Optimization of the Role of Action Observation in the Post-operative Rehabilitation of the Total Knee Prosthesis: (LOARAL 2)

Not Applicable

Completed

• Conditions: Knee Surgery; Point Light Display; Rehabilitation

• Registration Number: NCT05297539
• Lead Sponsor: Poitiers University Hospital

Brief Summary

The LOARAL 2 project concerns patients who have undergone total knee arthroplasty to treat symptomatic osteoarthritis. Patient will be divided into three groups: a control group where patients will do standard rehabilitation associated with the judgments of videos represented non-human action and two experimental groups where patients will do standard rehabilitation associated with the judgement of human point-light display. The aim of this study is to measure the benefits of attentional focus and sex correspondence in the use of point-light display for the rehabilitation of patients with a total arthroplasty of the knee.

Detailed Description

Not available

Study Timeline

• Study First Submitted: 2022-03-17
• Study First Submitted QC: 2022-03-25
• Study First Posted: 2022-03-28
• Study Start: 2022-06-14
• Primary Completion: 2024-12-06
• Study Completion: 2024-12-06
• Status Verified: 2025-04
• Last Update Submitted: 2025-04-11
• Last Update Posted: 2025-04-16

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 51

Inclusion Criteria

• Volunteers over 18 years of age who have undergone knee surgery

Exclusion Criteria

• Any locomotor condition not due to knee surgery
• Uncorrected visual disturbances
• Comorbidity altering locomotion (history of stroke, neurological condition, inflammatory rheumatism)

Non randomization criteria:

• Cognitive disorders (Mini Mental State Examination <21)
• Depressive disorders (Beck Inventory index> 9)

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Primary Outcome Measures

Name	Time	Method
The score obtained on the Western Ontario and McMaster (WOMAC) test at inclusion and at the end of the program.	Rehabilitation during 3 weeks

Trial Locations

Locations (1)

Centre Hospitalier Universitaire Poitiers; 🇫🇷 Poitiers, France