ClinicalTrials.Veeva

Menu

Polyphenols, Prebiotics, the Gut Microbiome and Stress

University of Reading logo

University of Reading

Status

Completed

Conditions

Gut Bacteria
Stress, Psychological

Treatments

Dietary Supplement: prebiotics and polyphenols
Dietary Supplement: GOS, Inulin, RS2
Dietary Supplement: Blueberry, cranberry, green tea extract, cocoa
Dietary Supplement: Maltodextrin

Study type

Interventional

Funder types

Other
Other U.S. Federal agency

Identifiers

Details and patient eligibility

About

The aim of this study is to evaluate how different combinations of prebiotics and polyphenols affect the gut microbiota and perceived cognitive state. 40 volunteers will take part in this study who will be randomised into 4 different groups. One group will consume a placebo, whereas the other groups will consume prebiotics, polyphenols, or a combination of the two.

Full description

  • All participants will be asked to fill out a health screening questionnaire and inclusion/exclusion criteria will be reviewed for volunteer eligibility
  • Valid informed consent will be obtained from the volunteer.
  • Once the study begins, participants will be randomly allocated into 1 of 4 groups each assigned a different polyphenol or prebiotic product. the prebiotic content is dosed as follows: Inulin at 5g/d, GOS at 5g/d and Resistant Starch at 20g/d.
  • Participants will be asked to consume their assigned product once per day. The length of the intervention is 14 days
  • Participants will provide two stool samples: one on day 0 and one on day 14 of the study to identify changes in gut microbiota composition
  • Urine samples will also be provided at day 0 and at day 14 looking for changes in urinary metabolites
  • Participants will also be asked to fill out various mood related questionnaires on days 0 and 14 of the study.
  • You will take your own blood pressure and heart rate on day 0 and day 14 and at least 3 times per week to try and link changes in gut microbiota composition with vascular health.
  • Volunteers will be given containers and specimen pots to take home for initial and final faecal and urine collections. No treatment will be issued until initial stool and urine sample has been provided
  • Maintenance of normal dietary patterns throughout the study is essential and participants will be required to complete food and drink logs throughout the study via a web-based app - on three consecutive days with one of the days being a weekend

Enrollment

20 patients

Sex

All

Ages

18 to 65 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Volunteer is healthy at the time of pre-examination
  • Volunteer has high perceived stress levels (own self-assessment)
  • Volunteer is aged ≥ 18 to ≤ 65 years at the time of pre-examination
  • Volunteer is able and willing to comply with the study instructions
  • Volunteer is suitable for participation in the study according to the investigator/study personnel
  • Written informed consent is given by volunteer

Exclusion criteria

  • No command of any local language
  • Gastrointestinal disorders including IBS, IBD or other conditions that might affect the gut environment
  • Food allergies or intolerances
  • Using drugs (e.g. antibiotics) influencing gastrointestinal function (8 weeks before intervention)
  • Use of laxatives
  • Participants with any form of diagnosed diabetes (types I and II)
  • Volunteers currently involved or will be involved in another clinical or food study
  • History of drug (pharmaceutical or recreational) or alcohol abuse.
  • participants are pregnant or are lactating
  • Regular intake of probiotic or prebiotic supplements
  • Smoking

Trial design

Primary purpose

Prevention

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

20 participants in 4 patient groups, including a placebo group

Polyphenol
Experimental group
Description:
Consume polyphenol combination for two weeks
Treatment:
Dietary Supplement: Blueberry, cranberry, green tea extract, cocoa
Prebiotic
Experimental group
Description:
Consume prebiotic combination for two weeks
Treatment:
Dietary Supplement: GOS, Inulin, RS2
prebiotic and polyphenol
Experimental group
Description:
Combination of prebiotics and polyphenols for two weeks
Treatment:
Dietary Supplement: prebiotics and polyphenols
Placebo
Placebo Comparator group
Description:
maltodextrin placebo for two weeks
Treatment:
Dietary Supplement: Maltodextrin

Trial contacts and locations

1

Loading...

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2026 Veeva Systems