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Not yet recruiting NCT06936267

Benefits of Early Proprioceptive Re-education Without Visual Information After Total Knee Arthroplasty

No phase Interventional Unilateral Primary Osteoarthritis, Left Knee

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: rehabilitation : eyes closed, rehabilitation : eyes open.
Who it may be relevant to
Registry conditions: Unilateral Primary Osteoarthritis, Left Knee. Basic parameters: 60 years — 85 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
France
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →

Overview

Osteoarthritis is a common and disabling joint disease, affecting 4.7% of men and 6.6% of women in France. It causes pain and impaired joint mobility, as well as a reduction in proprioception due to damage to intra-articular mechanoreceptors. In the long term, gonarthrosis can lead to limitations in activities of daily living and increase the risk of falls and institutionalisation. Total knee arthroplasty is an effective treatment for reducing pain and improving functional capacity. However, 50% of patients operated on are not satisfied with the results obtained at 6 months, and between 37% and 55% experience no significant improvement in their functional mobility. It is therefore important to better define the modalities of rehabilitation interventions in order to improve their efficiency and the functional benefits for the patient. Proprioception, the visual system and the vestibular system are the three major systems involved in posture and balance. Rehabilitation interventions aimed at improving balance involve these three inputs and their interaction. Studies have shown that proprioceptive rehabilitation can significantly improve balance and gait in patients who have undergone total knee arthroplasty. However, visual feedback may hinder the development of balance skills by limiting the use of other sensorimotor systems.

Detailed description

The aim of this research project is to determine the benefits of visual deprivation and the methods of early proprioceptive exercises, right from the start of rehabilitation, on postural control in patients following total knee arthroplasty. Proprioceptive re-education with the eyes closed will be used from the very first rehabilitation sessions, evaluating its effect on proprioception. Currently, only one study has looked at the influence of the visual system in proprioceptive rehabilitation after total knee arthroplasty, seeking to assess the superiority of exercises with visual feedback compared with exercises without such feedback. The investigator presents an opposite and innovative questioning by proposing to evaluate on a larger scale the influence of visual deprivation rather than visual feedback.

Interventions

  • Other rehabilitation : eyes closed
    proprioceptive exercise with eyes closed
  • Other rehabilitation : eyes open
    proprioceptive exercise with eyes open

Primary outcome measures

  • the length of the projection of the centre of gravity on a posturography platform, in bipedal support, eyes closed, over 30 seconds [Time frame: 3 weeks after randomization]

Eligibility criteria

Inclusion criteria

  • Patient aged between 60 and 85 having undergone primary total knee arthroplasty for gonarthrosis
  • Patient admitted to a Continuing Care and Rehabilitation (CCR) department and having received a maximum of 1 functional re-education session
  • Patient able to remain in bipodal support with eyes closed for 30 seconds on inclusion
  • Weight below the limit accepted by the posturography platform (100 kg)
  • Patient having read and understood the information letter and having signed the consent form
  • Affiliation with the social security system

Exclusion criteria

  • Blindness
  • Diabetes with peripheral neuropathy
  • Central or peripheral nerve pathology (cerebellar syndrome, stroke sequelae, etc.)
  • Previously known ataxia
  • Alcoholism not withdrawn
  • Pre-existing gait disorders making assessment impossible
  • Disorders of the vestibular system
  • Inflammatory rheumatism
  • Length of stay in surgery > 7 days
  • Person deprived of liberty by administrative or judicial decision or person placed under court protection / sub-guardianship or guardianship

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Allocation
Randomized
Model
Parallel assignment
Masking
Single blind
Primary purpose
Other

Study locations

France · 2 centers
  • CRMPR - les herbiers — Bois-Guillaume
  • Chu Rouen — Rouen

Identifiers

NCT: NCT06936267 · 2019/072/HP

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗