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Rehabilitation Exercise Using Digital Healthcare System in Patients With Anterior Cruciate Ligament Reconstruction

New Model of Short-term Rehabilitation Exercise Training Using Digital Healthcare System in Patients With Anterior Cruciate Ligament Reconstruction; Randomized Controlled Study

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04513327
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

Anterior Cruciate Ligament Injuries

Keywords

Anterior Cruciate Ligament Reconstruction, 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 anterior cruciate ligament reconstruction. 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. Limb Symmetry Index (LSI), Pain (using Numerical rating scale), knee joint range of motion (ROM), lower extremities motor power (using Manual muscle test), International Knee Documentation Committee (IKDC) and quality of life using EQ-5D-5L will be evaluation on enrollment, 2-weeks, 6-weeks, 12-weeks and 24-weeks after enrollment.

Detailed description

Anterior cruciate ligament(ACL) is a vital structure in the knee maintaining the stability and due to increased population engaging in sports activities, the ACL injury is becoming more prevalent among young adults. Rehabilitation after ACL reconstruction is essential to restore knee function and many factors including age, degree of sports activities engagement, weight bearing should be considered when organizing rehabilitation programs. Knee joint stiffness and weakness of knee flexor/extensor muscles are common problems following the surgery which are related to improper rehabilitation after ACL reconstructions. 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 newlydeveloped 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 anterior cruciate ligament reconstruction post-op rehabilitation at home. Home-based self-rehabilitation using brochure for 2 weeks post surgery (same as the active comparator) Home-based self-rehabilitation using digital healthcare system(Uincare Homeplus) for 2 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
20 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Patient who had anterior cruciate ligament reconstruction surgery * Patient who is discharged to home after surgery

Exclusion criteria

* Patient who had previous history of anterior cruciate ligament reconstruction surgery in the past 6 months. * Patient who had undergone bilateral anterior cruciate ligament reconstruction surgery. * Patient who has knee joint disorders (rheumatoid arthritis, osteoarthritis) other than anterior cruciate ligament injury. * Patient who has neurological deficit or infection in the affected knee joint. * Patient who has severe comorbidity that inhibits exercise. * Patient who cannot participate in post surgery rehabilitation

Design outcomes

Primary

MeasureTime frameDescription
Changes from baseline Limb Symmetry Index (LSI) of lower extremitiesEnrollment, 2-weeks, 6-weeks, 12-weeks, 24-weeksLSI(%) = (involved limb knee flexor and extensor manual muscle test score / uninvolved limb knee flexor and extensor manual muscle test score \* 100). LSI ranges from 0-100 with higher score meaning better limb symmetry.

Secondary

MeasureTime frameDescription
Numerical Rating Scale (NRS) on the affected kneeEnrollment, 2-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). Higher score meaning worse pain.
Range of Motion (ROM) on the affected kneeEnrollment, 2-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, 2-weeks, 6-weeks, 12-weeks, 24-weeksEvaluation of change of MMT in the affected lower extremities from baseline to 24 weeks. Affected lower extremity MMT ranges from 0-25 with higher score meaning better motor power.
International Knee Documentation Committee (IKDC) score on the affected kneeEnrollment, 2-weeks, 6-weeks, 12-weeks, 24-weeksIKDC score is a self-reported measure, 18 items (7 on symptoms, 1 on participation in sports, 9 on daily activities, and 1 on current knee function). IKDC score ranges from 0-100, with higher score meaning better function.
Quality of Life using EQ-5D-5LEnrollment, 2-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.

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 5, 2026