Benefits of Observing Point-light Displays in Postoperative Rehabilitation of the Total Knee Prosthesis.

NCT ID: NCT03856983

Last Updated: 2021-09-29

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

36 participants

Study Classification

INTERVENTIONAL

Study Start Date

2020-01-14

Study Completion Date

2021-06-25

Brief Summary

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The LOARAL project concerns patients who have undergone total knee arthroplasty to treat symptomatic osteoarthritis. Patient will be divided into two groups: a control group where patients will do standard rehabilitation and an experimental group where patients will do standard rehabilitation associated with the judgement of point-light display. The aim of this study is to validate the use of point-light display for the Rehabilitation of patients with a totalarthroplasty of the knee.

Detailed Description

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Conditions

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Knee Surgery Rehabilitation Point Light Display

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

OTHER

Blinding Strategy

NONE

Study Groups

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Control group

Control group who will do usual rehabilitation.

Group Type NO_INTERVENTION

No interventions assigned to this group

Experimental group

Experimental group who will do usual rehabilitation and visualization of point-light human actions

Group Type EXPERIMENTAL

Point light display

Intervention Type OTHER

Experimental group who will do usual rehabilitation and visualization of point-light human actions

Interventions

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Point light display

Experimental group who will do usual rehabilitation and visualization of point-light human actions

Intervention Type OTHER

Eligibility Criteria

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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)
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Poitiers University Hospital

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Locations

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Centre Hospitalier Universitaire

Poitiers, , France

Site Status

Countries

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France

Other Identifiers

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2019-A00450-57

Identifier Type: -

Identifier Source: org_study_id

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