BASE Facility
Notting Hill, Victoria, 3168, Australia
NCT Number: NCT05986955
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.
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Notify Me18 year–65 year
All sexes
Interventional
Early Phase 1
Notting Hill, Victoria, 3168, Australia
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.
Healthy volunteers accepted: Yes
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
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.
Time frame: Day 1, 4, 7, 11 and 14 of each phase
Sequencing and bacterial culturing of stool samples
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
Time frame: Height will be measured on day 14 (at end of each diet phase (fortnightly))
Measured by stadiometer
Time frame: Weight will be measured on day 14 (at end of each diet phase (fortnightly))
Measured using balance scales
Time frame: Baseline day 1 and end of each 14-day diet phase
Measured using standard measuring tape
Time frame: Baseline day 1 and end of each 14-day diet phase
Measured using standard measuring tape
Time frame: Blood pressure will be measured on day 14 (at end of each diet phase (fortnightly))
Measured using digital blood pressure monitor
Time frame: Completed at day 1 and end of study (day 56)
Perceived Stress Scale survey completed by participants
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
Time frame: Daily throughout 14-day baseline habitual and habitual washout phases
Using research food diary mobile phone application
Time frame: Completed at each of each 14-day diet phase
Using International Physical Activity Questionnaire - Short Form (IPAQ-SF)
Time frame: Blood collected at baseline day 1 and day 14 of each phase (fortnightly)
Blood samples collected will be assessed for glucose levels
Time frame: Blood collected at baseline day 1 and day 14 of each phase (fortnightly)
Blood samples collected will be assessed for lipid studies
Time frame: End of each 14-day diet phase
Completion of Irritable Bowel Syndrome-Severity Scoring System (IBS-SS)
Time frame: Baseline day 1 and day 14 of each diet phase (fortnightly)
Completion of Gastrointestinal Symptom Rating Scale (GSRS)
Time frame: Baseline day 1 and day 14 of each diet phase (fortnightly)
Completion of Bristol Stool Chart questionnaires
Time frame: End of study (at least 8 weeks post-randomisation)
Interview participants to assess challenges of adhering to study and compliance
Monash University
Other
Food Derived Bacteria and Their Role in Treating Disease
Acronym: FIG
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.
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