ROSCAP: Reduction of Smoking in Cardiac Patients Study

This study has been completed.
Sponsor:
Information provided by:
Minneapolis Veterans Affairs Medical Center
ClinicalTrials.gov Identifier:
NCT00301626
First received: March 10, 2006
Last updated: October 23, 2008
Last verified: April 2005

March 10, 2006
October 23, 2008
October 2000
Not Provided
Smoking reduction
Same as current
Complete list of historical versions of study NCT00301626 on ClinicalTrials.gov Archive Site
Smoking cessation, biomarker measures
Same as current
Not Provided
Not Provided
 
ROSCAP: Reduction of Smoking in Cardiac Patients Study
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Background. The ROSCAP Study was a randomized controlled trial in heart disease patients to test the effect of a smoking reduction intervention on cigarettes per day (cpd) and biochemical and clinical indicators of tobacco exposure. .

Not Provided
Interventional
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Allocation: Randomized
Endpoint Classification: Efficacy Study
Intervention Model: Parallel Assignment
Masking: Open Label
  • Nicotine Dependence
  • Tobacco Dependence
  • Cardiac Disease
Behavioral: smoking reduction intervention (including NRT)
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*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Completed
180
January 2005
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Inclusion Criteria:

  • smoked at least 15 cigarettes per day and had one of 11 cardiovascular disorders: history of myocardial infarction, coronary artery bypass surgery, angioplasty, stent placement, thrombolytic therapy, angina, arrhythmia, a history of cardiac arrest, greater than 50% coronary artery stenosis by angiography, ischemia on exercise tolerance testing or congestive heart failure, required to confirm that they were unwilling or uninterested in setting a stop smoking date in the next 30 days.

Exclusion Criteria:

  • 1) unstable angina within the past 2 weeks, 2) unstable psychiatric or substance use disorders or 3) contraindications to nicotine replacement therapy (including pregnancy or intention to become pregnant)
Both
18 Years to 80 Years
No
Contact information is only displayed when the study is recruiting subjects
United States
 
NCT00301626
DA13333-02
Not Provided
Not Provided
National Institutes of Health (NIH)
Not Provided
Principal Investigator: Anne Joseph, MD, MPH Minneapolis VAMC & University of Minnesota
Minneapolis Veterans Affairs Medical Center
April 2005

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP