Suppr超能文献

基于计算机视觉的膝关节骨关节炎患者运动管理系统的疗效:一项随机对照初步试验研究方案。

Efficacy of a computer vision-based system for exercise management in patients with knee osteoarthritis: a study protocol for a randomised controlled pilot trial.

机构信息

Sports Medicine Center, Sichuan University West China Hospital, Chengdu, Sichuan, China.

Department of Orthopedics and Orthopedic Research Institute, West China Hospital of Sichuan University, Chengdu, Sichuan, China.

出版信息

BMJ Open. 2024 Nov 5;14(11):e077455. doi: 10.1136/bmjopen-2023-077455.

Abstract

INTRODUCTION

This study aims to evaluate the efficacy of a computer vision system in guiding exercise management for patients with knee osteoarthritis (OA) by comparing functional improvement between a tele-rehabilitation versus an outpatient intervention program.

METHODS AND ANALYSIS

This is a prospective, single-blind, randomised controlled trial of 60 patients with knee OA who will be randomly assigned to exercise therapy (n=30) or control (n=30) . Both groups will receive treatment two times per week for 12 weeks. The primary outcome of the study will be assessed using the University of Western Ontario and McMaster University Osteoarthritis Index (WOMAC). The Knee Injury and Osteoarthritis Outcome Score will be assessed, as well as the visual analogue scale, quality of life score and physical fitness score. All observations will be collected at baseline and at weeks 4, 8 and 12 during the intervention period, as well as at weeks 4, 8, 12 and 24 during the follow-up visits after the end of the intervention.

ETHICS AND DISSEMINATION

This evaluator-blinded, prospective, randomised controlled study was approved by the Biomedical Ethics Review Committee of West China Hospital of Sichuan University.

TRIAL REGISTRATION NUMBER

ChiCTR2300070319.

摘要

简介

本研究旨在通过比较远程康复与门诊干预方案在膝关节骨关节炎(OA)患者运动管理中的疗效,评估计算机视觉系统在指导膝关节 OA 患者运动管理中的作用。

方法与分析

这是一项前瞻性、单盲、随机对照试验,纳入 60 例膝关节 OA 患者,将随机分为运动治疗组(n=30)和对照组(n=30)。两组患者均每周接受 2 次治疗,共 12 周。研究的主要结局指标采用西安大略和麦克马斯特大学骨关节炎指数(WOMAC)进行评估。还将评估膝关节损伤和骨关节炎结果评分(KOOS)、视觉模拟评分、生活质量评分和身体适应性评分。所有观察结果均在基线和干预期间的第 4、8 和 12 周,以及干预结束后的第 4、8、12 和 24 周的随访期间收集。

伦理与传播

本评估者盲法、前瞻性、随机对照研究已获得四川大学华西医院生物医学伦理审查委员会的批准。

注册号

ChiCTR2300070319。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f6f0/11552600/4b8dc6df35a1/bmjopen-14-11-g001.jpg

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验