The Impact of a Parenting Intervention on Latino Youth Health Behaviors

NCT03517111 · Status: TERMINATED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 844

Last updated 2024-02-26

Study results available
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Summary

The purpose of this study is to test if a parenting program can be used to prevent substance use among Latino youth and at the same time promote healthy eating. Pairs of 7th grade students and one of their parents will be enrolled in the study and randomly assigned to three groups: an existing parenting intervention focusing on substance use prevention (FPNG), the enhanced parenting intervention that also has nutrition content (FPNG+), and a comparison program focused on academic success. Only parents will attend intervention sessions. Data will be collected from the parent and their 7th grade student to see how these programs impacted substance use, nutrition, and parenting. The investigators hypothesize that families receiving the FPNG+ will have improved nutrition habits than the other conditions. Students in both FPNG and FPNG+ will have lower substance use rates as compared to the academic success program. In addition, the effects of parenting strategies and sociocultural factors on the FPNG and FPNG+ results will be studied.

Conditions

  • Diet Modification
  • Substance Use Disorders
  • Diabetes Mellitus Risk
  • Cardiovascular Risk Factor
  • Lifestyle Risk Reduction
  • Parenting

Interventions

BEHAVIORAL

Nutrition/substance use prevention

Parenting program focusing on diet improvement and substance use prevention

BEHAVIORAL

Substance use prevention only

Parenting program focusing only on substance use prevention

BEHAVIORAL

Academic success program

Program focusing on academic success and college acceptance

Sponsors & Collaborators

  • National Institute on Minority Health and Health Disparities (NIMHD)

    collaborator NIH
  • Arizona State University

    lead OTHER

Principal Investigators

  • Flavio F Marsiglia, PhD · Southwest Interdisciplinary Research Center, Arizona State University

Study Design

Allocation
RANDOMIZED
Purpose
PREVENTION
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
12 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2018-09-26
Primary Completion
2022-03-31
Completion
2022-03-31

Countries

  • United States

Study Locations

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Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT03517111 on ClinicalTrials.gov