Clinical Trials Directory

Trials / Completed

CompletedNCT03454256

Virtual Reality Rehabilitation in Patients With Total Knee Replacement

Effects of Virtual Reality Rehabilitation in Patients With Total Knee Replacement

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
48 (actual)
Sponsor
IRCCS San Raffaele Roma · Academic / Other
Sex
All
Age
50 Years – 80 Years
Healthy volunteers
Not accepted

Summary

Impaired proprioceptive accuracy could be a risk factor for progression of gait limitations in knee osteoarthritis patients, even after the Total Knee Replacement (TKR). Recent studies on Virtual Reality (VR) in rehabilitation show its efficacy in restoring proprioceptive capacity, postural control and gait. However, literature lacks such studies in TKR patients. This preliminary study aims to evaluate the efficacy of a VR system for the enhancement of motor skills in TKR patients compared to a traditional approach of rehabilitation.

Detailed description

In this randomized controlled trial (RCT), the randomization of the sample will be performed by a local software and in a single blind design. Forty patients will be enrolled and after giving the informed consent, assigned to two groups : * the experimental group (VRG), which will be undergone to treatment with virtual reality for the recovery of load distribution and proper gait pattern; * the control group (CG), which will be undergone to a traditional rehabilitation addressed to recovery of correct gait pattern for the same time period as VRG. Both treatments consist in 15 sessions, at least 5 per week , each lasting 45 minutes. Both VRG or CG will last for 21 days from the start of treatment. All patients, in adjunction to Virtual Reality Rehabilitation (EG) or Traditional Rehabilitation (CG), will execute a global rehabilitation project, consisting in Physiotherapy, Physical Therapies for pain and inflammation control, and Occupational Therapy, personalized by a multidisciplinary rehabilitation team for a minimum of 150-180 minutes per day, and according to their clinical conditions for them. The purposes of this study in detail are: 1. Observing differences in the distribution of the bi-podalic load in the group that performs a re-education with virtual reality compared to those who perform the traditional treatment. 2. Observing differences in the recovery time of a correct pattern of gait in the group that performs a re-education with virtual reality compared to those who perform a traditional treatment. 3. Observing changes in neurophysiological patterns in the two groups.

Conditions

Interventions

TypeNameDescription
DEVICEVirtual RealityVirtual Reality Rehabilitation System

Timeline

Start date
2016-11-08
Primary completion
2019-10-08
Completion
2019-11-13
First posted
2018-03-05
Last updated
2024-04-10

Locations

1 site across 1 country: Italy

Source: ClinicalTrials.gov record NCT03454256. Inclusion in this directory is not an endorsement.