CommunityAHFCommunity-Based Obesity Treatment for Latino Children in Immigrant Families
This study aims to provide a community-based obesity treatment for Latino children in immigrant families, observing changes in their BMI category and %BMIp95 before and after the program.
Community Active and Healthy Families
Body Weight+6
+ Nutrition Disorders
+ Nutritional and Metabolic Diseases
Treatment Study
Summary
Study start date: March 13, 2023
Actual date on which the first participant was enrolled.This study, Community Active and Healthy Families (AHF), aims to tackle childhood overweight issues among Latino children from immigrant families. The focus is on 5-12 year olds who are overweight or obese. The goal is to test a community-based obesity treatment program, with the hope of reducing disparities in childhood overweight within this population. This research is important as it could pave the way for more effective care and address the current challenges faced by this specific group. During the study, participants will engage in the Community-AHF program. The progress of each child is measured by changes in their %BMIp95, which is a calculation based on their age, sex, and Body Mass Index. This measurement is taken at the beginning and end of the active phase of the Community-AHF program. As this is a pilot study, it's not designed to show statistically significant differences before and after the intervention. Instead, the data collected will be used to test hypotheses and help plan for a larger, more comprehensive study in the future. The study will analyze data from participants who provide measurements both before and after the program to avoid any potential biases.
Protocol
This section provides details of the study plan, including how the study is designed and what the study is measuring.78 patients to be enrolled
Total number of participants that the clinical trial aims to recruit.Treatment Study
Eligibility
Researchers look for people who fit a certain description, called eligibility criteria: person's general health condition or prior treatments.Any sex
Biological sex of participants that are eligible to enroll.From 5 to 99 Years
Range of ages for which participants are eligible to join.Healthy volunteers not allowed
If individuals who are healthy and do not have the condition being studied can participate.Conditions
Pathology
Criteria
Study Plan
Find out more about all the medication administered in this study, their detailed description and what they involve.One single intervention group is designated in this study
This study does not include a placebo group
Treatment Groups
Group I
ExperimentalStudy Objectives
Primary Objectives
Secondary Objectives
Study Centers
These are the hospitals, clinics, or research facilities where the trial is being conducted. You can find the location closest to you and its status.This study has 2 locations
Johns Hopkins University
Baltimore, United States