Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
NA
300 participants
INTERVENTIONAL
2007-07-31
2011-06-30
Brief Summary
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Detailed Description
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Conditions
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Study Design
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RANDOMIZED
SINGLE_GROUP
PREVENTION
NONE
Study Groups
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1
Brief assistance with smoking abstinence
Standard brief advice
Brief general assistance with smoking cessation
2
Brief intervention to promote quitline utilization
Quitline intervention
Brief intervention designed specifically to encourage quitline utilization
Interventions
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Standard brief advice
Brief general assistance with smoking cessation
Quitline intervention
Brief intervention designed specifically to encourage quitline utilization
Eligibility Criteria
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Inclusion Criteria
* Current smoking before the scheduling of surgery, defined as \> 100 cigarettes lifetime consumption and self-reports of smoking either every day or some days. Patients who are in the midst of a quit attempt initiated since learning about surgery are eligible.
Exclusion Criteria
18 Years
ALL
No
Sponsors
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Mayo Clinic
OTHER
Responsible Party
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David Warner
MD
Principal Investigators
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David O. Warner, M.D.
Role: PRINCIPAL_INVESTIGATOR
Mayo Clinic
Locations
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Mayo Clinic
Rochester, Minnesota, United States
Countries
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References
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Warner DO, Klesges RC, Dale LC, Offord KP, Schroeder DR, Shi Y, Vickers KS, Danielson DR. Clinician-delivered intervention to facilitate tobacco quitline use by surgical patients. Anesthesiology. 2011 Apr;114(4):847-55. doi: 10.1097/ALN.0b013e31820d868d.
Other Identifiers
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06-004330
Identifier Type: -
Identifier Source: org_study_id
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