Smoking Cessation Clinical Trial
Official title:
Intervention for Support Persons to Help Smokers Quit
This study will examine the feasibility and potential effectiveness of an intervention for adults who want to help support a smoker to quit. The support persons will receive either self-help materials only or the self-help materials plus a telephone counseling intervention. Both interventions provide information on how support persons can encourage a smoker to quit.
Interventions that reach the majority of cigarette smokers in the population have the
greatest potential to impact the public health. Most smokers do not seek treatment for
smoking cessation. A novel behavioral approach to reaching smokers is to directly recruit
and train adult nonsmokers to intervene (i.e., support persons). Several studies provide
evidence for the role of social support in smoking cessation. The use of support persons as
change agents for smoking cessation represents a shift from conventional interventions that
focus almost exclusively on the smoker. This proposal builds on our previous work that
indicates a skills training intervention for support persons is feasible and acceptable to
participants. Moreover, the effect size observed for the smoking abstinence rate in the
smokers, as reported by the support persons, provides some evidence of potential efficacy.
However, the intensive, group, clinic-based format of the intervention limits its potential
dissemination. We propose to develop and pilot test a more streamlined version of the
intervention using a telephone-based format. To enhance internal validity of the findings,
additional formative work is also needed to examine the feasibility of obtaining baseline
assessments and outcomes directly from the smoker. Social cognitive theory is the conceptual
basis for the proposed intervention.
The objective of this R21 proposal is to develop and pilot test a novel behavioral approach
to smoking cessation that utilizes support persons in the smoker's natural environment. We
expect that as a result of this project, we will have developed a well-specified and
feasible telephone counseling intervention, the efficacy of which can be tested in future
larger-scale randomized clinical trials.
This project will take place in two phases. In Phase 1, we will develop a telephone
counseling intervention for support persons, adapting and refining the intervention from our
previous, clinic-based treatment study. During this phase, we will develop the telephone
counselor manual, and 10 support persons will complete the protocol, which will be modified
and refined based on feedback from participants and counselors. Phase 2, consisting of a
pilot clinical trial, will apply a randomized, two group design with repeated assessments at
weeks 0 (baseline), 10 (end-of-treatment), and 26. Support persons (N=60) will be recruited
and randomly assigned to self-help intervention or telephone counseling. The smokers will be
enrolled as study subjects but will be contacted for assessments only.
;
Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment
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