← Back to Search

Behavioral Intervention for Preoperative Care in Surgery (Pre-Op Trial)

N/A
Recruiting
Led By Kyle Kirkham, MD
Research Sponsored by Ottawa Hospital Research Institute
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 6 months
Awards & highlights

Pre-Op Trial Summary

This trial evaluates the effect of a behavioral intervention on reducing low-value pre-op tests in low risk surgeries. It will be conducted in 22 hospitals in Ontario, Canada.

Who is the study for?
This trial is for hospitals in Ontario, Canada that frequently order routine preoperative tests and patients aged 18 or older undergoing low-risk surgeries like endoscopy, eye surgery, knee arthroscopy, or hernia repair. Hospitals with emergency elective chest X-rays and/or electrocardiograms are excluded.Check my eligibility
What is being tested?
The study is testing a behavioral intervention aimed at anesthesiologists and surgeons to see if it reduces unnecessary preoperative tests (like ECGs and chest X-rays) in patients having low-risk surgeries. It's being conducted across 22 hospitals.See study design
What are the potential side effects?
Since this trial focuses on reducing test orders rather than administering drugs or medical procedures, there aren't direct side effects as you would expect from medication trials.

Pre-Op Trial Timeline

Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~6 months
This trial's timeline: 3 weeks for screening, Varies for treatment, and 6 months for reporting.

Treatment Details

Study Objectives

Outcome measures can provide a clearer picture of what you can expect from a treatment.
Primary outcome measures
Pre-operative testing
Secondary outcome measures
All-cause mortality
Economic Evaluation
Fidelity evaluation
+4 more

Pre-Op Trial Design

2Treatment groups
Experimental Treatment
Active Control
Group I: De-implementationExperimental Treatment1 Intervention
A multi-behaviour technique will be used along with theoretical domains framework. Clinicians will be provided with continuing multi-behaviour component intervention to increase accountability for preoperative test ordering in patients having low risk surgeries.
Group II: ComparatorActive Control1 Intervention
Standard of care

Find a Location

Who is running the clinical trial?

Ottawa Hospital Research InstituteLead Sponsor
561 Previous Clinical Trials
2,785,472 Total Patients Enrolled
Canadian Institutes of Health Research (CIHR)OTHER_GOV
1,345 Previous Clinical Trials
26,453,492 Total Patients Enrolled
Kyle Kirkham, MDPrincipal InvestigatorDepartment of Anaesthesia, Toronto Western Hospital, University of Toronto

Frequently Asked Questions

These questions and answers are submitted by anonymous patients, and have not been verified by our internal team.

Is the enrollment period for this research project currently open?

"Clinicaltrials.gov informs us that this study is actively enrolling volunteers, with the first records showing up on January 1st 2024 and most recently modified on October 31st 2023."

Answered by AI

What is the cohort size of participants in this experiment?

"Affirmative, clinicaltrials.gov's records reflect that this experiment is actively seeking participants. The first publication of the study was made on January 1st 2024 and it has since been updated on October 31st 2023. This trial requires 22 test subjects to be recruited from 4 distinct sites."

Answered by AI

How many medical facilities are currently executing this research protocol?

"Presently, 4 different sites are running this clinical trial. Participants in the Kitchener, London and Stratford areas have convenient access to these locations as well as an additional 4 other nearby cities. To facilitate participation and minimize travel demands, it is advisable to select a clinic closest to you."

Answered by AI
~15 spots leftby Jan 2025