Knee Osteoarthritis Clinical Trial
— HYDROKNEERVANAOfficial title:
Rehabilitation of Patients With Total Knee Replacement Through the Immersive Virtual Reality in Aquatic Scenarios
Verified date | April 2024 |
Source | IRCCS San Raffaele Roma |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
This study is a multicenter non-randomized single-blind controlled trial, aimed at investigating the feasibility and efficacy of hydrotherapy based on IVR, for the patients with TKR(Total Knee Replacement), on the function, gait performance, postural balance control, and knee edema reduction. The protocol was draft according to the Consolidated Standards of Reporting Trials (CONSORT ) checklists. A total of 96patients with total knee prosthesis will be recruited and divided into three groups, to receive a traditional rehabilitation (TR) program, traditional hydrotherapy (TH)or hydrotherapy through immersive virtual reality (HIVR) using Bts-Nirvana. Assessments will be performed at baseline and at the end of treatment.
Status | Active, not recruiting |
Enrollment | 96 |
Est. completion date | December 30, 2024 |
Est. primary completion date | July 30, 2024 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years to 85 Years |
Eligibility | The inclusion criteria are: - Aged = 85; - Capacity to consent and to perform the exercises of the specific protocol; - Patients with total knee prosthesis. The exclusion criteria are: - Failure to meet the inclusion criteria; - Concomitant participation in other studies; - Unicompartmental knee prostheses; - Surgery without drainage; - Wound complications; - Cognitive disorders; - Diagnosis of epilepsy; - Lack of written informed consent; |
Country | Name | City | State |
---|---|---|---|
Italy | IRCCS San Raffele | Rome | RM |
Lead Sponsor | Collaborator |
---|---|
IRCCS San Raffaele Roma | Istituto Nazionale di Ricovero e Cura per Anziani |
Italy,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Changes in Time Up & Go Test | Time Up and Go test (TUG): TUG is a test used to determine fall risk and measure the progress of balance, sit to stand and walking. The patient starts in a seated position, then stands up, walks 3 meters, turns around, walks back to the chair and sits down. If a patient took 14 seconds or longer to perform the test he was classified as high-risk for falling | At baseline (day 1-T1) and at the end (day 21 -T2) of the treatment. | |
Secondary | Change in 10-Metre Walking Test (10MWT) | 10MWT is used to measure the time (and if required the number of steps) taken for subjects to cover a distance of ten meters from a standing start, when walking at their usual speed, as a measure of the change in aspects of their gait performance | At baseline (day 1-T1) and at the end (day 21 -T2) of the treatment. |
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