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Prevention, Management and Rehabilitation of Knee Osteoarthritis at the Workplace

N

National Research Centre for the Working Environment, Denmark

Status

Not yet enrolling

Conditions

Knee Pain Chronic
Knee Osteoarthritis
Knee Discomfort

Treatments

Behavioral: Blood flow restriction (BFR)
Behavioral: Usual care (control)

Study type

Interventional

Funder types

Other

Identifiers

NCT05822401
10429
H-22016339 (Other Identifier)

Details and patient eligibility

About

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.

Enrollment

80 estimated patients

Sex

All

Ages

18 to 67 years old

Volunteers

Accepts Healthy Volunteers

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

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

80 participants in 2 patient groups

Blood flow restriction (BFR)
Experimental group
Description:
Blood flow restricted training (BFR) integrated into the daily work tasks for 8 weeks.
Treatment:
Behavioral: Usual care (control)
Behavioral: Blood flow restriction (BFR)
Usual care (control)
Active Comparator group
Description:
Will continue their work as usual
Treatment:
Behavioral: Usual care (control)

Trial contacts and locations

0

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Central trial contact

Sebastian Skovlund

Data sourced from clinicaltrials.gov

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