Effects of Blood-flow Restricted Exercise Compared to Standard Rehabilitation in Patients With Knee Osteoarthritis

NCT05437770 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 96

Last updated 2025-06-29

No results posted yet for this study

Summary

The purpose of this study is to investigate the effect of low-intensity BFR exercise on joint pain, muscle mass, and mechanical muscle function compared to standard rehabilitering in adults with knee-OA.

Conditions

  • Osteoarthritis, Knee

Interventions

OTHER

BFR (Blood-Flow Restricted exercise)

The BFR group performs unilateral training with the knee-OA diagnosed leg first. BFR exercise is performed with a pneumatic cuff placed at the top of the thigh on the leg being trained. The cuff will be inflated to 60-80 % of the total arterial occlusion pressure (AOP). The participant will afterwards perform training of the knee extensors in a leg press exercise machine and a leg extension exercise machine with a load corresponding to 30 % of the maximal load (1RM = Repetition Maximum).

OTHER

Standard rehabilitation

The GLA:D programme involves a circuit training program with four stations. Each station involves two to six exercises where the participants perform 10-15 repetitions over 2-3 sets, which depends on the participants pain- and functional level. Following the 8 weeks GLA:D programme, participants will continue 4 weeks of team group training performing similar neuromuscular lower limb exercises as for the first 8 weeks.

Sponsors & Collaborators

  • University of Southern Denmark

    collaborator OTHER
  • Gigtforeningen

    collaborator OTHER
  • Sygekassernes Helsefond

    collaborator OTHER
  • AP Moeller Foundation

    collaborator OTHER
  • Aase and Ejnar Danielsens Foundation

    collaborator OTHER
  • Praksisfonen

    collaborator UNKNOWN
  • FAPS

    collaborator UNKNOWN
  • Bispebjerg Hospital

    lead OTHER

Principal Investigators

  • Finn E Johannsen, MD · Institute of Sports Medicine

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Model
PARALLEL

Eligibility

Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2022-01-01
Primary Completion
2025-01-15
Completion
2025-02-14

Countries

  • Denmark

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT05437770 on ClinicalTrials.gov