Assessing surgery risk through a walking test
Official title: FUNCTIONAL ASSESSMENT FOR SURGERY BY A TIMED WALK
Run by Unity Health Toronto · NCT06412367 · Data updated 2026-11-12
This study is testing if a six-minute walking test can help predict the risk of complications for patients over 40 who are having non-heart surgery.
Quick facts
| Study type | Observational |
|---|---|
| Ages | 40 Years and up |
| Sex | All |
| Enrollment | 1672 (estimated) |
| Sponsor | Unity Health Toronto Academic / other |
| Locations | 1 site (Toronto, Ontario) |
| Status | Recruiting |
| Started | June 10, 2024 |
| Main results expected | May 2028 |
| Study ends | September 2029 |
| Registry record updated | June 11, 2024 |
| Trial ID | NCT06412367 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Ideal candidates are individuals aged 40 and older with at least one risk factor for postoperative complications who are scheduled for elective non-cardiac surgery.
✕Probably not a fit
Patients undergoing endovascular or lower limb orthopedic surgeries, or those with contraindications to the 6MWT, may not benefit from this study.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
The FAST Walk study evaluates whether the six-minute walk test (6MWT) can predict the likelihood of complications in patients undergoing elective non-cardiac surgery. Participants aged 40 and older, who have at least one risk factor for postoperative complications, will complete the 6MWT prior to their surgery. The goal is to enhance patient care by identifying those at higher risk for complications based on their walking test results. This observational study is conducted at St. Michael's Hospital in Toronto.
Why it matters
Potential benefit: If successful, this study could lead to improved preoperative assessments and tailored care for patients undergoing major surgery.
How similar studies have gone: Similar studies using functional assessments like the 6MWT have shown promise in predicting surgical outcomes, suggesting this approach may be beneficial.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: 1. Age ≥40 years 2. ≥1 risk factors for postoperative complications 3. Elective non-cardiac surgery with expected post-surgery stay ≥2 days 4. Preoperative 6MWT is feasible 5. Working knowledge of official language(s) in country of study recruitment Exclusion Criteria: 1. Endovascular surgery 2. Lower limb orthopedic surgery 3. Contraindications to 6MWT
Where it's running
-
St. Michael's Hospital
Toronto, Ontario, Canada Recruiting
Study contacts
- Principal investigator: Duminda N Wijeysundera, MD PhD FRCPC — Unity Health Toronto
- Study coordinator: Duminda N Wijeysundera, MD PhD FRCPC
- Email: d.wijeysundera@utoronto.ca
- Phone: 416-864-5825
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How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.