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

S

St. Joseph's Healthcare Hamilton

Status

Completed

Conditions

Lung Cancer, Nonsmall Cell
Preconditioning

Treatments

Other: Fitbit

Study type

Interventional

Funder types

Other

Identifiers

NCT03902834
BFCRS-333417

Details and patient eligibility

About

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.

Enrollment

25 patients

Sex

All

Volunteers

No Healthy Volunteers

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.

Trial design

Primary purpose

Other

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

25 participants in 1 patient group

Intervention
Experimental group
Treatment:
Other: Fitbit

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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