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IPS/Peer Support Intervention in the DTES

Optimizing the Employment Outcomes for People Living in the Downtown Eastside

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03748004
Enrollment
72
Registered
2018-11-20
Start date
2018-11-14
Completion date
2020-05-01
Last updated
2019-06-17

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Behavior, Adaptive, Mental Illness, Substance Use

Keywords

Homeless, Employment

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.

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.

Interventions

BEHAVIORALIPS/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

BEHAVIORALWorkBC

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.

Sponsors

Ministry of Social Development and Poverty Reduction, British Columbia
CollaboratorOTHER
University of British Columbia
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
OTHER
Masking
SINGLE (Investigator)

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).

Eligibility

Sex/Gender
ALL
Age
19 Years to No maximum
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

Design outcomes

Primary

MeasureTime frameDescription
Securing employment18 monthsRC will follow-up with all recruited clients who get employed through the IPS/Peer Support intervention and the WorkBC control group.

Secondary

MeasureTime frameDescription
PHQ-9 Questionnaire to measures level of depression18 monthsParticipants 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
GAD7 questionnaire to measure general anxiety disorder18 monthsParticipants 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.
C-PROM questionnaire to measure Personal Recovery18 monthsParticipants 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
REQOL questionnaire measures Recovery Quality of Life18 monthsParticipants 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.
SWL questionnaire measures satisfaction with life18 monthsParticipants 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.

Countries

Canada

Contacts

Primary ContactSkye Barbic, PhD
skye.barbic@ubc.ca778 846 6134

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026