Skip to content

Early Virtual Reality Based Home Rehabilitation Program After Total Hip Arthroplasty

Functional Recovery Evaluation Following Total Hip Arthroplasty And Early Home Rehabilitation Program With A Virtual Reality Based Rehabilitation System

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04221425
Enrollment
44
Registered
2020-01-09
Start date
2019-03-01
Completion date
2021-02-16
Last updated
2021-11-08

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Osteoarthritis, Hip

Brief summary

Total hip replacement (THR) is one of the most common interventions in orthopedic surgery. Rehabilitation is essential for maximizing the effectiveness of the surgery. Tele-rehabilitation programs after orthopedic surgery have proven their effectiveness, validity and cost-efficacy. It seems of interest to test the potential advantages of early virtual reality based rehabilitation programs after total hip arthroplasty compared to standard care. The aim of the study is to evaluate the functional recovery following total hip arthroplasty and home telerehabilitation programs with a virtual reality based system.

Interventions

experimental group is equipped with a telerehabilitation system which comprises a tablet (VRRS tablet) and a set of inertial magnetic sensors. participants are invited to follow a daily rehabilitation exercise program provided via VRRS tablet

PROCEDUREstandard care

participants in the control group are invited to follow a daily rehabilitation exercise program and indications for the recovery as illustrated in the dimission booklets drawn up by the rehabilitation unit

Sponsors

I.R.C.C.S Ospedale Galeazzi-Sant'Ambrogio
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
50 Years to 70 Years
Healthy volunteers
No

Inclusion criteria

* males and females from 50 to 70 years old * patients undergoing total hip arthroplasty with Anterior Minimally Invasive Surgery (AMIS) * Body Mass Index ≤ 31 * Schooling: Lower secondary certificate * Home internet connection * Caregiver presence * Domiciled in the conurbation of Milan * Written informed consent and consent to all phases of the study

Exclusion criteria

* congenital or post traumatic morphological abnormalities * presence of neurological conditions or cancer * presence of implanted devices subjected to electromagnetic interference * epilepsy * informed refusal * Ongoing anticoagulant or immunosuppressive therapies before surgery * Self reported pregnancy

Design outcomes

Primary

MeasureTime frameDescription
Hip dysfunction and Osteoarthritis Outcome Score for Joint Replacement (HOOS JR)15 ± 1 days after the surgery (T3)the HOOS JR scale scores ranges from 0 to 100 where 0 represents total hip disability and 100 represents perfect hip health

Secondary

MeasureTime frameDescription
Hip dysfunction and Osteoarthritis Outcome Score for Joint Replacement (HOOS JR)baseline (before surgery (T0)), 4 ± 1 days after the surgery (T1), 7 ± 2 days after the surgery (T2)the HOOS JR scale scores ranges from 0 to 100 where 0 represents total hip disability and 100 represents perfect hip health
BARTHEL INDEX (BI)baseline (before surgery (T0)), 4 ± 1 days after the surgery (T1), 15 ± 1 days after the surgery (T3)the BI assesses the ability of an individual to care for him/herself. Its scores ranges from 0 to 100, where 100 represents complete independence
Functional Independence Measure (FIM)baseline (before surgery (T0)), 4 ± 1 days after the surgery (T1), 15 ± 1 days after the surgery (T3)The Functional Independence Measure (FIM) explores an individual's physical, psychological and social function. Its scores ranges from 18 (lowest) to 126 (highest)
Global Perceived Effect (GPE)15 ± 1 days after the surgery (T3)The GPE scale asks the patient to rate, on a numerical scale from 1 to 5, where lower scores correspond to worse perceived effect, how much has the treatment received helped

Countries

Italy

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026