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Clinical Trials/NCT05858580
NCT05858580
Active, Not Recruiting
N/A

Pilot Study of a Home-based Program to Promote Healthy Diet and Activity in Rural-dwelling Children

Wake Forest University Health Sciences1 site in 1 country60 target enrollmentMarch 1, 2024

Overview

Phase
N/A
Intervention
Not specified
Conditions
Obesity, Childhood
Sponsor
Wake Forest University Health Sciences
Enrollment
60
Locations
1
Primary Endpoint
Change in Fruit and Vegetable Intake (carotenoid concentration) at 7 months
Status
Active, Not Recruiting
Last Updated
4 months ago

Overview

Brief Summary

The study proposes a randomized pilot and feasibility study of a lifestyle modification program to promote healthy diet and activity in rural-dwelling children to reduce Type 2 Diabetes risks.

Intervention participants will receive 6 months of programming to include:

  • 16 activity packs;
  • 9 health coach sessions;
  • unlimited access to a resource toolbox.

Control participants will receive 6 activity packs promoting science, technology, engineering, and math (STEM) learning and 6 check-in calls to support retention.

Detailed Description

The rising prevalence of obesity and type 2 diabetes (T2D) at increasingly younger ages compels development of new strategies to combat these preventable conditions. Healthy diet and activity are critical to reducing risk, yet these behaviors decline starting in childhood. These trends are most troubling in rural areas, where youth consume more calories and sugar-sweetened beverages but less fruit and whole grains; engage in less physical activity; and are more likely to have overweight or obesity than urban peers. Given unhealthy behaviors are set by adolescence, promoting healthy diet and activity in rural children is crucial to reducing rural-urban disparities in obesity and T2D across the lifecourse. The investigators have developed a multi-component, family-based intervention to improve diet and activity in children at risk of youth-onset obesity and T2D. The pilot study will gather necessary and sufficient data on feasibility, acceptability, and effect size to finalize the design of a clinical trial. The investigators will recruit 60 English- or Spanish-speaking children in 2nd to 5th grades from rural communities in Colorado or North Carolina. Participants will be randomized to 6 months of intervention or control programming. Intervention participants will receive approximately 25 hours of programming over 6 months through a) 16 self-contained, parent-guided activity kits, b) 9 one-on-one health coach/support sessions in-person or virtual by a trained health coach, and c) unlimited access to a resource toolbox. Control participants will receive 6 activity kits promoting science, technology, engineering, and math (STEM) learning and will receive 6 check-in calls to support retention. Standardized measures will be collected at 0 and 7 months. Qualitative interviews will also be conducted at 7 months. Process measures will be tracked by staff throughout the study. With positive results, this innovative pilot study will form the foundation of a clinical trial to evaluate the sustained impact of an at-home, family-based intervention to promote diet and activity in rural children, which can subsequently be disseminated and implemented among the 13 million children living in rural US settings and reduce T2D risks.

Registry
clinicaltrials.gov
Start Date
March 1, 2024
End Date
March 1, 2026
Last Updated
4 months ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • 7-to-10-years-old
  • Living in rural Colorado or rural North Carolina
  • English- or Spanish-speaking
  • Has 1 parent or primary caregiver willing to actively participate

Exclusion Criteria

  • Medical diagnosis of diabetes
  • Serious child or parent health concerns that would interfere with participation
  • Plans to move out of the area during the study period
  • Lives with another child who previously participated in the study

Outcomes

Primary Outcomes

Change in Fruit and Vegetable Intake (carotenoid concentration) at 7 months

Time Frame: Month 7

Use the Veggie Meter (Longevity Link, Salt Lake City, UT) to assess carotenoids, a biomarker of fruit and vegetable intake. The device estimates total dermal carotenoid concentration by illuminating the fingertip with a blue wavelength laser light and detecting vibrational/rotational energy levels of molecules, correcting for hemoglobin and melanin levels.

Change in Sugar-Sweetened Beverage Intake (carbon isotope ratio) at 7 months

Time Frame: Month 7

Collect red blood cells to measure the carbon isotope ratio, a biomarker of sugar-sweetened beverage intake. Samples will be analyzed via continuous-flow isotope ratio mass spectrometry at the University of Alaska Stable Isotope Facility.

Change in Dietary Intake (MyPyramid Equivalents) at 7 months

Time Frame: Month 7

Diet will be assessed with 24-hour dietary recalls using the Automated Self Administered system (ASA24). This system uses the USDA multiple-pass method to query all foods and supplements consumed in the prior 24 hours and produces daily and individual food estimates for macronutrients, micronutrients, and MyPyramid Equivalents (such as servings of vegetables, fruits, whole grains, solid fats, and added sugars).

Secondary Outcomes

  • Change in Screen Time at 7 months(Month 7)
  • Change in Physical Activity at 7 months(Month 7)

Study Sites (1)

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