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.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
OTHER
Masking
NONE
Enrollment
25
Use the wearable technology (Fitbit) and proven behavioural change techniques to precondition patients prior to lung cancer surgery
St. Joseph's Healthcare Hamilton
Hamilton, Ontario, Canada
The feasibility of Move for Surgery, as measured by a rate of compliance of >70% until program completion.
The feasibility of Move for Surgery, as measured by a rate of compliance of \>70% until program completion.
Time frame: 12 months
Rate of accrual
Rate of accrual
Time frame: 12 months
Perioperative patient complications
Perioperative patient complications
Time frame: 12 months
Cost per patient
Cost per patient
Time frame: 12 months
Patient-reported health-related quality of life
EuroQol-5Dimensions-5Levels (EQ-5D-5L)
Time frame: 12 months
Patient-reported health-related physical activity
International Physical Activity Questionnaire - Short Form (IPAQ-SF)
Time frame: 12 months
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