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临床试验/NCT04629417
NCT04629417已完成不适用

Measuring Adherence to Home Shoulder Physiotherapy With Artificial Intelligence

Sunnybrook Health Sciences Centre2 个研究点 分布在 1 个国家目标入组 103 人开始时间: 2019年5月14日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
103
试验地点
2
主要终点
Physiotherapy participation (smart watch inertial data)

研究概览

简要总结

An important part of recovery for shoulder injuries, is sticking to the exercise regimen that is prescribed by a physiotherapist. Currently, there is no proper way to measure whether patients are correcting doing their prescribed exercises at home. Researchers at Sunnybrook have tested out a Smart Physiotherapy Recognition System (SPARS), which consists of a watch that patients can wear while they are performing their physiotherapy exercises. The watch aims to learn how the exercises are done correctly when worn during supervised physiotherapy sessions, and then to record and compare whether those same exercises are being done correctly in a home setting. The main objectives of this study aims to test whether the SPARS system can effectively measure whether physiotherapy exercises are being done properly when they are done without physiotherapist supervision. Secondly, to examine whether the recovery process after shoulder injuries is improved if patients perform the physiotherapy exercises correctly.

详细描述

A research assistant will conduct in-person data collection on 120 patients, by recording patients' exercises during their supervised physiotherapy sessions each week using the SPARS smart watch. Each patient will wear smart watch on their affected arm only when performing prescribed exercises, and the watch will start recording inertial sensor data once the patient puts the watch on. The injured worker population will be recruited from referrals made to the Sunnybrook Working Condition Program (WCP) at the Holland Centre for a work-related shoulder injury. The patient population that is being funded by OHIP, will be recruited from referrals Sunnybrook Shoulder and Upper Extremity Program. Data collection will be collected at baseline (at time of informed consent), and at each supervised physiotherapy session during the course of a patient's treatment. A research assistant will be required to attend a minimum of one supervised physiotherapy session for each patient every two weeks, and record exercise type and technique, alongside the inertial data collection, based on feedback from the treating physiotherapist. Follow-up outcomes such as surveys and shoulder testing will be done at 6 weeks, monthly at a maximum of 3 months (OHIP-patients) and 5 months (WSIB) patients, final treatment session (if different than maximum amount), and 1 year after.

研究设计

研究类型
Interventional
分配方式
Non Randomized
干预模型
Parallel
主要目的
Treatment
盲法
None

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Males and females over the age of 18
  • Be diagnosed with rotator cuff tendinosis, shoulder impingement syndrome or a rotator cuff tear
  • Will be undergoing planned conservative management
  • Be able to participate in home physiotherapy exercises

排除标准

  • Upper extremity neurological deficit
  • Have had a previous failed surgery on the shoulder that is currently being treated
  • Undergoing simultaneous treatment for both shoulders

结局指标

主要结局

Physiotherapy participation (smart watch inertial data)

时间窗: Up to 3-5 months

Watch will begin recording inertial sensor data when it is put on during supervised and home physiotherapy exercises, and will stop recording when it is removed.

次要结局

  • Work status(Up to 1 year)
  • Numeric Pain Rating Scale (NPRS)(Up to 1 year)
  • The Disabilities of the Arm, Shoulder and Hand (DASH) Score(Up to 1 year)
  • Strength testing(Up to 12 weeks)
  • Shoulder active range of motion(Up to 12 weeks)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (2)

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