Rehabilitation Exercise Using Digital Healthcare System in Patients With Anterior Cruciate Ligament Reconstruction
- Conditions
- Anterior Cruciate Ligament Injuries
- Interventions
- Other: Conventional RehabilitationDevice: Rehabilitation using Digital Healthcare System (Uincare Homeplus)
- Registration Number
- NCT04513327
- Lead Sponsor
- Seoul National University Bundang Hospital
- 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.
Recruitment & Eligibility
- Status
- UNKNOWN
- Sex
- All
- Target Recruitment
- 60
- Patient who had anterior cruciate ligament reconstruction surgery
- Patient who is discharged to home after surgery
- 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
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Arm && Interventions
Group Intervention Description Conventional Rehabilitation Conventional Rehabilitation - Digital Healthcare System Rehabilitation Rehabilitation using Digital Healthcare System (Uincare Homeplus) -
- Primary Outcome Measures
Name Time Method Changes from baseline Limb Symmetry Index (LSI) of lower extremities Enrollment, 2-weeks, 6-weeks, 12-weeks, 24-weeks LSI(%) = (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 Outcome Measures
Name Time Method Range of Motion (ROM) on the affected knee Enrollment, 2-weeks, 6-weeks, 12-weeks, 24-weeks Evaluation of change of ROM in the affected knee from baseline to 24 weeks
International Knee Documentation Committee (IKDC) score on the affected knee Enrollment, 2-weeks, 6-weeks, 12-weeks, 24-weeks IKDC 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.
Numerical Rating Scale (NRS) on the affected knee Enrollment, 2-weeks, 6-weeks, 12-weeks, 24-weeks Evaluation of pain of the affected shoulder using numerical rating scale (0-10, with score 0 indicating no pain). Higher score meaning worse pain.
Quality of Life using EQ-5D-5L Enrollment, 2-weeks, 6-weeks, 12-weeks, 24-weeks Evaluation 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.
Manual Muscle Test (MMT) on the affected lower extremities Enrollment, 2-weeks, 6-weeks, 12-weeks, 24-weeks Evaluation 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.
Trial Locations
- Locations (2)
Samsung Medical Center
🇰🇷Seoul, Gangnam-gu, Korea, Republic of
Seoul National University Bundang Hospital
🇰🇷Seongnam-si, Gyeonggi-do, Korea, Republic of