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Move For Surgery Preconditioning Program using a Wearable Activity Tracker (Fitbit) Intervention Group for Non-Small Cell Lung Cancer (MFS Trial)
Phase 3
Waitlist Available
Research Sponsored by St. Joseph's Healthcare Hamilton
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 24 months
Awards & highlights
MFS Trial Summary
This study is evaluating whether a preconditioning program can reduce the risk of complications after major chest surgery.
Eligible Conditions
- Non-Small Cell Lung Cancer
MFS Trial Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ 24 months
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~24 months
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Primary outcome measures
The of the comparative trial will be length of stay (LOS) in hospital after surgery, which will also be used to measure speed of recovery from surgery and postoperative complications.
Secondary outcome measures
will include differences in the 36-Item Short Form Health Survey (SF-36) scores before and after the intervention.
MFS Trial Design
2Treatment groups
Experimental Treatment
Active Control
Group I: Move For Surgery Preconditioning Program Intervention GroupExperimental Treatment1 Intervention
Group II: Standard Preoperative Care GroupActive Control1 Intervention
Treatment
First Studied
Drug Approval Stage
How many patients have taken this drug
Move For Surgery Preconditioning Program using a Wearable Activity Tracker (Fitbit) Intervention Group
2018
Completed Phase 3
~110
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Who is running the clinical trial?
Hamilton Academic Health Sciences OrganizationOTHER
20 Previous Clinical Trials
4,764 Total Patients Enrolled
St. Joseph's Healthcare HamiltonLead Sponsor
196 Previous Clinical Trials
25,442 Total Patients Enrolled
Frequently Asked Questions
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