Smoking Cessation Via Text Messaging: Feasibility Testing of Stop My Smoking USA (SMS USA)
| Tracking Information | |||||
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| First Received Date ICMJE | March 15, 2011 | ||||
| Last Updated Date | January 24, 2012 | ||||
| Start Date ICMJE | June 2009 | ||||
| Primary Completion Date | December 2011 (final data collection date for primary outcome measure) | ||||
| Current Primary Outcome Measures ICMJE |
Continuous abstinence [ Time Frame: 3-months post-quit ] [ Designated as safety issue: No ] We will measure continuous abstinence as 5 or fewer cigarettes smoked since one's quit date: "Have you smoked at all, even just a puff, since [insert quit date]?" If yes, the respondent will be probed for how many cigarettes were smoked. Responses will be categorized into one of three options: A) No, not a puff; B) 1-5 cigarettes; C) More than 5 cigarettes. Abstinence will be defined by smoking five or fewer cigarettes. |
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| Original Primary Outcome Measures ICMJE | Same as current | ||||
| Change History | Complete list of historical versions of study NCT01516632 on ClinicalTrials.gov Archive Site | ||||
| Current Secondary Outcome Measures ICMJE |
Point prevalence [ Time Frame: Past 7 days ] [ Designated as safety issue: No ] A cigarette, even just a puff, within the last 7 days (yes/no) |
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| Original Secondary Outcome Measures ICMJE | Same as current | ||||
| Current Other Outcome Measures ICMJE | Not Provided | ||||
| Original Other Outcome Measures ICMJE | Not Provided | ||||
| Descriptive Information | |||||
| Brief Title ICMJE | Smoking Cessation Via Text Messaging: Feasibility Testing of Stop My Smoking USA | ||||
| Official Title ICMJE | Smoking Cessation Via Text Messaging: Feasibility Testing of SMS USA | ||||
| Brief Summary | The investigators are developing a testing a text messaging-based smoking cessation program called SMS (Stop My Smoking) USA. It will be tailored for the unique needs and smoking habits of young adults. The investigators hypothesize that those in the SMS USA intervention will be significantly more likely to be quit at 6-months compared to the attention-matched control group. |
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| Detailed Description | About one in four young adults are current smokers. Although over half report the desire to quit or cut down, quit rates in this age group have remained stagnant in the last ten years. Text messaging may represent a compelling intervention delivery method for smoking cessation for young adults because it is a medium they have widely adopted. Cell phone interventions also are unique because of their 'always on' capability - interventions are never far from the young adult's reach and they are received automatically instead of requiring the participant to initiate contact in order to receive the information. Dr. Ybarra, along with Drs. Holtrop and Graham, have developed SMS Turkey, an innovative behavioral intervention that uses text messaging to deliver CBT-based smoking cessation information to participants daily. Successful use of text messaging to deliver smoking cessation programs has been reported by Rodgers and colleagues in New Zealand and a replication study they are leading in the UK. These data provide optimism for the feasibility of text messaging-based smoking cessation programs in the United States. Using qualitative methods to inform design and content, and quantitative methods to assess the feasibility of the program, we propose to design and test SMS (Stop My Smoking) USA, a cell-phone based smoking cessation program for young adults ages 18-25. This innovative smoking cessation program uses technology widely adopted by young adults, an under-targeted population, to deliver a proactive, cognitive behavioral therapy (CBT)-based intervention. Our multidisciplinary team of researchers brings together expertise in Internet health and the design of tailored smoking cessation interventions. |
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| Study Type ICMJE | Interventional | ||||
| Study Phase | Phase 1 Phase 2 |
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| Study Design ICMJE | Allocation: Randomized Endpoint Classification: Efficacy Study Intervention Model: Parallel Assignment Masking: Single Blind (Subject) Primary Purpose: Treatment |
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| Condition ICMJE | Smoking Cessation | ||||
| Intervention ICMJE | Behavioral: SMS (Stop my Smoking) USA
Intervention participants receive text messages daily pre-and post-quit. Everyone receives messages 14 days prior to the Quit day, and through the day after Quit. Then, participants are 'pathed' to particular messages based upon their self-reported smoking status at Day 2 and Day 7 post quit, respectively. Those who are successful at quitting receive messages aimed at relapse prevention whereas those who have slipped receive messages aimed at getting the person to recommit to quitting and trying again. |
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| Study Arm (s) |
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| Publications * | Not Provided | ||||
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* Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline. |
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| Recruitment Information | |||||
| Recruitment Status ICMJE | Completed | ||||
| Enrollment ICMJE | 164 | ||||
| Completion Date | December 2011 | ||||
| Primary Completion Date | December 2011 (final data collection date for primary outcome measure) | ||||
| Eligibility Criteria ICMJE | Inclusion Criteria:
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| Gender | Both | ||||
| Ages | 18 Years to 25 Years | ||||
| Accepts Healthy Volunteers | Yes | ||||
| Contacts ICMJE | Contact information is only displayed when the study is recruiting subjects | ||||
| Location Countries ICMJE | United States | ||||
| Administrative Information | |||||
| NCT Number ICMJE | NCT01516632 | ||||
| Other Study ID Numbers ICMJE | R21CA135669, 5R21CA135669 | ||||
| Has Data Monitoring Committee | No | ||||
| Responsible Party | Center for Innovative Public Health Research | ||||
| Study Sponsor ICMJE | Center for Innovative Public Health Research | ||||
| Collaborators ICMJE |
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| Investigators ICMJE |
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| Information Provided By | Center for Innovative Public Health Research | ||||
| Verification Date | January 2012 | ||||
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ICMJE Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP |
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