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

Rehabilitation Clinical Trial

— LOARAL  

Official title:

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

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT03856983
• Other study ID #: 2019-A00450-57
• Status: Completed
• Phase: N/A
• Start date: January 14, 2020
• Est. completion date: June 25, 2021

Study information

• Verified date: September 2021
• Source: Poitiers University Hospital
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

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.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 36
• Est. completion date: June 25, 2021
• Est. primary completion date: June 25, 2021
• 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)

Related Conditions & MeSH terms

• Knee Surgery
• Point Light Display
• Rehabilitation

Intervention

Other:
• Point light display
Experimental group who will do usual rehabilitation and visualization of point-light human actions

Locations

Country	Name	City	State
France	Centre Hospitalier Universitaire	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	Compare the evaluation of the point light display relative to conventional rehabilitation	The time to realize the time up and go test will be assessed at inclusion and at the end of the program.	Rehabilitation during 3 weeks
Secondary	Compare the evaluation of the point light display on functional recovery	Test score the time up and go and test score questionnary WOMAC (Western Ontario and McMaster Universities Osteoarthritis Index, Bellamy et al., 1988).	At the end of the program (3 weeks max)
Secondary	Compare the evaluation of the point light display on the detection and action recognition	Percentages of correct recognition of actions on the point light display	At the end of the program (3 weeks max)
Secondary	Compare the evaluation of the point light display on the feeling of self-efficacy personal	Test score questionnary of self-efficacy personal (Dumont et al., 2000).	At the end of the program (3 weeks max)