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Clinically Tested

SmokeSignals quit plans are built on principles of Scheduled Reduction. The scheduling of cigarettes has proven even more important than the reduction of cigarettes1. By removing smokers’ discretion, they do not give up only low preference cigarettes2 and must balance their usage throughout the day – sometimes having to smoke at inconvenient times that create negative associations, and sometimes missing the chance to smoke during their usual pleasurable situations.

Research shows that successful smoking cessation and relapse avoidance require behavioral changes, and relearning takes time . Over the 4-8 week regimens, smokers learn many coping skills and practice them hundreds of times. This preparation for quitting is paramount to preventing relapse, which sadly concludes most quit attempts within 7 days.

The process of scheduled gradual reduction titrates nicotine evenly throughout the day. Nicotine fades so gradually and is dosed so evenly through the day that quitters experience fewer withdrawal symptoms or urges3 . Cravings that would normally trigger relapse are reduced when nicotine intake is spaced smoothly throughout the day.

Quit rates have been exceptionally high with tailored reduction; urges and withdrawal symptoms have been minimized and relapse rates have been lower in several published academic studies. Dr. Paul Cinciripini and colleagues, in pioneering trials at M.D. Anderson Cancer Center, developed this breakthrough regimen, achieving 70%+ quit rates in two trials with 44% remaining smoke free a year later.

Dr. Albert Jerome and colleagues working with early-stage hand-held computers for smoking cessation implemented these principles in the LifeSign device from the mid 1980’s. They reported abstinence rates of 13% to 24% in self-help studies4 and quit rates as high as 36% when used with therapist assistance5.

Three randomized controlled trials have been conducted on SmokeSignals®, supported by NIDA and NCI SBIR funding. Our first efficacy clinical trial yielded 36.4% abstinence among device-using participants vs. 0% of the control group not using the device.

In a Harm Reduction trial aimed at resistant quitters willing to reduce by half for five weeks, 49.5% of all enrollees (n=47) met or exceeded weekly goals. Importantly, two-thirds of the completers (21/ 33) opted to move on to cessation regimens at Week 6, and two-thirds of those attempts (16) -- a third of the original pool of resistant quitters) demonstrated abstinence.

A third recent trial compared a group paced by our compliance adjusting algorithms to a group paced on a three-week fixed schedule. The Adjusting group demonstrated a significantly higher post-treatment bio-chemically validated 7-day point prevalence abstinence rate (45.2% vs. 22.2%, SE = 9.3%; F = 102.74, p < 0.01), was more compliant, and showed greater dependence reduction. When left to find their own natural duration to cessation, the Adjusting group averaged 5. 5 weeks.

Two other long-term studies are in process and will be published next year.


  1. Cinciripini, P.M., Wetter, D.W., McClure, J.B., (1997), Scheduled Reduced Smoking: Effects on smoking abstinence and potential mechanisms of action. Addictive Behaviors, 22, 6, 759-767
  2. Pomerleau, O.F., & Pomerleau, C.S. (1984), Neuroregulators and the reinforcement of smoking: Towards a biobehavioral explanation. Neuroscience & Biobehavioral Reviews, 8, 503-513
  3. Cinciripini, P.M., Lapitsky, L.G., Seay, S., Wallfisch, A., Kitchens, K., and Van Vunakis, H. (1995). The effects of smoking schedules on cessation outcome: Can we improve on common methods of gradual and abrupt nicotine withdrawal. , Journal of Consulting and Clinical Psychology, 63, 388-399
  4. Prue, D.M., Riley, A., Orlandi, M.A., Jerome A. (1990). Development of a computer-assisted smoking cessation program: A preliminary report. Journal of Advancement in Medicine, 3(2), 131-139.
  5. Jerome, A., Perrone, R., & Kalfus G. (1992). Computer-assisted smoking treatment: A controlled evaluation and long-term follow-up. Journal of Advancement in Medicine, 5

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