Actively Recruiting

Phase Not Applicable
Age: 40Years - 85Years
All Genders
NCT06290336

Pre-Operative Exercise Therapy and Patient Education Before Total Knee Replacement

Led by Linkoeping University · Updated on 2026-02-03

110

Participants Needed

1

Research Sites

200 weeks

Total Duration

On this page

Sponsors

L

Linkoeping University

Lead Sponsor

R

Region Östergötland

Collaborating Sponsor

AI-Summary

What this Trial Is About

The goal of this multi-center randomized controlled trial is to investigate the effect of pre-operative exercise therapy and education for patients awaiting knee replacement surgery on subjective knee function, patient satisfaction and enablement compared to standard care. The main questions it aims to answer are: * Does pre-operative exercise therapy and education lead to better subjective knee function compared to standard care one year after surgery? * Does pre-operative exercise therapy and education lead to a higher level of patient satisfaction compared to standard care one year after surgery? * Does pre-operative exercise therapy and education lead to better patient enablement compared to standard care six weeks after surgery? * Does pre-operative exercise therapy and education lead to better objective knee function compared to standard care six weeks after surgery? Participants will be randomized stratified by age (≤ 67 years, \> 67 years) to either pre-operative supervised individualized exercise therapy combined with education two sessions/week (intervention group) or to standard care (control group). The intervention will be continuously ongoing for at least eight weeks from the point of decision for surgery until as close to the surgery as possible.

CONDITIONS

Official Title

Pre-Operative Exercise Therapy and Patient Education Before Total Knee Replacement

Who Can Participate

Age: 40Years - 85Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Waiting list for primary unilateral knee replacement surgery
  • Osteoarthritis of the knee as the primary reason for surgery
  • Reside within 60 minutes of travel to the site of the intervention
Not Eligible

You will not qualify if you...

  • Previous knee replacement surgery in the other knee
  • Other reasons than osteoarthritis of the knee as the primary reason for surgery
  • Impaired cognitive function
  • Not independently speaking and reading Swedish
  • Chronic illness or disability preventing full participation in the intervention

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Linkoping University

Linköping, Östergötland County, Sweden, 58183

Actively Recruiting

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Research Team

M

Marcus Ljung, PhD-student

CONTACT

J

Joanna Kvist, Professor

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

SINGLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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