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临床试验/NCT04541940
NCT04541940已完成不适用

TeleRehabilitation Following ACL Reconstruction

NYU Langone Health2 个研究点 分布在 1 个国家目标入组 16 人开始时间: 2020年10月1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
16
试验地点
2
主要终点
RTS (Return to Sport)

研究概览

简要总结

Telerehabilitation is a form of tele-treatment in which rehabilitation services are dispensed at patients' home utilizing video telecommunication services with real-time synchronous exchange of information. The advantages of telerehabilitation include reducing unnecessary travel to the hospital and person to person contact while maintaining social distancing. While some of the patients are truly staying at remote areas, others are unable to manage travel in the lockdown period. Telemedicine offers the opportunity to deliver rehabilitative services in the patients' home, closing geographic, physical, and motivational gaps. Punctuality on either side is also assured since the travel times are saved on both the ends.

The purpose of the proposed study is to evaluate telerehabilitation vs. in-person rehabilitation following ACL reconstruction. Objectives include assess return to sport and patient reported functional outcomes.

研究设计

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

入排标准

年龄范围
18 Years 至 40 Years(Adult)
性别
All
接受健康志愿者

入选标准

  • Scheduled for ACL reconstruction
  • Age 18-40
  • Ability to comply with a standardized postoperative protocol
  • Willing and able to provide consent

排除标准

  • Pregnant patient
  • Age >40 years, or < 18
  • Previous knee surgery
  • Unable to speak English or perform informed consent

结局指标

主要结局

RTS (Return to Sport)

时间窗: up to 1 year post-op

The day when the participant is able to fully participate in their sport, but not at their desired performance level.

次要结局

  • Visual Analogue Scale (VAS) Score(up to 1 year post-op)
  • International Knee Documentation Committee (IKDC) Score(up to 1 year post-op)
  • Knee Injury and Osteoarthritis Outcome Score (KOOS)(up to 1 year post-op)
  • ACL-RSI Questionnaire Score(up to 1 year post-op)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (2)

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