PT - JOURNAL ARTICLE AU - Gala, S AU - Pesek, F AU - Murray, J AU - Kavanagh, C AU - Graham, S AU - Walsh, M TI - Design and Pilot Evaluation of an Internet Spit Tobacco Cessation Program DP - 2008 Jan 01 TA - American Dental Hygienists Association PG - 11--11 VI - 82 IP - 1 4099 - http://jdh.adha.org/content/82/1/11.short 4100 - http://jdh.adha.org/content/82/1/11.full SO - J Dent Hyg2008 Jan 01; 82 AB - Purpose. To develop an interactive Web site to help smokeless tobacco (ST) users to reduce or stop their ST use and pilot test it for feasibility, acceptability, and short-term outcomes. Methods. An interactive, multiple-contact Internet ST cessation program was developed, refined based on feedback from 17 ST users, and pilot-tested for feasibility, acceptability, and short-term effects on the ST-related behavior and attitudes among baseball athletes attending 3 colleges in California. Consenting ST users completed a baseline questionnaire and enrolled on the Web site for help with stopping ST use. One month later, outcomes were assessed. Results. Although 18 ST-using baseball athletes enrolled on the Web site, follow-up data were obtained from 12 individuals. Loss to follow-up occurred when we were unable to contact participants by telephone or mailed surveys. At 1-month follow-up, over 80% (N=11) reported that the Web site was: “helpful in stopping or reducing my tobacco use”; easy to navigate; and “appealing.” Moreover, 8% (n=1) self-reported abstinence from ST use. Among nonquitters, there was a 26% mean reduction in ST use per day compared to baseline values. In addition, among all enrollees, there was a 4-fold increase in motivation to quit (7% versus 31%) and a 21% increase in their confidence in being able to quit (67% versus. 85%) from baseline to follow-up. Conclusion. The interactive ST cessation Web site was feasible to implement, acceptable to ST users, and appeared to reduce ST use, enhance motivation to quit, and increase confidence about one's ability to quit. Further study with a larger sample size and a control group is needed to determine efficacy to promote cessation of ST use.