Supported Employment in a Swedish Context

Phase 2

• Conditions: Psychosis
• Interventions: Behavioral: Individual Placement and Support-vocational rehabilitation; Behavioral: Vocational rehabilitation available

• Registration Number: NCT00960024
• Lead Sponsor: Vardalinstitutet The Swedish Institute for Health Sciences

Brief Summary

This project aims at generating evidence of a work-rehabilitation strategy that benefits the people with severe mental illness (SMI) who want to work, increase their sense of well-being and integration in society, decrease their financial dependence and experiences of stigma and discrimination. The project is likely to help form the basis of how to implement the evidence based supported employment (SE)-model, Individual Placement and Support model (IPS), in a Swedish work-rehabilitation context. In the long run, evidence of SE in a Swedish context could help to decrease the period of sick-leave and increase fulfilling and productive lifestyles among people with severe mental illness. In all, the effectiveness of SE can improve the quality of life for the target group, the quality in mental health care rehabilitation and decrease the costs of treatment and care.

Detailed Description

Evidence-based mental health treatment and scientific support has gained increased attention in Sweden. The Swedish National Board of Health and Welfare emphasizes the importance of Supported Employment. Especially since there are no study in Sweden that has an RCT-design, and that fully take on the responsibility of implementing a SE- intervention in concordance with the evidence based version of SE in mental health care, the Individual Placement and Support model, IPS. Internationally, SE according to IPS is an evidence-based approach to help people with SMI find and keep employment. RCT and quasi-experimental studies showed that IPS (Place-Then-Train), is more effective than the traditional stepwise vocational rehabilitation model(Train-Then-Place. However, there is no research evidence if the SE/IPS will function in relation to a Swedish benefit and health system and work-rehabilitation context. This intervention project will therefore not only study the effects of vocational and health-related outcomes and experiences, but also study the implementation of SE/IPS, its feasibility and level of fidelity in a Swedish context.

Study Timeline

• Study Start: 2008-04
• Status Verified: 2009-08
• Study First Submitted: 2009-08-14
• Study First Submitted QC: 2009-08-14
• Last Update Submitted: 2009-08-14
• Study First Posted: 2009-08-17
• Last Update Posted: 2009-08-17
• Primary Completion: 2011-02
• Study Completion: 2015-12

Recruitment & Eligibility

• Status: UNKNOWN
• Sex: All
• Target Recruitment: 120

Inclusion Criteria

• People with Severe mental illness, which mostly means having a diagnosis of psychosis
• Communicate in Swedish
• Express interest in working in the near future
• Have professional care or support from psychiatric clinic
• Attend to a SE-introductory meeting

Exclusion Criteria

• Additional organic or physical disability to having psychosis

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Arm && Interventions

Group	Intervention	Description
Individual Placement and Support-vocational rehabilitation	Individual Placement and Support-vocational rehabilitation	-
Vocational rehabilitation available at study site	Vocational rehabilitation available	-

Primary Outcome Measures

Name	Time	Method
To determine the effectiveness of SE/IPS in terms of vocational outcomes, such as employment rate, monthly income, job-tenure and working hours compared to stepwise rehabilitation available, for people with SMI in a Swedish context	6 months, 18 months, and 24 months (6 months after end of intervention)

Secondary Outcome Measures

Name	Time	Method
To determine the effectiveness of a SE in terms health-related and functional outcomes, such as symptoms, perceived discrimination, empowerment, work-readiness, self-image, level of social and community participation, and quality of life	6 months, 18 months, and 24 months (6 months after end of intervention)

Trial Locations

Locations (1)

The Vardal Institute, Medical Faculty, Lund University; 🇸🇪 Lund, Sweden