Smoking Clinical Trial
Official title:
Preventing Initiation of Smoking by Children
The purpose of this study is to determine whether an anti-smoking program for parents who smoke will lower the odds that their children will start smoking. The study will evaluate an activity-based program for parents and their children. The program is home-based and uses the mail for program delivery.
Youth whose parents smoke cigarettes are at high risk for early initiation of cigarette
smoking, and youth who first smoke cigarettes during childhood are at high risk for
subsequent addiction to tobacco. Parents influence their children's perceptions of the
prevalence of smoking, the acceptability of smoking, the accessibility of cigarettes, and
the personal and social consequences of smoking. All parents, including parents who smoke,
can engage in anti-smoking socialization, which may lower children's risk of smoking.
Although there are some programs available that are directed at preventing initiation of
smoking during childhood, none of these prevention programs engage parents who smoke in
altering children's smoking-specific socialization. This study will evaluate a program to
change smoking-specific socialization of children in households where parents smoke
cigarettes.
Consenting volunteers will be randomly assigned to either treatment (anti-smoking
socialization program) or control groups. Parents in the treatment group will participate in
the "Smoke-free Kids" program and receive activity magazines, newsletters, and support
calls. Parents in the control group will receive a fact sheet about youth smoking. Parents
involved in the study will be assessed through a telephone interview 1 month after
completion of the three-month anti-smoking program. Assenting children will complete surveys
administered at school at 12, 24, and 36 months after completion of the anti-smoking
program. Primary and secondary dependent variables include initiation of cigarette smoking
and susceptibility to cigarette smoking by children. The child survey will also assess risk
and protective factors.
;
Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Single Blind, Primary Purpose: Educational/Counseling/Training
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