Smoking Cessation Via Text Messaging: Feasibility Testing of Stop My Smoking USA (SMS USA)

This study has been completed.
Sponsor:
Collaborators:
Michigan State University
The University of Texas Health Science Center, Houston
Information provided by (Responsible Party):
Center for Innovative Public Health Research
ClinicalTrials.gov Identifier:
NCT01516632
First received: March 15, 2011
Last updated: January 24, 2012
Last verified: January 2012

March 15, 2011
January 24, 2012
June 2009
December 2011   (final data collection date for primary outcome measure)
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.
Same as current
Complete list of historical versions of study NCT01516632 on ClinicalTrials.gov Archive Site
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)
Same as current
Not Provided
Not Provided
 
Smoking Cessation Via Text Messaging: Feasibility Testing of Stop My Smoking USA
Smoking Cessation Via Text Messaging: Feasibility Testing of SMS USA

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.

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.

Interventional
Phase 1
Phase 2
Allocation: Randomized
Endpoint Classification: Efficacy Study
Intervention Model: Parallel Assignment
Masking: Single Blind (Subject)
Primary Purpose: Treatment
Smoking Cessation
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.
  • Experimental: Smoking cesssation via text messaging
    The 6-week smoking cessation program
    Intervention: Behavioral: SMS (Stop my Smoking) USA
  • Active Comparator: Attention matched control
    Messages aimed at improving one's sleep and increasing one's fitness, along with general messages about the most well known health dangers of smoking. Messages sent on the same schedule as the intervention group.
    Intervention: Behavioral: SMS (Stop my Smoking) USA
Not Provided

*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Completed
164
December 2011
December 2011   (final data collection date for primary outcome measure)

Inclusion Criteria:

  • 28 cigarettes or more per week (at least 4/day) and on at least 6 days/week.
  • Owning a text-capable cell phone and cognizant of how to send and receive text messages
  • Currently enrolled or intending to enroll in an unlimited text messaging plan
  • Enrolled with a major cell phone carrier
  • Agree to verification of smoking cessation status by a significant other
  • Able to read and write in English
Both
18 Years to 25 Years
Yes
Contact information is only displayed when the study is recruiting subjects
United States
 
NCT01516632
R21CA135669, 5R21CA135669
No
Center for Innovative Public Health Research
Center for Innovative Public Health Research
  • Michigan State University
  • The University of Texas Health Science Center, Houston
  • National Cancer Institute (NCI)
Principal Investigator: Michele Ybarra, MPH PhD Center for Innovative Public Health Research
Center for Innovative Public Health Research
January 2012

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP