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Rural Disparities in Pediatric Obesity: The iAmHealthy Intervention

University of Kansas logo

University of Kansas

Status

Completed

Conditions

Weight Loss

Treatments

Other: Newsletter
Behavioral: iAmHealthy Healthy Lifestyles Program

Study type

Interventional

Funder types

Other
NIH

Identifiers

NCT03304249
iAmHealthy 2
R01NR016255-01A1 (U.S. NIH Grant/Contract)

Details and patient eligibility

About

The purpose of this study is to learn if providing a family-based group program using mobile health technology (iAmHealthy Healthy Lifestyles Program) is effective at improving child weight, nutrition, and physical activity.

Full description

This is a cluster-randomized study that will test the iAmHealthy Healthy Lifestyles Program versus a standard approach to weight loss in kids current in 2nd thru 4th grade. The iAmHealthy Healthy Lifestyles Program utilizes mobile tools to deliver the weight loss program to kids and families in rural settings. This study will include kids from schools in rural cities/counties, and their parents, and they will be randomly assigned to a group by their school.

The iAmHealthy Healthy Lifestyles Program is a rurally tailored telemedicine intervention. It delivers behavioral, nutritional, and physical activity topics for kids and their families. The total length of the intervention will be about 8 months, which coincides with the length of a typical school year.

Enrollment

296 patients

Sex

All

Ages

5 to 10 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Family lives in a rural area (city and/or county population less than 20,000)
  • Child Body Mass Index (BMI) >85th and <99th percentile
  • Child in 2nd thru 4th grade
  • Child and Parent speak English
  • Family is available at times intervention is offered

Exclusion criteria

  • Child has physical limitation or receives an injury which significantly limits physical mobility
  • Child has significant medical issue
  • Child and Parents have significant developmental delay or cognitive impairment
  • Child has a sibling who has already enrolled in the program
  • Family moves to a non-participating school

Trial design

Primary purpose

Prevention

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

296 participants in 2 patient groups

iAmHealthy
Experimental group
Description:
Participants randomized to this arm receive the iAmHealthy Healthy Lifestyles Program.
Treatment:
Behavioral: iAmHealthy Healthy Lifestyles Program
Control
Active Comparator group
Description:
Participants randomized to this group receive comparable content delivered via a newsletter.
Treatment:
Other: Newsletter

Trial documents
1

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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