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

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

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03902834
Enrollment
25
Registered
2019-04-04
Start date
2017-11-30
Completion date
2018-09-12
Last updated
2019-04-08

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Lung Cancer, Nonsmall Cell, Preconditioning

Brief summary

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.

Interventions

OTHERFitbit

Use the wearable technology (Fitbit) and proven behavioural change techniques to precondition patients prior to lung cancer surgery

Sponsors

St. Joseph's Healthcare Hamilton
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
OTHER
Masking
NONE

Eligibility

Sex/Gender
ALL
Healthy volunteers
No

Inclusion criteria

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

Exclusion criteria

* 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.

Design outcomes

Primary

MeasureTime frameDescription
The feasibility of Move for Surgery, as measured by a rate of compliance of >70% until program completion.12 monthsThe feasibility of Move for Surgery, as measured by a rate of compliance of \>70% until program completion.

Secondary

MeasureTime frameDescription
Rate of accrual12 monthsRate of accrual
Perioperative patient complications12 monthsPerioperative patient complications
Cost per patient12 monthsCost per patient
Patient-reported health-related quality of life12 monthsEuroQol-5Dimensions-5Levels (EQ-5D-5L)
Patient-reported health-related physical activity12 monthsInternational Physical Activity Questionnaire - Short Form (IPAQ-SF)

Countries

Canada

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026