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临床试验/NCT03902834
NCT03902834已完成不适用

Move for Surgery (MFS): Evaluating the Use of Wearable Technology for Preconditioning Before Thoracic Surgery

St. Joseph's Healthcare Hamilton2 个研究点 分布在 1 个国家目标入组 25 人开始时间: 2017年11月30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
25
试验地点
2
主要终点
The feasibility of Move for Surgery, as measured by a rate of compliance of >70% until program completion.

研究概览

简要总结

Wearable technology is increasingly being used to promote healthy behaviour. In this study, the investigators propose the development and evaluation of Move for Surgery, which utilizes a wearable activity bracelet (Fitbit) and proven behavioural change techniques, for preconditioning of patients prior to lung cancer surgery. The primary outcome of this study will be compliance with Move for Surgery, as a surrogate measure for feasibility. Secondary outcomes, including accrual rates, perioperative pulmonary complications, cost per patient, and patient satisfaction, will also be collected. The investigators have partnered with the Canadian Partnership Against Cancer (CPAC) and Lung Cancer Canada (LCC) to develop Move for Surgery. The ultimate goal of this preliminary study is to lay the groundwork for a subsequent comparative trial to evaluate the impact of Move for Surgery on postoperative complications in the thoracic surgery population.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Other
盲法
None

入排标准

性别
All
接受健康志愿者

入选标准

  • Eligible participants include patients with NSCLC set to undergo pulmonary resection.

排除标准

  • There will be no exclusion based on functional status in this feasibility study; rather, a subsequent analysis of participant demographics will be performed to inform future phases of this study.

结局指标

主要结局

The feasibility of Move for Surgery, as measured by a rate of compliance of >70% until program completion.

时间窗: 12 months

The feasibility of Move for Surgery, as measured by a rate of compliance of \>70% until program completion.

次要结局

  • Rate of accrual(12 months)
  • Cost per patient(12 months)
  • Patient-reported health-related quality of life(12 months)
  • Patient-reported health-related physical activity(12 months)
  • Perioperative patient complications(12 months)

研究者

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

Wael Hanna

Assistant Professor of Surgery

St. Joseph's Healthcare Hamilton

研究点 (2)

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