Efficacy of the Individual Placement and Support (IPS) Model

Substance Use Disorders Clinical Trial

Official title:

Efficacy of the Individual Placement and Support (IPS) Model for Consumers With Disability and Substance Use Disorders

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT01048346
• Other study ID #: 0001
• Status: Completed
• Phase: N/A
• Start date: December 1, 2004
• Est. completion date: May 1, 2009

Study information

• Verified date: March 2022
• Source: Wright State University
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

Hypothesis 1. Consumers with disabilities and co-occurring SUD receiving IPS will be more likely to be competitively employed (defined as 1 or more days of work over the past 30 days) at 3, 6 and 12 months following the initiation of vocational treatment goals when compared to a group receiving standard services.

Hypothesis 2. Consumers with disabilities and co-occurring SUD receiving IPS when compared to the comparison group will 1.) be more successful in achieving their employment goals as indicated by the ratio of hours worked to desired hours worked; 2.) become competitively employed sooner; 3.) earn higher wages, 4.) have greater job satisfaction, 5.) have greater economic satisfaction; 6.) have greater life satisfaction, 7.) have greater self-esteem, and 8.) have fewer days of using substances during follow-up points.

Description:

Hypothesis 1. Consumers with disabilities and co-occurring SUD receiving IPS will be more likely to be competitively employed (defined as 1 or more days of work over the past 30 days) at 3, 6 and 12 months following the initiation of vocational treatment goals when compared to a group receiving standard services.

Hypothesis 2. Consumers with disabilities and co-occurring SUD receiving IPS when compared to the comparison group will 1.) be more successful in achieving their employment goals as indicated by the ratio of hours worked to desired hours worked; 2.) become competitively employed sooner; 3.) earn higher wages, 4.) have greater job satisfaction, 5.) have greater economic satisfaction; 6.) have greater life satisfaction, 7.) have greater self-esteem, and 8.) have fewer days of using substances during follow-up points.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 223
• Est. completion date: May 1, 2009
• Est. primary completion date: May 1, 2009
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: All
• Age group: 18 Years to 65 Years

Eligibility

Inclusion Criteria:

• Inclusion criteria includes consumers who are between the ages of 18-65, able to provide informed consent for participation, and are initiating an employment goal in their treatment plan.

Exclusion Criteria:

• Exclusion criteria includes anyone who is currently employed and has been for the past 30 days, have an open case with the Ohio Rehabilitation Services Commission, or have an open case with another vocational rehabilitation provider.

Related Conditions & MeSH terms

• Substance Use Disorders
• Substance-Related Disorders

Intervention

Behavioral:
• Individual Placement and Support Model
Psychosocial intervention involving an employment specialist working with participants recruited into the study and assisting with employment.

Locations

Country	Name	City	State
United States	CAM	Dayton	Ohio

Sponsors (2)

Lead Sponsor	Collaborator
Wright State University	Ohio State University

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Competitive employment		May 2005 - May 2009
Secondary	life satisfaction, job satisfaction, self-esteem, substance and alcohol use		May 2005 - May 2009