Rehabilitation Exercise Using Digital Healthcare System in Patients With Rotator Cuff Repair

Sponsor
Seoul National University Bundang Hospital (Other)
Overall Status
Recruiting
CT.gov ID
NCT04511377
Collaborator
Ministry of Health, Republic of Korea (Other)
115
1
2
32
3.6

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 rotator cuff repair surgery. 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. Simple Shoulder Test (SST), Pain (using Numerical rating scale), shoulder range of motion (ROM), Disability of Arm, Shoulder and Hand (DASH), Shoulder Pain and Disability Index (SPADI), quality of life using EQ-5D will be evaluation on enrollment, 6-weeks, 12-weeks and 24-weeks after enrollment.

Condition or Disease Intervention/Treatment Phase
  • Device: Rehabilitation using Digital Healthcare System (Uincare Homeplus)
  • Other: Conventional Rehabilitation
N/A

Detailed Description

Rotator cuff tear is one of the most common disorders affecting shoulder pain and disabilities of daily life. It is a disorder that can be caused by trauma, overuse, inappropriate usage of shoulder as well as degenerative change, which is increasing due to enlarged geriatric population. 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 aimed to compare the efficacy of the newly-developed digital healthcare system with conventional rehabilitation program.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
115 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Single (Outcomes Assessor)
Primary Purpose:
Treatment
Official Title:
New Model of Short-term Rehabilitation Exercise Training Using Digital Healthcare System in Patients With Rotator Cuff Repair; Randomized Controlled Study
Actual Study Start Date :
Jul 30, 2020
Anticipated Primary Completion Date :
Dec 31, 2022
Anticipated Study Completion Date :
Mar 31, 2023

Arms and Interventions

Arm Intervention/Treatment
Experimental: Digital Healthcare System Rehabilitation

Rehabilitation using Uincare Homeplus

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 rotator cuff repair post-op rehabilitation at home. Home-based self-rehabilitation using brochure for 6 weeks post surgery (same as the active comparator) Home-based self-rehabilitation using digital healthcare system(Uincare Homeplus) for 6 to 12 weeks post surgery.
Other Names:
  • Uincare Homeplus
  • Active Comparator: Conventional Rehabilitation

    Rehabilitation using Brochure

    Other: Conventional Rehabilitation
    Home-based self-rehabilitation using brochure for 12 weeks post surgery.

    Outcome Measures

    Primary Outcome Measures

    1. Change from baseline Simple Shoulder Test (SST) on the affected shoulder [Enrollment, 6-weeks, 12-weeks, 24-weeks]

      Simple Shoulder Test is a self-reported shoulder-specific questionnaire that measures functional limitations of the affected shoulder in patients with shoulder dysfunction. The SST consists of 12 questions with dichotomous (yes/ no) response options. score ranges from 0 to 100, higher score meaning better shoulder function.

    Secondary Outcome Measures

    1. Numerical Rating Scale (NRS) on the affected shoulder [Enrollment, 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 scores mean worse outcome.

    2. Range of Motion (ROM) on the affected shoulder [Enrollment, 6-weeks, 12-weeks, 24-weeks]

      Evaluation of change of ROM in the affected shoulder from baseline to 24 weeks

    3. Manual Muscle Test (MMT) on the affected arm [Enrollment, 6-weeks, 12-weeks, 24-weeks]

      Evaluation of change of MMT in the affected arm from baseline to 24 weeks Upper extremities MMT ranges from 0-25, higher scoring meaning better outcome.

    4. Disabilities of the Arm, Shoulder and Hand (DASH) on the affected arm [Enrollment, 6-weeks, 12-weeks, 24-weeks]

      The DASH is a 30-item self-report questionnaire designed to assess musculoskeletal disorders of the upper limb. The score ranges from 0 (no disability) to 100 (most severe disability) with higher score meaning worse outcome.

    5. Shoulder Pain and Disability Index (SPADI) on the affected shoulder [Enrollment, 6-weeks, 12-weeks, 24-weeks]

      The Shoulder Pain and Disability Index (SPADI) is a self-administered questionnaire that consists of two dimensions, one for pain and the other for functional activities. Overall total scores range from 0 to 130 with higher score indicating more shoulder dysfunction.

    6. Quality of Life using EQ-5D-5L [Enrollment, 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

    Ages Eligible for Study:
    50 Years and Older
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
    • Patient who had rotator cuff repair surgery

    • Patient who is discharged to home after surgery

    Exclusion Criteria:
    • Patient who has previous history of shoulder surgery on the affected shoulder

    • Patient who has severe neurological deficit or infection on the affected shoulder

    • Patient who has severe comorbidities (Ex: uncontrolled diabetes mellitus or rheumatoid arthritis) that inhibit affected shoulder rehabilitation

    • Patient who cannot participate rehabilitation program

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 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.
    Responsible Party:
    Jae-Young Lim, Professor, Seoul National University Bundang Hospital
    ClinicalTrials.gov Identifier:
    NCT04511377
    Other Study ID Numbers:
    • B-2005/612-001
    First Posted:
    Aug 13, 2020
    Last Update Posted:
    Jan 5, 2022
    Last Verified:
    Jan 1, 2022
    Individual Participant Data (IPD) Sharing Statement:
    Undecided
    Plan to Share IPD:
    Undecided
    Studies a U.S. FDA-regulated Drug Product:
    No
    Studies a U.S. FDA-regulated Device Product:
    No
    Keywords provided by Jae-Young Lim, Professor, Seoul National University Bundang Hospital
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Jan 5, 2022