Knee Surgery, Point Light Display, Rehabilitation
Conditions
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.
Interventions
OTHERPoint light display
Visualization of point-light human actions
Sponsors
Poitiers University Hospital
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
OTHER
Masking
NONE
Eligibility
Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No
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)
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The score obtained on the Western Ontario and McMaster (WOMAC) test at inclusion and at the end of the program. | Rehabilitation during 3 weeks |
Countries
France
Outcome results
None listed