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Rehabilitation Exercise Using Digital Healthcare System in Patients With Total Knee Arthroplasty

New Model of Short-term Rehabilitation Exercise Training Using Digital Healthcare System in Patients With Total Knee Arthroplasty; Randomized Controlled Study

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04513353
Enrollment
60
Registered
2020-08-14
Start date
2020-07-30
Completion date
2023-03-31
Last updated
2022-01-05

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

Conditions

Osteo Arthritis Knee

Keywords

Total Knee Arthroplasty, Post-Operative Rehabilitation, Digital Healthcare System

Brief summary

The study aims to examine the effect of short-term rehabilitation exercise support using digital healthcare system (Uincare homeplus) in the patients with total knee arthroplasty. The study is a two-arm prospective randomized controlled study comparing the effect of rehabilitation exercise digital healthcare system at home with conventional brochure-based home exercise. Gait speed (4-meter), Pain (using Numerical rating scale), knee joint range of motion (ROM), lower extremities motor power (using Manual muscle test), Western Ontario and McMaster Universities Osteoarthritis Index (WOMAC), Berg Balance Scale (BBS) and quality of life using EQ-5D-5L will be evaluation on enrollment, 3-weeks, 6-weeks, 12-weeks and 24-weeks after enrollment.

Detailed description

Total knee arthroplasty is treatment of choice for knee degenerative arthritis patients who are unresponsive to non-operative management including medications and physical therapies. Total knee arthroplasty is an effective treatment enhancing the joint range of motion as well as reducing pain and correcting deformities which leads to better patient function with better quality of life. Current method of post-operative rehabilitation is home-based self rehabilitation using brochure, combined with one or two times of education at the hospital before discharge. Patients often find difficulty in doing rehabilitation by themselves at home without supervision which resulted in decreased compliance. With development of technologies using multi-motion sensor and AR(augmented-reality) system, the investigators have developed a digital healthcare system(Uincare Homeplus) which can supplement patients' rehabilitation at home by giving them proper instructions as well as feedback. In this prospective randomized controlled study, the investigators aim to compare the efficacy of the newly-developed digital healthcare system with conventional rehabilitation program.

Interventions

Uincare Homeplus is a device using infrared, kinect camera and motion capture technology to track 3D motion of the patients' posture and joint articulations. It also has embedded exercise training software dedicated to total knee arthroplasty post-op rehabilitation at home. Home-based self-rehabilitation using brochure for 3 weeks post surgery (same as the active comparator) Home-based self-rehabilitation using digital healthcare system(Uincare Homeplus) for 3 to 12 weeks post surgery.

OTHERConventional Rehabilitation

Home-based self-rehabilitation using brochure for 12 weeks post surgery.

Sponsors

Ministry of Health, Republic of Korea
CollaboratorOTHER_GOV
Seoul National University Bundang Hospital
Lead SponsorOTHER

Study design

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

Eligibility

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

Inclusion criteria

* Patient who had total knee arthroplasty * Patient who is discharged to home after surgery

Exclusion criteria

* Patient who had previous history of high tibial osteotomy on the affected lower extremities. * Patient who had history of lower extremities joint revision arthroplasty in the past 6 months. * Patient who has severe comorbidity that inhibits exercise. * Patient who has major neurological deficits on the lower extremities. * Patient who cannot participate in post surgery rehabilitation

Design outcomes

Primary

MeasureTime frameDescription
Changes from Baseline Gait SpeedEnrollment, 3-weeks, 6-weeks, 12-weeks, 24-weeksGait Speed is measured by the time required to walk 4-meters in plain indoor. Shorter time required to complete 4-meter walk means better gait function.

Secondary

MeasureTime frameDescription
Range of Motion (ROM) on the affected kneeEnrollment, 3-weeks, 6-weeks, 12-weeks, 24-weeksEvaluation of change of ROM in the affected knee from baseline to 24 weeks
Manual Muscle Test (MMT) on the affected lower extremitiesEnrollment, 3-weeks, 6-weeks, 12-weeks, 24-weeksEvaluation of change of MMT in the affected lower extremities from baseline to 24 weeks. affected lower extremities MMT scales from 0-25, higher score meaning better outcome.
Numerical Rating Scale (NRS) on the affected kneeEnrollment, 3-weeks, 6-weeks, 12-weeks, 24-weeksEvaluation of pain of the affected shoulder using numerical rating scale (0-10, with score 0 indicating no pain). the higher score means worse pain.
Berg Balance Scale (BBS)Enrollment, 3-weeks, 6-weeks, 12-weeks, 24-weeksBBS is a 14-item objective measure that assess static balance and fall risk in adults. BBS score ranges from 0-56, with higher score meaning better balance.
Quality of Life using EQ-5D-5LEnrollment, 3-weeks, 6-weeks, 12-weeks, 24-weeksEvaluation of quality of life using EQ-5D-5L. This scale is numbered from -0.066 to 0.904. Lower value means worse quality of life
Western Ontario and McMaster Universities Osteoarthritis Index (WOMAC) on the affected kneeEnrollment, 3-weeks, 6-weeks, 12-weeks, 24-weeksThe WOMAC is a self-administered questionnaire used in the evaluation of knee osteoarthritis. It is consisted with 24 items divided into 3 subscales; Pain, Stiffness and Physical function. WOMAC score ranges from 0-96 with higher score meaning worse pain, stiffness and function.

Countries

South Korea

Contacts

Primary ContactJay-Young Lim, M.D., Ph. D
drlim1@snu.ac.kr+82-31-787-7732

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 11, 2026