Cardiovascular Diseases Clinical Trial
To conduct a cross-sectional study of cardiovascular risk factors in a cohort of Latina women.
BACKGROUND:
Cardiovascular disease (CVD) is the leading cause of death among Latina women (LW) in the
United States. Nursing knowledge in the area of CVD and Latina women is currently
underdeveloped. Most studies have included Mexican women with limited information on how
predictors such as resources, situational, personal, and demographic factors have an effect
on the CVD-related dietary practices, physical activity, and exercise practices among Latina
women subgroups such as Central American women.
DESIGN NARRATIVE:
To conduct a cross-sectional and follow-up preliminary intervention study in order to
describe and analyze the CVD-related diet, physical activity, and exercise practices
predictors in 221 Mexican and Central American women recruited from six counties in Northern
California. Face-to-face interviews were conducted with Mexican American and Central
American women (ages 40-75) who had at least one risk factor for CVD to answer the following
questions: What were the CVD-related risk factors, dietary practices, physical activity, and
exercise behaviors in Mexican and Central American women who were 40 to 75 years and who had
at least one risk factor for CVD? What was the relationship between predictor variables
(resources, situational, personal, and demographic factors) with CVD-related diet practices,
physical activity, and exercise behaviors (outcome variables)?, and what were the short and
intermediate-term effects of a cardiovascular nursing intervention on diet, physical
activity, and exercise? A sample of 221 women was targeted. Data were collected during the
first two years of the project to provide substantial research-based information to develop
a cardiovascular nursing intervention to support Latina women efforts to promote heart
health and prevent CVD. Data were analyzed during the third year and the cardiovascular
nursing intervention was developed to determine the short (3 months) and intermediate-term
(6 months) effects in the outcome variables. A randomly selected sample of 60 women from the
same cohort was randomly assigned to the developed intervention group (n=30 in each group)
and to a delayed-intervention control group.
The study completion date listed in this record was obtained from the "End Date" entered in
the Protocol Registration and Results System (PRS) record.
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