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

P

Poitiers University Hospital

Status

Completed

Conditions

Point Light Display
Rehabilitation
Knee Surgery

Treatments

Other: Point light display

Study type

Interventional

Funder types

Other

Identifiers

NCT03856983
2019-A00450-57

Details and patient eligibility

About

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.

Enrollment

36 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

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)

Trial design

Primary purpose

Other

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

36 participants in 2 patient groups

Control group
No Intervention group
Description:
Control group who will do usual rehabilitation.
Experimental group
Experimental group
Description:
Experimental group who will do usual rehabilitation and visualization of point-light human actions
Treatment:
Other: Point light display

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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