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Clinical Trials/NCT01333241
NCT01333241
Completed
N/A

Community-Based Lifestyle Promotion With Latino Women

University of California, Los Angeles1 site in 1 country223 target enrollmentAugust 2009

Overview

Phase
N/A
Intervention
Not specified
Conditions
Cardiovascular Diseases
Sponsor
University of California, Los Angeles
Enrollment
223
Locations
1
Primary Endpoint
Change in Body mass index (BMI)
Status
Completed
Last Updated
6 years ago

Overview

Brief Summary

The overall goal of this randomized controlled trial is to evaluate the effects of a community-based lifestyle behavior intervention (LSBI) that is designed to improve dietary habits and physical activity (PA), and reduce weight of Latino women who are predominantly Spanish-speaking immigrants. It is hypothesized that middle-aged overweight/obese Latinas participating in a LSBI conducted by lay health advisors will demonstrate improved dietary habits, increased physical activity and a decrease in BMI compared to those in a control condition, Women in the LSBI also are expected to demonstrate improvements in selected physiologic outcomes (waist circumference, blood pressure [BP], measures of cholesterol and blood sugar).

Detailed Description

Overweight/obesity and physical inactivity are two significant predictors of illness and death from cardiovascular (heart) disease (CVD) in Latina adults. These risk factors may be reduced or eliminated through prevention efforts that focus on heart-healthy diets, weight reduction, and PA. The purpose of this study is to compare the effects of a 6-month community-based lifestyle behavior intervention (LSBI) conducted by lay health advisors and a control condition (disaster preparedness and home safety program) on lifestyle behaviors -dietary habits and physical activity(primary outcome) and selected physiologic outcomes (secondary outcomes) i.e., BMI, waist circumference, blood pressure, measures of cholesterol,and fasting blood sugar of Latinas who are overweight/obese. The LSBI includes group education (8 classes) and individual teaching and coaching (8 contacts by home visits and telephone calls) delivered over a 6-month period. Acceptability and feasibility of the intervention is evaluated through examination of women's retention rates and participation in classes and home visits.

Registry
clinicaltrials.gov
Start Date
August 2009
End Date
July 2012
Last Updated
6 years ago
Study Type
Interventional
Study Design
Parallel
Sex
Female

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Deborah Koniak-Griffin

Professor

University of California, Los Angeles

Eligibility Criteria

Inclusion Criteria

  • 35 to 64 years of age
  • body mass index (BMI) \>25
  • fluent in either Spanish or English.

Exclusion Criteria

  • pregnant or planning to get pregnant in next year
  • history of myocardial infarction or stroke
  • currently under treatment for cancer
  • orthopedic or joint problems that would prohibit participation in physical activity
  • insulin-dependent diabetes

Outcomes

Primary Outcomes

Change in Body mass index (BMI)

Time Frame: Baseline, 6 and 9 month follow-up.

Secondary Outcomes

  • Change in Physiologic measures(Baseline, 6 and 9 month follow-up.)
  • Change in Lifestyle behaviors(Baseline, 6 and 9 month follow-up.)
  • Change in Physical Activity(Baseline, 6 and 9 month follow-up)

Study Sites (1)

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