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Clinical Trials/NCT02724462
NCT02724462
Completed
N/A

Randomized Trial of An Innovative Smartphone Intervention for Smoking Cessation

Fred Hutchinson Cancer Center1 site in 1 country2,503 target enrollmentMay 27, 2017
ConditionsSmoking

Overview

Phase
N/A
Intervention
Not specified
Conditions
Smoking
Sponsor
Fred Hutchinson Cancer Center
Enrollment
2503
Locations
1
Primary Endpoint
30-day Point Prevalence Abstinence, Complete-case
Status
Completed
Last Updated
5 years ago

Overview

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.

Registry
clinicaltrials.gov
Start Date
May 27, 2017
End Date
December 27, 2019
Last Updated
5 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

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

Exclusion Criteria

  • The exclusion criteria are opposite of the inclusion criteria listed above.

Outcomes

Primary Outcomes

30-day Point Prevalence Abstinence, Complete-case

Time Frame: 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 Outcomes

  • 30-day Point Prevalence Abstinence, Missing=Smoking Imputation(12 months post randomization)

Study Sites (1)

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