- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT01387100
A Modified Rehabilitation Intervention for Working Persons With Arthritis (Work It)
February 20, 2015 updated by: Boston University
Efficacy of a Modified Vocational Rehabilitation Intervention for Work Disability
The purpose of this study is to explore the effects of a brief vocational rehabilitation intervention on individuals with arthritis who are concerned about their ability to remain employed.
Study Overview
Status
Unknown
Conditions
Intervention / Treatment
Study Type
Interventional
Enrollment (Anticipated)
300
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
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Massachusetts
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Boston, Massachusetts, United States, 02215
- Boston University, Sargent College of Health and Rehabilitation Sciences
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
25 years to 63 years (Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Description
Inclusion Criteria:
- Live or work in eastern Massachusetts
- Age 25-63 years
- Risk of work loss due to arthritis
- Arthritis
- Chronic back pain
- Currently employed
Exclusion Criteria:
- Unemployed
- No arthritis
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Supportive Care
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Experimental: Physical Therapist/Occupational Therapist Intervention
This group will be assigned a physical therapist or occupational therapist to meet with followed by 2 phone consultations.
|
Physical or occupational therapist will deliver a vocational rehabilitation intervention using the Work Experience Survey for Persons with Rheumatic Conditions (WES-RC) assessment tool to assess subject's health and vocational background as well as work barriers.
|
No Intervention: Control
This is the control group.
This group will not receive the vocational rehabilitation intervention from an occupational or physical therapist.
They will receive written information regarding job accommodations and disability advocacy.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Change in work status
Time Frame: Baseline, 6, 12, 24 month follow up
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Work limitation will be assessed using the Work Limitation Questionnaire, a tool developed to assess limitation in ability to work due to health.
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Baseline, 6, 12, 24 month follow up
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Collaborators
Investigators
- Principal Investigator: Julie Keysor, PhD, Boston University
Publications and helpful links
The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.
General Publications
- AlHeresh R, Vaughan MW, Brenner IH, Keysor J. Recruitment cost and outcomes for an arthritis work disability prevention randomized clinical trial: The Work It study. Contemp Clin Trials Commun. 2021 Nov 12;24:100862. doi: 10.1016/j.conctc.2021.100862. eCollection 2021 Dec.
- Keysor JJ, LaValley MP, Brown C, Felson DT, AlHeresh RA, Vaughan MW, Yood R, Reed JI, Allaire SJ. Efficacy of a Work Disability Prevention Program for People with Rheumatic and Musculoskeletal Conditions: A Single-Blind Parallel-Arm Randomized Controlled Trial. Arthritis Care Res (Hoboken). 2018 Jul;70(7):1022-1029. doi: 10.1002/acr.23423. Epub 2018 Apr 25.
Helpful Links
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start
June 1, 2011
Primary Completion (Anticipated)
December 1, 2015
Study Completion (Anticipated)
March 1, 2016
Study Registration Dates
First Submitted
June 23, 2011
First Submitted That Met QC Criteria
July 1, 2011
First Posted (Estimate)
July 4, 2011
Study Record Updates
Last Update Posted (Estimate)
February 23, 2015
Last Update Submitted That Met QC Criteria
February 20, 2015
Last Verified
February 1, 2015
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- H133B100003-1
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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