Trial of An Innovative Smartphone Intervention for Smoking Cessation
- Conditions
- Smoking
- Interventions
- Behavioral: Smartphone-delivered Intervention (SmartQuit)
- Registration Number
- NCT02724462
- Lead Sponsor
- Fred Hutchinson Cancer Center
- Brief Summary
The goal of this study is to determine whether the novel smartphone app (SmartQuit) provides higher quit rates than the current standard smoking cessation app.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 2503
- age 18 or older
- smokes at least five cigarettes daily for at least past 12 months
- wants to quit cigarette smoking in the next 30 days
- if concurrently using any other nicotine or tobacco products, wants to quit using them within the next 30 days
- interested in learning skills to quit smoking
- willing to be randomly assigned to either condition
- resides in US
- has at least daily access to their own personal Apple iPhone, Android, or Windows Phone
- knows how to login and download a smartphone application
- willing and able to read in English
- not using other smoking cessation interventions (including apps or our other intervention studies).
- willing to complete all three follow-up surveys
- provide email, phone, and mailing address.
- The exclusion criteria are opposite of the inclusion criteria listed above.
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Arm && Interventions
Group Intervention Description Experimental Smartphone-delivered Intervention (SmartQuit) This is the experimental arm of the study. This includes receiving the novel/experimental smartphone smoking cessation app. Therapy description withheld to protect the integrity of the study.
- Primary Outcome Measures
Name Time Method 30-day Point Prevalence Abstinence, Complete-case 12 months post randomization Percentage of participants reporting no smoking in the past 30 days, 12 months post-treatment. Participants missing follow-up data are excluded for the complete-case analysis. Exact 2-sided CI was based on the observed proportion of participants.
- Secondary Outcome Measures
Name Time Method 30-day Point Prevalence Abstinence, Missing=Smoking Imputation 12 months post randomization Percentage of participants reporting no smoking in the past 30 days, 12 months post-treatment. Participants missing follow-up data are imputed as still smoking. Exact 2-sided CI was based on the observed proportion of participants.
Trial Locations
- Locations (1)
Fred Hutchinson Cancer Research Center
🇺🇸Seattle, Washington, United States