- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05173350
RETAIN Kentucky Impact Evaluation
One-Year Impact Evaluation of Retaining Employment and Talent After Injury/Illness Network (RETAIN) Kentucky
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
SSA contracted with Mathematica to conduct an independent evaluation of RETAIN Kentucky. Under the RETAIN model medical providers receive training and incentives to use occupational health best practices. The state agency also coordinates SAW/RTW services for the enrollee, fosters communication among RETAIN stakeholders about the treatment enrollee returning to work, and monitors the enrollee's medical and employment progress. RETAIN Kentucky also provides individualized intensive vocational services from RETAIN RTW Coordinators, with an emphasis on assistive technology, universal design, and peer support.
Kentucky uses a multi-method approach toward recruitment that includes referrals from medical providers, employers, Office of Vocational Rehabilitation, workforce and disability management organizations, community partners, and word of mouth. A return-to-work (RTW) coordinator conducts intake, determines enrollees' eligibility, and randomly assigns each enrollee to either a treatment group that is eligible to receive the full set of RETAIN intervention activities or a control group that is not. The evaluation team then compares the outcomes of the two groups and gathers evidence on how each RETAIN project shaped the outcomes of enrollees who were eligible for its services, regardless of whether they participated in those services. Data sources include enrollment data, surveys, administrative records, program data, and qualitative data.
Study Type
Enrollment (Anticipated)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
Kentucky
-
Lexington, Kentucky, United States, 40506
- Human Development Institute, University of Kentucky
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- Individuals who are at risk of exiting the workforce due to non-work-related illness of injury
- Individuals who are employed or have been employed within the last 12 months and made at least $1,000 in one of those months
- Individuals who reside in the Kentucky
- Individuals must not have applied for or be receiving federal disability benefits including SSDI and SSI within the last 5 years
Exclusion Criteria:
- Individuals who are do not have a non-work-related illness or injury that puts them at risk of exiting the workforce
- Individuals who unemployed or have not been employed within the last 12 months
- Individuals who have not made at least $1,000 in the past 12 months
- Individuals who do not reside in the Kentucky
- Individuals who have applied for or be receiving federal disability benefits including SSDI and SSI within the last 5 years
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Health Services Research
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: RETAIN Programming
The experimental group receives the full set of RETAIN intervention activities.
|
The experimental group receives a combination of medical provider services, stay-at-work (SAW)/return-to-work (RTW) coordination services, and other SAW/RTW services.
Services offered by the project include individualized intensive vocational services from RETAIN RTW Coordinators, with an emphasis on assistive technology, universal design, and peer support.
The project provides training on SAW/RTW best practices and RETAIN, as well as financial incentives to health care professionals.
The treatment group is eligible to receive the full set of RETAIN intervention activities.
|
|
Active Comparator: Active Comparator
The active comparator group does not receive the full set of RETAIN intervention activities.
|
Those in the active comparator arm continue to receive medical services.
A RTW coordinator creates a RTW plan with the enrollee and refers them to existing resources.
The RTW coordinator works with enrollees for 2.5 hours total.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Share of enrollees that applied for SSDI or SSI during the 12 months after enrollment
Time Frame: Measured in the 12 months after enrollment
|
Share of enrollees that applied for SSDI or SSI during any of the 12 months after enrollment obtained from SSA program data.
These files include detailed information about Social Security Disability Insurance (SSDI) and Supplemental Security Income (SSI) applications SSDI and SSI awards, SSDI and SSI benefit amounts and enrollee characteristics (for enrollees who have ever applied for SSA program benefits)
|
Measured in the 12 months after enrollment
|
|
Share of enrollees employed in the fourth quarter after enrollment
Time Frame: Measured over the three months in the fourth quarter after enrollment
|
Share of enrollees employed in the fourth quarter after enrollment obtained from state unemployment insurance wage records.
These files include individual-level wage records for six quarters surrounding enrollment in the study, including the quarter prior to enrollment, the quarter of enrollment, and four post-enrollment quarters.
|
Measured over the three months in the fourth quarter after enrollment
|
|
Enrollee earnings in the fourth quarter after enrollment
Time Frame: Measured over the three months in the fourth quarter after enrollment
|
Sum of enrollee earnings in the fourth quarter after enrollment obtained from state unemployment insurance wage records.
These files include individual-level wage records for six quarters surrounding enrollment in the study, including the quarter prior to enrollment, the quarter of enrollment, and four post-enrollment quarters.
|
Measured over the three months in the fourth quarter after enrollment
|
Collaborators and Investigators
Collaborators
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Anticipated)
Study Completion (Anticipated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- RTN-KY
- OD-36364-21-75-4-21 (Other Grant/Funding Number: SSA)
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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.
Clinical Trials on Disability
-
Northwestern Health Sciences UniversityHealth Resources and Services Administration (HRSA)CompletedNeck Disability | Back DisabilityUnited States
-
University of ExtremaduraUniversity of CadizCompletedDisability Physical | Disabilities Multiple | Disability, Intellectual | Disability Hearing | Disability, VisionSpain
-
Amager HospitalLundbeck FoundationCompletedHip Disability | Groin DisabilityDenmark
-
Mathematica Policy Research, Inc.Social Security AdministrationCompleted
-
Mathematica Policy Research, Inc.Social Security AdministrationCompleted
-
Polytechnic Institute of PortoUniversidade do Porto; School of Allied Health Sciences of Porto (ESTSP) -... and other collaboratorsCompleted
-
University of FloridaWithdrawn
-
GalenusRx, Inc.CP UnlimitedNot yet recruitingDevelopmental Disability | Intellectual Disability, Mild | Intellectual Disability, Mild to ModerateUnited States
-
Second Affiliated Hospital, School of Medicine,...Recruiting
-
VA Office of Research and DevelopmentTerminated
Clinical Trials on RETAIN KY
-
Mayo ClinicU.S. Department of Education; Minnesota Department of Employment and Economic...RecruitingDisability | Injuries Related Work | Illness Related WorkUnited States
-
Mathematica Policy Research, Inc.Minnesota Department of Health; Social Security Administration; Department of... and other collaboratorsRecruiting
-
Kafrelsheikh UniversityCairo UniversityCompletedBone Loss | Implant Site ReactionEgypt
-
Novatim Immune Therapeutics (Zhejiang) Co., Ltd.RecruitingNeoplasms | Neoplasms by Histologic TypeChina
-
Mayo ClinicMinnesota Department of Health; Workforce Development, Inc.; Minnesota Department... and other collaboratorsCompletedDisability | Injuries Related Work | Illness Related WorkUnited States
-
Mathematica Policy Research, Inc.Social Security AdministrationCompleted
-
Mathematica Policy Research, Inc.Social Security AdministrationCompleted
-
Jamie StudtsUniversity of Louisville; Bristol-Myers Squibb Foundation; Lung Cancer AllianceCompletedLung CancerUnited States
-
New York UniversityNational Institute on Drug Abuse (NIDA)Completed
-
USDA Food and Nutrition ServiceMathematica Policy Research, Inc.CompletedFood Insecurity Among Children