Skip to main content
OpenTrials
Completed

NCT Number: NCT05986955

The Impact of Food on Gut Microbiome Composition - a Clinical Trial Determining the Influence of Diet in Gut Microbiome Colonisation and Host Health

The goal of this clinical trial is to examine the impact of food derived bacteria on gut microbiome composition and host health. The main questions it aims to answer are:

* what is the the rate of gastrointestinal colonisation of food derived bacteria? * what is the contribution of food derived bacteria to gut microbiome stability?

Participants will complete a cross over feeding study of dietitian designed meals of known microbial load and will be asked to provide stool and blood samples for analysis.

Completed

Looking for future studies?

Notify Me

Key information

Conditions

Age range

18 year–65 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Early Phase 1

Primary location

BASE Facility

Notting Hill, Victoria, 3168, Australia

About this study

To understand the role and stability of food derived bacteria in impacting microbiome composition, 20 healthy participants will be recruited for this single site double blinded randomised controlled crossover pilot trial. The study is divided into four 14 day diet phases - baseline habitual, specified diet 1, habitual washout and specified diet 2. Participants will be randomly assigned to receive a microbial or non-microbial diet in specified diet 1 phase. Each participant will then crossover to receive the alternative diet in the specified diet 2 phase. The microbial and non-microbial diets will be identical except for the removal of naturally occurring food derived bacteria in non-microbial diet. At the commencement of the study and at the end of each diet phase, participants will attend a research clinic to undergo comprehensive clinical and anthropometric assessment and dietary evaluation.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Have no genetic conditions (e.g. Prader Willi or Down's Syndrome)
  • Not diagnosed with a significant medical conditions (e.g. irritable bowel syndrome, inflammatory bowel disease or type 1/2 diabetes)
  • Do not require drug-therapy (e.g. steroids or insulin or antibiotics)
  • Not taking dietary supplements, probiotics, prebiotics, symbiotics or fibre supplementation
  • Any condition that will affect participation in the study
  • Not pregnant, planning a pregnancy or breastfeeding
  • Able to complete a two-month dietary study and agree to eating all meals provided
  • Have no dietary allergies or dietary restrictions that prevent consumption of provided study meals
  • Open bowels regularly - mostly daily
  • Able to read, write and understand English

Exclusion criteria

  • Dietary concerns identified by dietitian
  • Aged less than 18 years and older than 65 years
  • Diagnosed with a medical condition that requires drug therapy
  • Taking medications or supplements known to alter gastrointestinal microbiota
  • Women who are pregnant, planning a pregnancy or breastfeeding
  • Anyone with a diagnosed gastrointestinal condition/disease e.g. irritable bowel syndrome or inflammatory bowel disease
  • Known dietary allergy and/or intolerance, follows a vegan or vegetarian diet, or has coeliac disease
  • Anyone with a preference for specific food avoidance or exclusion of certain ingredients in habitual diet
  • Unable to tolerate blood collection procedures
  • Unable to provide regular stool samples throughout the study

Treatment and study plan

Diet

Other

Participants will be assigned prospectively to microbial or non-microbial diet for first phase of trial and will then cross over to the alternate diet following a washout period.

Primary outcomes

  1. Characterisation of gut microbiome

    Time frame: Day 1, 4, 7, 11 and 14 of each phase

    Sequencing and bacterial culturing of stool samples

Secondary outcomes

  1. Participant body mass index (BMI)

    Time frame: BMI will be calculated on day 14 (at end of each diet phase (fortnightly))

    Assessed independently using height and weight measurements and appropriate formula

  2. Participant standing height

    Time frame: Height will be measured on day 14 (at end of each diet phase (fortnightly))

    Measured by stadiometer

  3. Participant weight

    Time frame: Weight will be measured on day 14 (at end of each diet phase (fortnightly))

    Measured using balance scales

  4. Participant waist circumference

    Time frame: Baseline day 1 and end of each 14-day diet phase

    Measured using standard measuring tape

  5. Participant Hip circumference

    Time frame: Baseline day 1 and end of each 14-day diet phase

    Measured using standard measuring tape

  6. Resting systolic and diastolic blood pressure

    Time frame: Blood pressure will be measured on day 14 (at end of each diet phase (fortnightly))

    Measured using digital blood pressure monitor

  7. Mental Health Assessment

    Time frame: Completed at day 1 and end of study (day 56)

    Perceived Stress Scale survey completed by participants

  8. Dietary compliance

    Time frame: Day 1 to Day 14 of specified diet 1 and diet 2 phases

    Measured by participant completed daily diet checklist noting the amount of food they consumed of provided meals during specific diet 1 and 2 phases

  9. Habitual dietary intake

    Time frame: Daily throughout 14-day baseline habitual and habitual washout phases

    Using research food diary mobile phone application

  10. Changes in physical activity levels

    Time frame: Completed at each of each 14-day diet phase

    Using International Physical Activity Questionnaire - Short Form (IPAQ-SF)

  11. Glucose levels

    Time frame: Blood collected at baseline day 1 and day 14 of each phase (fortnightly)

    Blood samples collected will be assessed for glucose levels

  12. Lipid studies

    Time frame: Blood collected at baseline day 1 and day 14 of each phase (fortnightly)

    Blood samples collected will be assessed for lipid studies

  13. Irritable Bowel Syndrome-Severity Scoring System (IBS-SS)

    Time frame: End of each 14-day diet phase

    Completion of Irritable Bowel Syndrome-Severity Scoring System (IBS-SS)

  14. Gastrointestinal symptomatology

    Time frame: Baseline day 1 and day 14 of each diet phase (fortnightly)

    Completion of Gastrointestinal Symptom Rating Scale (GSRS)

  15. Bowel movement

    Time frame: Baseline day 1 and day 14 of each diet phase (fortnightly)

    Completion of Bristol Stool Chart questionnaires

  16. End of study optional semi-structured interview

    Time frame: End of study (at least 8 weeks post-randomisation)

    Interview participants to assess challenges of adhering to study and compliance

Sponsors and collaborators

Lead sponsor

Monash University

Other

Registry information

Official study title

Food Derived Bacteria and Their Role in Treating Disease

Acronym: FIG

Important dates

Study start
2023
Primary completion
2023
Study completion
2023
First posted
Aug 14, 2023
Registry last updated
Apr 24, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Published trials that share one or more normalized conditions with this study.