Effects of behavioral and pharmacological treatment on smokeless tobacco users

J Consult Clin Psychol. 1996 Feb;64(1):153-61. doi: 10.1037//0022-006x.64.1.153.

Abstract

The purpose of this study was to examine the effects of 2 mg of nicotine polacrilex versus placebo gum and of group behavioral treatment versus minimal contact on cessation of smokeless tobacco use. Participants (N = 210) were randomly assigned 1 of the 4 treatment conditions. Withdrawal symptoms were assessed throughout the treatment. Follow-up assessments were made at 1, 6, and 12 months posttreatment. Survival curve analysis showed that any of the 3 treatment groups involving group behavioral therapy or placebo gum were equally effective and superior to the minimal contact plus 2 mg of nicotine gum treatment in terms of abstinence. On the other hand, withdrawal symptoms were significantly reduced by nicotine gum, compared with placebo during the initial phases of cessation. The ineffectiveness of nicotine gum on treatment outcome may be attributed to its similarity with smokeless tobacco.

Publication types

  • Clinical Trial
  • Comparative Study
  • Randomized Controlled Trial
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Adult
  • Behavior Therapy*
  • Chewing Gum
  • Follow-Up Studies
  • Humans
  • Male
  • Nicotine / administration & dosage*
  • Plants, Toxic*
  • Psychotherapy, Group
  • Survival Analysis
  • Tobacco Use Disorder / psychology
  • Tobacco Use Disorder / rehabilitation*
  • Tobacco, Smokeless*
  • Treatment Outcome

Substances

  • Chewing Gum
  • Nicotine