be randomly assigned to the intervention group (IPS & Peer Support). The IPS and Peer Support will actively work and support with each of the 36 participants in seeking employment and education for 16 weeks. IPS/SP will help participants identify their employment and educational goals, identify potential employers, help prepare their resumes and for interviews, and provide ongoing support during the 16 weeks. 36 out of the 72 participants who live in the DTES will be randomly assigned to the control group (WorkBC). Participants will be provided with WorkBC employment services.

Behavioral: IPS/SP
The 72 recruited clients receiving primary care services from one DTES clinical site who are employment ready will be randomly assigned to IPS and Peer Support (experimental group) or WorkBC control group

Placebo Comparator: Individuals 19 yrs or older settled in DTES

36 out of the 72 recruited participants who live in the DTES will be randomly assigned to the intervention group (IPS & Peer Support). The IPS and Peer Support will actively work and support with each of the 36 participants in seeking employment and education for 16 weeks. IPS/SP will help participants identify their employment and educational goals, identify potential employers, help prepare their resumes and for interviews, and provide ongoing support during the 16 weeks. 36 out of the 72 participants who live in the DTES will be randomly assigned to the control group (WorkBC). Participants will be provided with WorkBC employment services.

Behavioral: WorkBC
36 out of the 72 participants who live in the DTES will be randomly assigned to the control group (WorkBC). Participants will be provided with WorkBC employment services.

Outcome Measures

Primary Outcome Measures

  1. Securing employment [18 months]

    RC will follow-up with all recruited clients who get employed through the IPS/Peer Support intervention and the WorkBC control group.

Secondary Outcome Measures

  1. "PHQ-9" Questionnaire to measures level of depression [18 months]

    Participants will answer the questions on this questionnaire using a likert scale. A scoring system will calculate the final total number and we will assess mean change from the baseline. The minimum score is 0/27 and the maximum score is 27

  2. "GAD7" questionnaire to measure general anxiety disorder [18 months]

    Participants will answer the questions on this questionnaire using a likert scale. A scoring system will calculate the final total number and we will assess mean change from the baseline. The minimum score is 0/21. The maximum score is 21.

  3. "C-PROM" questionnaire to measure Personal Recovery [18 months]

    Participants will answer the questions on this questionnaire using a likert scale. A scoring system will calculate the final total number and we will assess mean change from the baseline. Minimum score is 0/120. Maximum score is 120

  4. "REQOL" questionnaire measures Recovery Quality of Life [18 months]

    Participants will answer the questions on this questionnaire using a likert scale. A scoring system will calculate the final total number and we will assess mean change from the baseline. Minimum score is 0/64. Maximum score 64.

  5. "SWL" questionnaire measures satisfaction with life [18 months]

    Participants will answer the questions on this questionnaire using a likert scale. A scoring system will calculate the final total number and we will assess mean change from the baseline. Minimum score is 5/35. Maximum score is 35.

Eligibility Criteria

Criteria

Ages Eligible for Study:
19 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
  • Adults, age 19 and over, accessing primary care services at the primary care centre listed in this study (CH Pender Community Health Centre)

  • At least one visit to VCH Pender Community Health Centre

  • Currently unemployed and not in school or post-secondary training.

  • Able to provide informed consent and fluent in English (intervention is currently offered in English only).

  • Not hospitalized at the time of recruitment.

Exclusion Criteria:

• Adults, age 19 and over who have access to mental health services

Contacts and Locations

Locations

Site City State Country Postal Code
1 Downtown Community Health Center Vancouver British Columbia Canada V6A 1G9
2 Heatley Community Health Clinic Vancouver British Columbia Canada V6A 3G3
3 Pender Community Health Clinic Vancouver British Columbia Canada V6B 1R3

Sponsors and Collaborators

  • University of British Columbia
  • Ministry of Social Development and Poverty Reduction, British Columbia

Investigators

  • Principal Investigator: Skye Barbic, PhD, University of British Columbia

Study Documents (Full-Text)

None provided.

More Information

Publications

Responsible Party:
Skye Barbic, Assistant Professor, University of British Columbia
ClinicalTrials.gov Identifier:
NCT03748004
Other Study ID Numbers:
  • H18-02740
First Posted:
Nov 20, 2018
Last Update Posted:
Jun 17, 2019
Last Verified:
Jun 1, 2019
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Skye Barbic, Assistant Professor, University of British Columbia
Additional relevant MeSH terms:

Study Results

No Results Posted as of Jun 17, 2019