Disability Clinical Trial
— MN RETAINOfficial title:
Minnesota Retaining Employment and Talent After Injury/Illness Network (RETAIN) Phase 2
Verified date | April 2024 |
Source | Mayo Clinic |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
This study is a randomized control trial (RCT) to evaluate the impact of RETAIN program expansion and services on workforce retention and reduction of future workplace disability in the state of MN. The program is funded by US Department of Labor (US DOL) and sponsored jointly with the US Social Security Administration. There will be collaboration between partners to implement best practices in early intervention to support injured or ill employees in stay-at-work and return-to-work. MN RETAIN involves a partnership between Mayo Clinic and MN Department of Employment and Economic Development (DEED), MN Department of Labor and Industry (DLI), MN Department of Health (MDH), Workforce Development, Inc. (WDI), and the Governor's Workforce Development Board. MN DEED serves as the main recipient and administrator of the funding within the state with Mayo Clinic, DLI, and WDI, as subrecipients of the grant.
Status | Active, not recruiting |
Enrollment | 3200 |
Est. completion date | May 2025 |
Est. primary completion date | May 2025 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years and older |
Eligibility | Inclusion Criteria: - > 18 years old - MN resident - Works in MN - Employed or currently in the labor force - Has worked at least one day within the last 3 months (80% or more of participants) - Has worked at least one day greater than 3 months but less than 6 months prior (up to 20% of participants) - Meets one of the following: - Diagnosis of a work related or personal injury or illness that impacts employment - Invasive procedure (e.g., surgery) within the past 12-weeks or anticipated within the next 8-weeks that impacts employment Exclusion Criteria: - Legal representation/litigation at the time of enrollment related to the medical condition. - Does not have the capacity to give appropriate informed consent - Employed by a RETAIN healthcare recipient or subrecipient with an existing return-to-work program for employees (i.e. Mayo Clinic employees) - Worker's compensation recipients that have a qualified rehabilitation consultant (QRC) or a disability case manager (DCM) - Pending application or receiving of Social Security Disability Insurance (SSDI) or Supplemental Security Income (SSI) |
Country | Name | City | State |
---|---|---|---|
United States | Mayo Clinic Rochester | Rochester | Minnesota |
Lead Sponsor | Collaborator |
---|---|
Mayo Clinic | Mathematica Policy Research, Minnesota Department of Employment and Economic Development, Minnesota Department of Health, Minnesota Department of Labor and Industry, United States Department of Labor, United States Social Security Administration, Workforce Development, Inc. |
United States,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Workers to maintain employment | Total number of workers employed at the time of program completion and who have maintained employment 12 months after enrollment. | 12 months | |
Primary | Reduction on work disability at 1 years | Total number of enrollees that applied for SSDI or SSI during any of the 1 year after enrollment. | 1 year | |
Primary | Reduction in long term work disability | Total number of enrollees that applied for SSDI or SSI during any of the 5 year after enrollment. | 5 years |
Status | Clinical Trial | Phase | |
---|---|---|---|
Completed |
NCT00906152 -
Association Between Low Back Pain and Quality of Sleep
|
N/A | |
Completed |
NCT00907049 -
Association Between Neck Pain and Quality of Sleep
|
N/A | |
Recruiting |
NCT05394363 -
Generation Victoria Cohort 2020s: A Statewide Longitudinal Cohort Study of Victorian Children and Their Parents
|
||
Recruiting |
NCT05167981 -
RETAINWORKS Impact Evaluation
|
N/A | |
Completed |
NCT01736644 -
Bipolar Sealer Aquamantys Use in Total Knee Replacement
|
N/A | |
Completed |
NCT01407913 -
Caudal Epidural Steroid Injections for Low Back Pain/Sciatic Lumbar Pain
|
Phase 4 | |
Enrolling by invitation |
NCT05173350 -
RETAIN Kentucky Impact Evaluation
|
N/A | |
Completed |
NCT04571827 -
The Influence of Expectations on Post-needling Soreness and Pain Processing After Dry Needling Treatment
|
N/A | |
Recruiting |
NCT03898362 -
Pneumatic Technology for Powered Mobility Devices
|
N/A | |
Completed |
NCT02192658 -
Disability and HIV: Vulnerability of People With Disabilities to HIV Infection in Sub-Saharan Africa
|
N/A | |
Completed |
NCT01600547 -
Odense Fallers and Osteoporosis Study
|
N/A | |
Completed |
NCT00526994 -
Randomized Controlled Trial of Routine Screening for IPV
|
Phase 2/Phase 3 | |
Completed |
NCT00278096 -
Randomised Controlled Trial of Unsolicited Occupational Therapy in Community-Dwelling Elderly
|
N/A | |
Not yet recruiting |
NCT06190041 -
Kinesiophobia in Patients With Chronic Low Back Pain
|
||
Recruiting |
NCT05611723 -
Study and Analysis of Biomechanical Parameters of Human Movement Based on Disability Indicators in Older Adults
|
||
Recruiting |
NCT05656690 -
Prospective Study and Analysis of Biomechanical Parameters of Human Movement Based on Disability Indicators in Older Adults
|
||
Recruiting |
NCT05821140 -
Orofacial Functions and Masticatory Function in Children With Different Types of Deterioration in Oral Health
|
N/A | |
Completed |
NCT02263716 -
Actigraphy to MEasuRe Intensive Care Unit Activity
|
N/A | |
Recruiting |
NCT03408522 -
Troponin Elevation After Major Noncardiac Surgery 2
|
||
Completed |
NCT01241071 -
Effects of Myofascial Release on Pain, Disability and Electromyography of Erector Spinae in Chronic Low Back Pain
|
N/A |