Actively Recruiting
The STRIVE Before Surgery Trial
Led by Ottawa Hospital Research Institute · Updated on 2026-05-01
902
Participants Needed
1
Research Sites
377 weeks
Total Duration
On this page
Sponsors
O
Ottawa Hospital Research Institute
Lead Sponsor
C
Canadian Institutes of Health Research (CIHR)
Collaborating Sponsor
AI-Summary
What this Trial Is About
The STRIVE Before Surgery Trial evaluates patient-reported disability at 90 days after surgery following participating in a home-based multimodal prehabilitation program supported through an online platform. Half of the participants will be randomized into the prehabilitation group, while the other half will be randomized into the control group.
CONDITIONS
Official Title
The STRIVE Before Surgery Trial
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Age ≥18 years
- Scheduled, or on the pathway, for inpatient abdominal, thoracic, pelvic, head-and-neck or vascular surgery
- Expected surgery date between 3 and 12 weeks from enrollment
- Valid provincial health insurance number
- Access to internet-enabled device
- Email address
You will not qualify if you...
-
Inability to read and communicate in English
-
Cognitive impairment preventing ability to provide informed consent independently
-
No telephone/cell phone
-
Cardiac, neurological or orthopedic procedure
-
Surgery with no curative intent (palliative surgery)
-
Patient not interested in participating in the context of their TAPA score
-
Any of the following cardiovascular conditions:
- Severe valvular heart disease that limits a patient's ability to ambulate on level ground, or is associated with syncope or dyspnea
- Severe cardiac dysrhythmias that limit a patient's ability to ambulate on level ground, or is associated with syncope or dyspnea
- Recent myocardial infarction (within 6 weeks prior to enrollment - based on the Heart and Stroke Foundation's HeartWalk program)
AI-Screening
AI-Powered Screening
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Trial Site Locations
Total: 1 location
1
The Ottawa Hospital Research Institute
Ottawa, Ontario, Canada, K1H 8L6
Actively Recruiting
Research Team
E
Emily Hladkowicz, PhD
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
DOUBLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
2
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