N/A
Completed N=416
Clinical Trial of Smoking Cessation Mobile Phone Program
Source: ClinicalTrials.gov NCT02656745 ↗Enrolled (actual)
416
Serious AEs
0.0%
Results posted
Nov 2018
Primary outcomePrimary: Number of Participants Who Remain Active Users of the Program — 365 Participants
Summary
The Sponsor is doing a research study to assess the effects of a smartphone program designed to help users smoke less and eventually quit. When participants join, their involvement in the core study will last 8 weeks. After 8 weeks, they will have the option to continue using the program to guide their quit journey or participate in follow-up research.
Outcome Measures
| Outcome | Result | p-value |
|---|---|---|
| PRIMARY Number of Participants Who Remain Active Users of the Program |
365 | — |
| SECONDARY Number of Participants With Treatment-related Adverse Events |
19 | — |
| SECONDARY Efficacy - Smoking Cessation [7-day Abstinence & 30 Day Abstinence] |
188; 188; 109; 109 | — |
Eligibility Criteria
Inclusion Criteria
- Age 18 to 65
- Smokes at least 5 cigarettes daily
- Is interested in quitting in the next 30 days
- Owns an iPhone with iOS 8 or higher capabilities
- Willing and able to receive SMS text messages
- Able to comprehend the English-language and the informed consent form
- Lives in the United States
- Provides informed consent to participate in the study
- Able and willing to comply with study procedures as outlined in the protocol and informed consent form
Exclusion Criteria
- Unable or unwilling to provide informed consent
- Responds appropriately to any item in the Eligibility Questionnaire:
- Do you smoke at least 5 cigarettes a day? - must say YES
- Are you interested in quitting in the next 30 days? - must say YES
- Do you have access to an Apple iPhone with iOS 8 (or higher) capabilities and internet access? - must say YES
- Are you between 18-65 years old? - must say YES
- Do you currently live in the United States? - must say YES
- Are you currently using a mobile phone-based smoking cessation intervention? - must say NO
- Are you willing and able to receive SMS messages throughout the study? - must say YES
Data sourced from ClinicalTrials.gov (NCT02656745). 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.