- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT00530985
Preserving Function Among Disability Applicants
Preserving Function Among Disability Applicants: A Motivational Enhancement Approach to Benefits Counseling
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
The aim is to develop and test the efficacy of Benefits Counseling to improve quality of life among veterans who apply for VA benefits. Benefits Counseling involves providing claimants information about rehabilitation and work-related activities, benefits determination and management, and available substance abuse treatment . Benefits Counseling is designed to increase motivation to be active and promote engagement in substance abuse treatment. After enrolling 15 participants in an open-label pilot phase, 300 veterans who are not receiving benefits and are applying to VBA for disability benefits will be randomly assigned to Benefits Counseling or the control condition, VA Orientation, and both groups will be followed for one year.
The primary outcome measures will be observer-rated and self-rated quality of life. Secondary outcome measures will include substance use and treatment utilization.
Study Type
Enrollment (Anticipated)
Phase
- Phase 1
Contacts and Locations
Study Locations
-
-
Connecticut
-
West Haven, Connecticut, United States, 06516
- VA Connecticut Health Care System (West Haven)
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- Applying for VA service connection and not currently receiving VBA benefits.
- Veterans who have been rated 0% service-connected but do not receive financial benefits are eligible to participate.
- Able to provide valid consent
- Age 18-65
- Expresses willingness to discuss benefits with a counselor
- Anticipates difficulty working
Exclusion Criteria:
- Already receiving VA payments
- Already receiving SSI or SSDI
- Has a conservator
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: 1
Benefits Counseling
|
Help deciding whether to work
|
|
Active Comparator: 2
VA Orientation
|
Orientation to services available at VA
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
|
Days engaged in work and work-related activities
Time Frame: 6 months
|
6 months
|
Secondary Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
|
substance use (as measured by days having used illicit drugs, alcohol to intoxication in the preceding days)
Time Frame: 6 months
|
6 months
|
|
treatment utilization (days in last 30 having participated in rehabilitation and work-related activities, number of days having participated in non-inpatient substance abuse treatment, number of days on any inpatient unit)
Time Frame: 6 months
|
6 months
|
Collaborators and Investigators
Investigators
- Principal Investigator: Marc I. Rosen, MD, VA Connecticut Health Care System (West Haven)
Study record dates
Study Major Dates
Study Start
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Estimate)
Study Record Updates
Last Update Posted (Estimate)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Other Study ID Numbers
- MR0024
- MIRECC
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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