Rehabilitation Exercise Using Digital Healthcare System in Patients With Anterior Cruciate Ligament Reconstruction
Study Details
Study Description
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.
| Condition or Disease | Intervention/Treatment | Phase |
|---|---|---|
|
N/A |
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.
Study Design
Arms and Interventions
| Arm | Intervention/Treatment |
|---|---|
| Experimental: Digital Healthcare System Rehabilitation
|
Device: Rehabilitation using Digital Healthcare System (Uincare Homeplus)
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.
Other Names:
|
| Active Comparator: Conventional Rehabilitation
|
Other: Conventional Rehabilitation
Home-based self-rehabilitation using brochure for 12 weeks post surgery.
|
Outcome Measures
Primary Outcome Measures
- 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
- 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.
- 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
- 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.
- 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.
- 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.
Eligibility Criteria
Criteria
Inclusion Criteria:
-
Patient who had anterior cruciate ligament reconstruction surgery
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Patient who is discharged to home after surgery
Exclusion Criteria:
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Patient who had previous history of anterior cruciate ligament reconstruction surgery in the past 6 months.
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Patient who had undergone bilateral anterior cruciate ligament reconstruction surgery.
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Patient who has knee joint disorders (rheumatoid arthritis, osteoarthritis) other than anterior cruciate ligament injury.
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Patient who has neurological deficit or infection in the affected knee joint.
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Patient who has severe comorbidity that inhibits exercise.
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Patient who cannot participate in post surgery rehabilitation
Contacts and Locations
Locations
| Site | City | State | Country | Postal Code | |
|---|---|---|---|---|---|
| 1 | Samsung Medical Center | Seoul | Gangnam-gu | Korea, Republic of | 06351 |
| 2 | Seoul National University Bundang Hospital | Seongnam-si | Gyeonggi-do | Korea, Republic of | 13620 |
Sponsors and Collaborators
- Seoul National University Bundang Hospital
- Ministry of Health, Republic of Korea
Investigators
None specified.Study Documents (Full-Text)
None provided.More Information
Publications
None provided.- B-2005/612-001(3)