SBIR/STTR Research Award

Computerized SGR for Smoking Reduction

Award identifier f2e59684e994c996f913c6e1caae640e9ee5a40502de4379f51eb444f5f770a7Awarding agency Department of Health and Human Services · National Institutes of Health

Award amount

$391,539

Program and phase

SBIR · Phase II

Award year

2001

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Award details

Awarding agency
Department of Health and Human Services
Branch
National Institutes of Health
Recipient company
PERSONAL IMPROVEMENT COMPUTER SYSTEMS
Proposal award date
Not reported
Contract end date
Not reported
UEI
Not reported
Solicitation number
Not reported
Topic code
Not reported

Research abstract

DESCRIPTION (provided by investigator): The overall goal of this project is to continue development and evaluation of a self-help behavioral smoking reduction program for chronic smokers. The program, LifeSign for Smoking Reduction (LS-SR), is targeted to chronic smokers who are unwilling to quit smoking, and for whom a reduction in smoking is a reasonable short-term goal. In Phase I, we developed a prototype of the LS-SR program that used scheduled gradual reduction principles to reduce smoking by 50 percent and maintain these reductions, successfully recruited 99 smokers appropriate for a smoking reduction intervention, and assessed the feasibility of this prototype in a randomized controlled trial comparing LS-SR to a manually-guided research trial. The LS-SR condition produced greater, frequently significantly greater reductions, in various measures of smoking behavior, dependence, and nicotine exposure. For Phase II, we propose to modify the LS-SR program based on the Phase I results and compare this programs to a manually-based smoking reduction condition in 375 smokers who are not amenable to quitting smoking. Subjects will be randomly assigned to one of these self-help interventions and will be assessed at pre-intervention, at post-intervention 7 weeks later and at 14 and 28 weeks post-interventions. The primary outcome measure for the study will be 7 day reconstruction of daily smoking rate corroborated by CO and saliva cotinine assessment. CO and measures of short-term changes in health status (e.g. BP, and exertion, health status questionnaire.) Physical fitness will be measured at all assessment points. To determine the effect of smoking reduction on subsequent quit attempts, reported quit attempts, methods of quitting, and periods of abstinence (biochemically validated) as well as self-efficacy to quit and Stages of Change will be assessed at all visits. Additionally, measures of smoking typography will be obtained to measure directly the degree of compensatory smoking resulting from reduced smoking. PROPOSED COMMERCIAL APPLICATION: Not Available

Technology keywords

Not reported

Agency intelligence

Department of Health and Human Services

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