Obesity Clinical Trial
This study addresses the high risk of weight gain associated with smoking cessation in women. The obesity prevention pilot study is designed for the primary prevention of weight gain that can lead to overweight in normal-weight women, that can progress to obesity in women who are already overweight, and for the prevention of additional weight gain in obese women with BMI greater than or equal to 30.0. Fat and other macronutrient intake, specifically, sugar, complex carbohydrates, and protein, are analyzed as a target for individually tailored, weight control intervention following smoking cessation in Caucasian and African American women.
Middle-aged women, especially African Americans, who quit smoking are at high risk for
weight gain, overweight, and obesity. Postcessation weight gain has been attributed to
increased food intake, which in turn, has been ascribed to a selective increase in
high-sugar and other high-carbohydrate foods with a high-fat content. This study compares
the relative effectiveness, for postmenopausal Caucasian and African American women, of
following an empirically validated smoking cessation program with either 1) a group
cessation maintenance program with standard exercise advice and food pyramid instructions
for healthy eating or 2) an individually tailored, dietary-control, exercise,
weight-management and cessation-maintenance program. Effectiveness is assessed by weight
change from baseline to postcessation months 6, 12, and 20.
The second aim is to assess overall fat and other specific macronutrient intake (sugar,
complex carbohydrates, and protein) and total caloric intake with the use of a novel
macronutrient self-selection paradigm in Caucasian and African-American postmenopausal women
at baseline prior to smoking cessation, after being abstinent for one week, and again at 6,
12, and 20 months postcessation.
The third aim is to assess whether there is differential responsiveness on the above
measures in postmenopausal Caucasian vs. African-American women.
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Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Single Blind, Primary Purpose: Prevention
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