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临床试验/NCT02775188
NCT02775188撤回不适用

interACTION: A Portable Joint Function Monitoring and Training System to Supplement Home Exercise Programs Following Anterior Cruciate Ligament Reconstruction

University of Pittsburgh2 个研究点 分布在 1 个国家开始时间: 2016年7月最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
撤回
试验地点
2
主要终点
Value evaluated by the ratio of patient outcomes to costs of rehabilitation

研究概览

简要总结

The purpose of this study is to ascertain if home-based therapy with monitoring via telemedicine can overcome many barriers to compliance and improve rehabilitation following ACL reconstruction. Patients undergoing ACL Reconstruction will be followed for 6 weeks during their outpatient physical therapy treatment. Subjects will undergo weekly physical therapy or weekly physical therapy paired with InterACTION.

研究设计

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

入排标准

年龄范围
15 Years 至 30 Years(Child, Adult)
性别
All
接受健康志愿者

入选标准

  • Between 15 to 30 years of age;
  • Have undergone ACL Reconstruction;
  • Being referred for post-operative outpatient physical therapy;
  • Agree to and able to perform pre-designed exercises that they would normally perform in a physical therapy program after ACL Reconstruction.

排除标准

  • Patients undergoing concomitant meniscal repair or other surgical procedure requiring modification of post-operative physical therapy program;
  • Patients with BMI >40 at the time of surgery;
  • Individuals who are not free of any other co-disability or comorbidity that would specifically impede disallow or otherwise hinder performance of physical therapy exercises;

研究组 & 干预措施

Physical Therapy with InterACTION

Experimental

After ACL Reconstruction, subjects will undergo physical therapy 1 time per week supplemented by home exercise program with InterACTION device.

干预措施: interACTION (Device)

Physical Therapy

Other

After ACL Reconstruction, subjects will undergo physical therapy 1 time per week

干预措施: Standard of Care Physical Therapy (Other)

结局指标

主要结局

Value evaluated by the ratio of patient outcomes to costs of rehabilitation

时间窗: 6 weeks

Value will be evaluated by the ratio of patient outcomes to costs of rehabilitation

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

James J. Irrgang

PhD, PT

University of Pittsburgh

研究点 (2)

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