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NCT05297539 Clinical Trial

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

Rehabilitation Clinical Trial

— LOARAL 2  

Official title:
Optimization of the Role of Action Observation in the Post-operative Rehabilitation of the Total Knee Prosthesis

Clinical Trial Details — Status: Recruiting

Administrative data
NCT number NCT05297539
Other study ID # 2021-A03000-41
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
Start date June 14, 2022
Est. completion date July 15, 2025

Study information
Verified date January 2024
Source Poitiers University Hospital
Contact Romain DAVID, MD
Phone +33 5 49 44 44 44
Email romain.david@chu-poitiers.fr
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial 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.

Recruitment information / eligibility
Status Recruiting
Enrollment 60
Est. completion date July 15, 2025
Est. primary completion date July 15, 2025
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility 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

Related Conditions & MeSH terms

Intervention

Other:
• Point light display
Visualization of point-light human actions

Locations
Country Name City State
France Centre Hospitalier Universitaire Poitiers Poitiers

Sponsors (1)
Lead Sponsor Collaborator
Poitiers University Hospital

Country where clinical trial is conducted

France, 

Outcome
Type Measure Description Time frame Safety issue
Primary The score obtained on the Western Ontario and McMaster (WOMAC) test at inclusion and at the end of the program. Rehabilitation during 3 weeks
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