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N/A Completed N=319 Other

Outcomes From a Mobile Smoking Cessation Program During a Monitoring Period of 6 Months

Source: ClinicalTrials.gov NCT03295643 ↗
Enrolled (actual)
319
Serious AEs
0.0%
Results posted
Nov 2022
Primary outcomePrimary: Number of Participants Who Completed the Explore Stage — 283 Participants

Summary

Prospective, open label, single center clinical study enrolling 260 subjects in a mobile smoking cessation program using a smartphone app and a handheld breath sensor with coaching support over a six month period.

Outcome Measures

OutcomeResultp-value
PRIMARY
Number of Participants Who Completed the Explore Stage
283
PRIMARY
Number of Participants Who Completed the Build Stage
183
PRIMARY
Number of Participants Who Completed the Mobilize Stage
139
PRIMARY
Number of Participants Who Completed the Quit Stage
131
PRIMARY
Number of Participants Who Completed the Secure Stage
126
SECONDARY
Readiness to Quit and Goals Related to Smoking Behavior
94; 176; 11; 157; 114; 10
SECONDARY
Average Percentage Change in Cigarettes Per Day (CPD) by the Pre-Quit Stage
-44.5
SECONDARY
Weeks of Active Engagement
12.4
SECONDARY
Number of Participants Who Completed the Program
272
SECONDARY
Quit Attempts
2.4
SECONDARY
Quit Rate 7-day Point Prevalence
102
SECONDARY
Quit Rate 30-day Point Prevalence
88
SECONDARY
Number of Participants Who Reported Pivot Increased Their Motivation to Stop Smoking
233
SECONDARY
Confidence to Quit
4.2; 5.9; 6.4; 7.4
SECONDARY
Difficulty Maintaining Quit
3.1; 4.9; 5.7; 6.8

Eligibility Criteria

Inclusion Criteria

  • 18-65 years of age
  • English speaking
  • Smokes daily
  • Smokes 5 or more cigarettes per day
  • Owns and uses a smartphone (iPhone 5 and above, operating system iOS 9.0 and above, or, Android 4.4 and above, operating system Android 4.4 and above)
  • Employed at least 20 hours per week
  • Lives in the USA
  • Understands and willing to sign the Informed Consent Form
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT03295643). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication. Informational only — not medical advice.

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