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Early Childhood Obesity Among Rural Residents of West Texas

Reason given: Enrollment issues

Key facts

Where
Lubbock, United StatesSee the site

Where in United States

  • Texas Tech University Health Sciences CenterLubbock, United StatesNo longer taking part

Trial details

Who runs it
Texas Tech University Health Sciences Center
Trial code
NCT06831097
Record updated
29 June 2026
Original description
The Para Salud study is a longitudinal, community-based participatory research (CBPR) initiative aimed at preventing and controlling obesity among preschool children in rural Texas. The study will implement evidence-based interventions targeting nutrition, physical activity, and gardening. The interventions are designed to improve health outcomes, specifically in reducing obesity-related metrics among young Hispanic children, who are at a higher risk of obesity due to social determinants of health.Read full original descriptionShow less

The Para Salud study is a longitudinal, community-based participatory research (CBPR) initiative aimed at preventing and controlling obesity among preschool children in rural Texas. The study will implement evidence-based interventions targeting nutrition, physical activity, and gardening. The interventions are designed to improve health outcomes, specifically in reducing obesity-related metrics among young Hispanic children, who are at a higher risk of obesity due to social determinants of health.

Primary Objective: To assess the effectiveness of the Para Salud interventions in reducing obesity-related metrics, including BMI percentile, waist-to-height ratio, and percentage body fat, among preschool children aged 3-4 years in the Texas High Plains over a 24-month period.

Secondary Objective: To evaluate the impact of the Para Salud interventions on increasing physical activity levels, improving dietary habits (such as increasing fruit and vegetable intake), and reducing sedentary behavior and sugar-sweetened beverage consumption among the study participants.

Inclusion: Enrolled in the participating HS programs,; Aged 3-4 years,; Live in a selected county in Texas High Plains (Crosby, Floyd, Garza, Hale, Hockley, Lamb, Lubbock, Lynn, and Terry County); Without a diagnosed physical or mental disability according to enrollment records,; Parental consent; The inclusion criteria will be verified through children's enrollment records and the demographic information sheet. The parental/guardian participants will be the primary caregiver of each participating child, who lives in the same household of the child.

Exclusion: Health Status: Children with diagnosed physical or mental disabilities according to enrollment records; Lack of Consent: Children without parental/guardian consent to participate in the study.

ClinicalTrials.gov NCT06831097