Smoking Clinical Trial
Official title:
Randomized Trial of An Innovative Smartphone Intervention for Smoking Cessation
Verified date | November 2020 |
Source | Fred Hutchinson Cancer Research Center |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
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.
Status | Completed |
Enrollment | 2503 |
Est. completion date | December 27, 2019 |
Est. primary completion date | December 27, 2019 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | All |
Age group | 18 Years and older |
Eligibility | Inclusion Criteria: - 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. Exclusion Criteria: - The exclusion criteria are opposite of the inclusion criteria listed above. |
Country | Name | City | State |
---|---|---|---|
United States | Fred Hutchinson Cancer Research Center | Seattle | Washington |
Lead Sponsor | Collaborator |
---|---|
Fred Hutchinson Cancer Research Center | National Cancer Institute (NCI), University of Washington |
United States,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | 30-day Point Prevalence Abstinence, Complete-case | 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. | 12 months post randomization | |
Secondary | 30-day Point Prevalence Abstinence, Missing=Smoking Imputation | 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. | 12 months post randomization |
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