The Effect of Individualized Counseling, Phone Line Follow up, and Nicotine Chewing Gum on Smoking Cessatio
Phase 2
- Conditions
- smoking cessation.
- Registration Number
- IRCT201011025074N1
- Lead Sponsor
- Isfahan University of Medical Sciences, Vice Chancellor for Research
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- All
- Target Recruitment
- 112
Inclusion Criteria
Inclusion Criteria: Appeasing in preparation stage of smoking behavior; being in readiness to quit; age between 12-80 years old; not to be pregnant; and suffer from MI or CVA in last 3 weeks.
Exclusion criteria: There is no limitation for the participants exclusion.
Exclusion Criteria
Not provided
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Smoking cessation stability. Timepoint: baseline, 3 and 6 months after intervention. Method of measurement: Fagerstrom test, Diclemente and et al. Stages of change questionnaire.
- Secondary Outcome Measures
Name Time Method Relapse in smoking cessation. Timepoint: Baseline, 3 and 6 months after intervention. Method of measurement: Self reporting.
Related Research Topics
Explore scientific publications, clinical data analysis, treatment approaches, and expert-compiled information related to the mechanisms and outcomes of this trial. Click any topic for comprehensive research insights.
What molecular mechanisms underlie nicotine chewing gum's efficacy in smoking cessation?
How does individualized counseling compare to standard behavioral interventions for smoking cessation?
Which biomarkers predict response to nicotine replacement therapy in smokers?
What are the potential adverse events associated with nicotine chewing gum and how are they managed?
How effective is the combination of nicotine chewing gum and counseling compared to other pharmacotherapies like varenicline or bupropion?