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Clinical Trials/NCT05822401
NCT05822401Not yet recruitingNot Applicable

Prevention, Management and Rehabilitation of Knee Osteoarthritis at the Workplace

National Research Centre for the Working Environment, Denmark0 sites80 target enrollmentStarted: April 11, 2023Last updated:
Conditions

Trial Snapshot

Phase
Not Applicable
Status
Not yet recruiting
Sponsor
Enrollment
80
Primary Endpoint
Pain intensity

Study Overview

Brief Summary

The goal of this intervention study is to assess the effect of blood flow restricted (BFR) exercise integrated into the daily work tasks among hospital workers with or at increased risk of chronic knee pain.

The main questions are:

Can BFR exercise integrated into the daily work tasks reduce knee pain (primary outcome) and improve function and work ability among hospital workers with or at increased risk of chronic knee pain? Participants in the intervention group will for shorts bouts during their workdays integrate BFR into their daily work tasks involving walking, whereas the control group will continue as usual.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Treatment
Masking
Single (Outcomes Assessor)

Eligibility Criteria

Ages
18 Years to 67 Years (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
Yes

Inclusion Criteria

  • Hospital workers working at least 20 hours per week with or without chronic knee pain (>3 months)

Exclusion Criteria

  • Life-threatening disease
  • Conditions where BFR training may be contraindicated, e.g. pregnancy, cancer, diabetes, major cardiovascular disease, current, previous or family history of clotting disorders, recent immobilization, major surgery or injections into the joint (i.e. corticosteroid injection)
  • Systolic/diastolic blood pressure above 160/100 mmHg

Outcomes

Primary Outcomes

Pain intensity

Time Frame: Change pre-post 8 weeks of intervention

Change in worst knee pain intensity during the last week rated on a 11-point numeric rating scale (NRS)

Secondary Outcomes

  • Functional performance(Change pre-post 8 weeks of intervention)
  • Work ability(Change pre-post 8 weeks of intervention)

Investigators

Sponsor
National Research Centre for the Working Environment, Denmark
Sponsor Class
Other Gov
Responsible Party
Principal Investigator
Principal Investigator

Lars L. Andersen

Professor

National Research Centre for the Working Environment, Denmark

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