Text Messaging for Smoking Cessation in College Health Clinics
- Conditions
- Cigarette Smoking
- Interventions
- Registration Number
- NCT02191033
- Lead Sponsor
- Yale University
- Brief Summary
This study is a randomized-controlled clinical trial which evaluates the efficacy of physician brief advice, nicotine replacement therapy and a 6-week course of text messaging in promoting cigarette smoking in smokers enrolled in college.
The primary hypothesis is that smokers receiving physician brief advice, nicotine replacement therapy, and text messaging will have higher quit rates that smokers receiving physician brief advice and nicotine replacement therapy alone.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 40
- Aged 18 through 24 years
- Enrolled as a full/part time college student
- A current smoker (Have smoked more than 100 cigarettes in their lifetime and now smoke every day or some days)
- English-speaking
- Interested in quitting
- Have a cell phone for personal use with an unlimited text messaging plan.
- History of hypersensitivity/allergy to nicotine patch;
- Serious arrhythmias - History of heart disease (myocardial infarction, severe chest pain, or coronary artery disease)
- Current pregnancy/breastfeeding/plan for pregnancy
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Arm && Interventions
Group Intervention Description Standard of care Smoking counseling Smoking counseling, nicotine patch Text messaging Smoking counseling Smoking counseling, nicotine patch, text messaging Text messaging Text messaging Smoking counseling, nicotine patch, text messaging Text messaging Nicotine patch Smoking counseling, nicotine patch, text messaging Standard of care Nicotine patch Smoking counseling, nicotine patch
- Primary Outcome Measures
Name Time Method Study Enrollment- Number of Participants Who Join the Study baseline We will report the number of persons who join the study.
Study Retention- Number of Participants Who Attend the 6- and 12-week Follow up Visits. 6- and 12- weeks We will determine the number of enrolled participants who follow up at the 6- and 12- week follow up visit.
- Secondary Outcome Measures
Name Time Method Smoking Abstinence 6- and 12- weeks biochemically confirmed point prevalence of self reported past 7-day abstinence
Trial Locations
- Locations (1)
Southern Connecticut State University
🇺🇸New Haven, Connecticut, United States