Pathways to Vocational Rehabilitation: Enhancing Entry and Retention
1 other identifier
interventional
200
1 country
1
Brief Summary
This study will examine the barriers and supports for entering and receiving work-related services for veterans with a serious mental illness. It will also determine the effectiveness of a brief motivational interviewing intervention designed to help veterans receive these services.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for not_applicable
Started Mar 2005
Typical duration for not_applicable
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
March 1, 2005
CompletedFirst Submitted
Initial submission to the registry
September 14, 2005
CompletedFirst Posted
Study publicly available on registry
September 22, 2005
CompletedPrimary Completion
Last participant's last visit for primary outcome
January 1, 2007
CompletedStudy Completion
Last participant's last visit for all outcomes
September 1, 2007
CompletedMarch 14, 2008
March 1, 2008
1.8 years
September 14, 2005
March 11, 2008
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Entry and Retention in Vocational Rehabilitation
18 months post intervention
Study Arms (1)
1
OTHERSingle session orientation to available services
Interventions
Eligibility Criteria
You may qualify if:
- Current diagnosis of serious mental illness, present for at least 2 years
- Is unemployed or underemployed
- Current episode of un/underemployment is at least 3 months
- Enrolled to receive services at study site
You may not qualify if:
- Over the age of 55
- Non-English speaker
- Mini-Mental score of less than 20
- Planning to move more than 30 miles from study site in the next 18 months
- Previously screened for this study
- Currently or previously involved in other research studies which may impact variables relevant to this study
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Edith Nourse Rogers Memorial Veterans Hospital, Bedford
Bedford, Massachusetts, 01730, United States
Study Officials
- PRINCIPAL INVESTIGATOR
Charles Drebing, PhD
Edith Nourse Rogers Memorial Veterans Hospital, Bedford
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- SINGLE
- Who Masked
- OUTCOMES ASSESSOR
- Purpose
- TREATMENT
- Intervention Model
- SINGLE GROUP
- Sponsor Type
- FED
Study Record Dates
First Submitted
September 14, 2005
First Posted
September 22, 2005
Study Start
March 1, 2005
Primary Completion
January 1, 2007
Study Completion
September 1, 2007
Last Updated
March 14, 2008
Record last verified: 2008-03