Skip to content

Diet and Microbiome Longitudinal Monitoring With Food Intervention

Diet and Microbiome Longitudinal Monitoring With Food Intervention

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04758715
Enrollment
65
Registered
2021-02-17
Start date
2021-02-02
Completion date
2030-02-28
Last updated
2026-05-07

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

Conditions

Gastrointestinal Tract, Microbiome, Human

Brief summary

The main goal of this project is to identify the microbiome components change in abundance in response to food ingested including provided foods.

Interventions

OTHERFood provided from a commercial meal service provider for a week

Meals from a commercial meal service provider provide for a week to participant

Sponsors

University of Nebraska Lincoln
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
BASIC_SCIENCE
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
19 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

* willing to sign consent and have samples collected, * able to read and speak English, * participants must be willing to use an electronic food diary and consume study provided foods, * only individuals able to provide a US address will be included.

Exclusion criteria

* Subjects not able to sign consent on their own accord (ie requiring a Legally Authorized Representative \[LAR\]), * Current parenteral nutrition, * Received cancer treatment within past 6 months prior to signing consent, * Taken antibiotic treatment within the past 1 month prior to signing consent, * Received oral x-ray contrast within the past 1 month prior to signing consent, * Received any type of gastrointestinal bowel preparation in the past 1 month prior to signing consent, * History of organ transplant, * Shellfish allergy, * Insect allergy, * Cacti allergy, * Carmine allergy, * Dragon fruit (pitaya) allergy,

Design outcomes

Primary

MeasureTime frameDescription
Microbiota variationUp to 2 weeksEcological statistics will be used to analyze the longitudinal microbiome composition modification

Countries

United States

Contacts

PRINCIPAL_INVESTIGATORJacques Izard, PhD

Univeristy of Nebraska-Lincoln

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: May 8, 2026