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LA Sprouts: The Impact of Gardening and Nutrition Education on Childhood Obesity in Latino Youth

LA Sprouts: The Impact of Gardening and Nutrition Education on Childhood Obesity in Latino Youth

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02291146
Acronym
LA Sprouts
Enrollment
421
Registered
2014-11-14
Start date
2011-07-31
Completion date
2013-12-31
Last updated
2014-11-14

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Pediatric Obesity

Keywords

gardening, cooking, nutrition education, Hispanic Americans

Brief summary

The overall goal of this project is to conduct a randomized controlled 12-week after school, gardening, nutrition and cooking program (called LA Sprouts) to improve dietary intake and reduce obesity in 3rd, 4th and 5th grade students (ages 8-12 years) in Los Angeles. Approximately 400 3rd - 5th grade students participating in the LA's Best after school program will participate. Four elementary schools in Los Angeles will be selected to participate in the study. Schools will be randomized by region to either receive the intervention (LA Sprouts; 2 schools, n=200 students) or serve as controls (received a delayed intervention program one school semester later; 2 schools, n=200 students). The LA Sprouts intervention will take place at the elementary schools, with gardens on campus specially designed and built for this project. The program will be held once a week for 12 weeks and will consist of a 45-minute gardening lesson, taught by Master Gardeners from the University of California Cooperative Extension (supervised by Nicole Gatto, MPH, PhD), and a 45-minute nutrition education and cooking lesson, taught by USC a Nutrition Educator (supervised by Jaimie Davis, PhD, RD). Measures of childhood obesity (i.e., body mass index (BMI) and body fat percentages), blood pressure, metabolic function (fasting blood glucose, insulin and lipids), dietary intake and related behaviors, and school performance will be measured before and after the implementation of the program in both intervention and control participants. Approximately 10 additional students of the same age will be asked to participate in a focus group to evaluate the questionnaire developed for this study. In addition, approximately 20 additonal students of the same age will be asked to participate in a test-retest session to validate the reliability of the questionnaire.

Interventions

BEHAVIORALLA Sprouts intervention

see arm 1 description

Sponsors

Loma Linda University
CollaboratorOTHER
University of Texas at Austin
CollaboratorOTHER
University of California, Los Angeles
CollaboratorOTHER
National Institutes of Health (NIH)
CollaboratorNIH
Annenberg Foundation
CollaboratorUNKNOWN
University of Southern California
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
8 Years to 12 Years
Healthy volunteers
Yes

Inclusion criteria

* Normal, Overweight and Obese Children: Investigators will attempt to obtain a natural selection of normal weight children (age- & sex-specific BMI \< 85th percentile based on CDC BMI growth charts (40) and overweight and obese children (BMI ≥ 85th percentile). Based on preliminary data from these areas, investigators expect that at least 50% of the sample will be overweight or obese. There will not be an upper BMI limit. Gender & Age: Investigators will attempt to enroll equal numbers of female and male students in 3rd through 5th grades (8-12 years of age). Latino origin: This study will include all ethnicities, however the selected schools are \>90% Latino.

Exclusion criteria

* The following criteria are exclusionary: presently taking medication(s) or diagnosed with any disease that could influence dietary intake or body composition; previously diagnosed with any major illness since birth (e.g. chronic birth asphyxia, cancer, etc.); any physical, cognitive, or psychological disability that would prevent participation in the study. Participants testing positive for diabetes (as determined from the fasting blood draw) will be referred for treatment. (Note: subjects with pre-diabetes will be eligible for the study). Although participant data may be excluded based on the above

Design outcomes

Primary

MeasureTime frameDescription
change in adipositybaseline and 12 weeksmeasured by BMI, waist circumference, and body fat percentages (via Tanita scale)
change in blood pressurebaseline and 12 weeks
change in metabolic functionbaseline and 12 weeksmeasured by fasting glucose, insulin and lipids

Secondary

MeasureTime frameDescription
change in dietary intakebasline and 12 weeksmeasured via screener, specifically fruits, vegetables, fiber
change in determinants of fruit and vegetable intakebasline and 12 weeksmeasured via LA Sprouts questionnaire (developed for this study), ie knowledge, preferences, self-efficacy, motivation

Other

MeasureTime frameDescription
change in school engagementbasline and 12 weeksmeasured via LA Sprouts questionnaire (developed for this study)

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026