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Project humAn dieTary daTa rEtuRN

Effects of Diet Data Return on Human Dietary Patterns

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06266689
Acronym
PATTERN
Enrollment
600
Registered
2024-02-20
Start date
2024-02-27
Completion date
2026-12-01
Last updated
2026-01-29

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

Conditions

Diet Habit

Brief summary

This study is designed to test the effects of diet data return on human dietary patterns. The investigators' working hypothesis is that returning diet data, collected via an empirical biomarker-based assessment method, will promote participant eating behavior changes towards a more healthful diet, and that these dietary patterns may also be reflected in the structure and function of the gut microbiome and in participant health outcomes. Here, the investigators will explore this hypothesis with participants supplying stool (poop) samples that will be used to assess their diet using the investigators' DNA-biomarker based method. Participants will have their diet data returned to them, and will then supply post-intervention stool samples for dietary assessment to investigate the efficacy of diet data return in impacting subject dietary patterns and health. It is anticipated that the investigators will enroll infants, children, and adults across the age span, including infants that are currently participating in Project HOPE 1000, a longitudinal observational study of mothers and infants from pregnancy through early childhood (Pro00100000). This study represents a minimal risk to subjects; namely, the potential loss of privacy involved with study participation.

Interventions

BEHAVIORALPersonalized Diet Information

These participants will receive a report detailing their genomic food data based on the investigators' DNA metabarcoding technique in addition to standard dietary guidance to see if receiving the report modifies what they choose to feed their infant.

Sponsors

Duke University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
OTHER
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
No minimum to 12 Months
Healthy volunteers
Yes

Inclusion criteria

* Participant's parent/legal guardian is over age 18 and able to understand English * Plans to remain in the area for the next two years * Primary caregiver for infant less than 12 months old * Able to collect and ship the requested infant stool samples

Exclusion criteria

There will be no specific exclusions for this study. However, the following biospecimens will not be collected for research purposes from individuals who have a condition that, in the opinion of the site investigators and/or providers, would place the subject at unacceptable risk of injury or confound data interpretation; including but not limited to: * Health conditions that impact the infant feeding in a way that may confound interpretation of study results.

Design outcomes

Primary

MeasureTime frameDescription
Number of participants with diet improvement12 monthsThe investigators' primary objective is to test the hypothesis that returning DNA metabarcoding data is an effective method for improving diet and increasing dietary diversity.
Number of participants with increased dietary diversity12 monthsthe investigators' primary objective is to test the hypothesis that returning DNA metabarcoding data is an effective method for improving diet and increasing dietary diversity.

Secondary

MeasureTime frameDescription
Number of participants with changes in the composition and function of the gut microbiome12 monthsAssess whether dietary diversity is associated with the structure and function of the gut microbiome and health outcomes.

Countries

United States

Contacts

CONTACTLawrence A David, PhD
lawrence.david@duke.edu(919) 668-5388
CONTACTKirsten Jenkins, B.S
kirsten.jenkins@duke.edu9196684736

Outcome results

None listed

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