Skip to content

Diet, Nutrient Status, and Food Insecurity

The Effect of Dietary Supplementation on Nutrient Status in Families Living in a Food Insecure Environment

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03412825
Enrollment
50
Registered
2018-01-26
Start date
2017-12-01
Completion date
2018-11-30
Last updated
2019-04-26

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Food Insecurity

Brief summary

Arkansas has one of the highest rates for food insecurity and 27.7% of children in the University of Arkansas area are food insecure. In addition, more than 14% of children ages 2-4 are obese and 20% of children ages 10-17 are obese. In Northwest Arkansas, the area surrounding the University of Arkansas in Fayetteville (Washington County), the food insecurity rate for adults is 17.9% (an estimated 34,730 individuals) and the food insecurity rate for children under 17 years of age is 24.4% (12,150 individuals). In addition, the surrounding counties have similar food insecurity rates (This makes Northwest Arkansas an ideal location to conduct a pilot study focusing on egg supplementation, childhood obesity, and food insecurity (http://www.feedingamerica.org/hunger-in-america/our-research/map-the-meal-gap).

Interventions

DIETARY_SUPPLEMENTEgg supplementation

Participants will required to consume 2 eggs per day, 5 days a week (a total of 10 eggs per week).

Sponsors

University of Arkansas, Fayetteville
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
BASIC_SCIENCE
Masking
DOUBLE (Subject, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
7 Years to 100 Years
Healthy volunteers
Yes

Inclusion criteria

* Food insecurity assessed by use of SNAP benefits or qualifying using the US Food Security Scale).

Exclusion criteria

* No dietary restrictions * Fear of needles * Metabolic disorders * Picky eating * Taking medication

Design outcomes

Primary

MeasureTime frameDescription
Micronutrient status in plasmaThe change in micronutrient status (e.g. iron, vitamin A, vitamin B12) will be measured from baseline to 16 weeks to determine if the dietary intervention improves baseline micronutrient status.Micronutrients status will be measured using plasma samples.
Body compositionThe change in body composition (e.g. ratio of lean to fat mass) will measured from baseline to 16 weeks.Body composition will be measured using dual X-ray absorptiometry (DEXA) .

Secondary

MeasureTime frameDescription
HeightThe change in height will be measured from baseline to 16 weeks.Height (in centimeters) will be measured using a stadiometer.
WeightThe change in weight will be measured from baseline to 16 weeks.Weight (in kilograms) will be measured using a scale.
Waist-to-hip ratioThe change in waist-to-hip ratio will be measured from baseline to 16 weeks.Waist-to-hip ratio will be measured using the protocol outlined by the World Health Organization.

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026