Peri Operative Smoking Cessation Program
Development and Implementation of a Peri Operative Smoking Cessation Program With Computer Based Patient Education.
1 other identifier
interventional
345
1 country
3
Brief Summary
Implementation of a perioperative smoking cessation program with computer based patient education increases the rate of short term (1 month) and long term (6 month) reduces the incidence of perioperative complications in elective surgical patients.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for not_applicable
Started Jul 2013
Typical duration for not_applicable
3 active sites
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
July 1, 2013
CompletedFirst Submitted
Initial submission to the registry
January 31, 2014
CompletedFirst Posted
Study publicly available on registry
February 3, 2014
CompletedPrimary Completion
Last participant's last visit for primary outcome
June 1, 2015
CompletedStudy Completion
Last participant's last visit for all outcomes
June 1, 2015
CompletedDecember 4, 2015
December 1, 2015
1.9 years
January 31, 2014
December 3, 2015
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Quit rate
we will do urine cotinine analysis to confirm the abstinence
6 month
Secondary Outcomes (1)
Surgical outcome
1 month
Study Arms (1)
computer based patient education
EXPERIMENTALThe patients will complete a pre module and post module set of questions to determine whether their knowledge about peri operative smoking cessation increase smoking has changed. According to their willingness and eligibility, pharmacotherapy will be given.
Interventions
Eligibility Criteria
You may qualify if:
- Patients\> 18 years of age
- self reported smokers ( daily or non daily smokers)
- Scheduled for elective surgical procedures
You may not qualify if:
- patients who cannot read and understand English
- Have any form of cognitive impairment
- Do not have a telephone
- Drug or alcohol abuser dependence within the past year
- Patients whop are already on pharmacotherapy for smoking cessation.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (3)
Mount Sinai Hospital
Toronto, Ontario, M5G 1X5, Canada
Toronto Western Hospital
Toronto, Ontario, Canada
Womens College Hospital
Toronto, Ontario, Canada
Related Publications (1)
Wong J, Raveendran R, Chuang J, Friedman Z, Singh M, Patras J, Wong DT, Chung F. Utilizing Patient E-learning in an Intervention Study on Preoperative Smoking Cessation. Anesth Analg. 2018 May;126(5):1646-1653. doi: 10.1213/ANE.0000000000002885.
PMID: 29517567DERIVED
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Jean Wong, FRCPC
Associate professor, dewpartment of anesthesia. Toronto Western Hospital, University Health Network, University of Toronto, Toronto, Ontario
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- NA
- Masking
- NONE
- Purpose
- PREVENTION
- Intervention Model
- SINGLE GROUP
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
January 31, 2014
First Posted
February 3, 2014
Study Start
July 1, 2013
Primary Completion
June 1, 2015
Study Completion
June 1, 2015
Last Updated
December 4, 2015
Record last verified: 2015-12