Efficacy of the Individual Placement and Support (IPS) Model
Primary Purpose
Substance Use Disorders
Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Individual Placement and Support Model
Sponsored by
About this trial
This is an interventional treatment trial for Substance Use Disorders focused on measuring employment, disabilities
Eligibility Criteria
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.
Sites / Locations
- CAM
Arms of the Study
Arm 1
Arm Type
Experimental
Arm Label
supported employment
Arm Description
Study consists of one experimental group and one control group. The intervention group received IPS
Outcomes
Primary Outcome Measures
Competitive employment
Secondary Outcome Measures
life satisfaction, job satisfaction, self-esteem, substance and alcohol use
Full Information
NCT ID
NCT01048346
First Posted
January 12, 2010
Last Updated
March 14, 2022
Sponsor
Wright State University
Collaborators
Ohio State University
1. Study Identification
Unique Protocol Identification Number
NCT01048346
Brief Title
Efficacy of the Individual Placement and Support (IPS) Model
Official Title
Efficacy of the Individual Placement and Support (IPS) Model for Consumers With Disability and Substance Use Disorders
Study Type
Interventional
2. Study Status
Record Verification Date
March 2022
Overall Recruitment Status
Completed
Study Start Date
December 1, 2004 (Actual)
Primary Completion Date
May 1, 2009 (Actual)
Study Completion Date
May 1, 2009 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Wright State University
Collaborators
Ohio State University
4. Oversight
Data Monitoring Committee
Yes
5. Study Description
Brief 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.
Detailed 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.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Substance Use Disorders
Keywords
employment, disabilities
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
InvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
223 (Actual)
8. Arms, Groups, and Interventions
Arm Title
supported employment
Arm Type
Experimental
Arm Description
Study consists of one experimental group and one control group. The intervention group received IPS
Intervention Type
Behavioral
Intervention Name(s)
Individual Placement and Support Model
Other Intervention Name(s)
Supported employment intervention
Intervention Description
Psychosocial intervention involving an employment specialist working with participants recruited into the study and assisting with employment.
Primary Outcome Measure Information:
Title
Competitive employment
Time Frame
May 2005 - May 2009
Secondary Outcome Measure Information:
Title
life satisfaction, job satisfaction, self-esteem, substance and alcohol use
Time Frame
May 2005 - May 2009
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
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.
Facility Information:
Facility Name
CAM
City
Dayton
State/Province
Ohio
ZIP/Postal Code
42450
Country
United States
12. IPD Sharing Statement
Learn more about this trial
Efficacy of the Individual Placement and Support (IPS) Model
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