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NCT05001100 Clinical Trial

A Rehabilitation With Virtual Reality in Patients After Hip Arthroplasty Surgery (VRRS2018)

Hip Disease Clinical Trial

— VRRS2018  

Official title:
A Rehabilitation With Virtual Reality in Patients After Hip Arthroplasty Surgery (VRRS2018)

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT05001100
Other study ID # VRRS2018
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date January 20, 2019
Est. completion date November 7, 2020

Study information
Verified date July 2021
Source Istituto Ortopedico Galeazzi
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

.Assessing efficacy of rehabilitation with virtual reality exercises compared to traditional rehabilitation in the patient's operated hip arthroplasty

Description:

Randomized controlled clinical study: Comparison of clinical efficacy between rehabilitation with virtual reality (VRRS) and traditional physiotherapy in post-surgical rehabilitation treatment in hospital. Motor clinical evaluations will be carried out in both groups. Vrrs Arm: 32 subjects will undergo a virtual motor-reality training during the post-surgical rehabilitation period. Physiotherapist's arm: 32 subjects with demographic characteristics similar to the subjects of the Vrrs arm will undergo the habitual rehabilitative physiotherapy. According to normal clinical practice, both groups perform a co-intervention in addition to the assigned group; Manual therapy with exercises and functional activity (walk and stairs).

Recruitment information / eligibility
Status Completed
Enrollment 64
Est. completion date November 7, 2020
Est. primary completion date October 10, 2020
Accepts healthy volunteers No
Gender All
Age group 45 Years to 80 Years
Eligibility Inclusion Criteria: - hip arthroplasty Exclusion Criteria: - patient with resence of neurological and psychiatric disorders - minor patient

Study Design

Related Conditions & MeSH terms

Intervention

Other:
• rehabilitation
rehabilitation

Locations
Country Name City State
Italy Irccs Istituto Ortopedico Galeazzi Milan

Sponsors (1)
Lead Sponsor Collaborator
Istituto Ortopedico Galeazzi

Country where clinical trial is conducted

Italy, 

Outcome
Type Measure Description Time frame Safety issue
Primary disability measurement WOMAC (Western Ontario and McMaster University) Osteoarthritis index on the 21st day
Secondary pain measurement visual analoge scale VAS on the 10st day
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