NCT02177279

Brief Summary

There is a lot of evidence to suggest that eating a diet rich in cereals such as wheat bran are beneficial in protecting us from diseases such as heart disease, diabetes and cancer. It is still not clear exactly why this happens, but it is likely that the compounds which enter our bodies when we eat such products are responsible. In this study we plan to find out what these compounds are and where they are found. The investigators will do this by asking volunteers to eat a wheat-bran meal and then measuring the compounds that appear in blood, urine and stool samples over the next twenty-four hours. Once the investigators know how much and which compounds are present, we can then find out possible reasons why they are protective, for example by looking to see whether they are anti-inflammatory. We also plan to look at whether if having a diet which contains either a lot of wheat-bran products or very low amounts of these foods effects how they are absorbed by the body. HYPOTHESIS: Wheat bran from ready-to-eat cereal has unique phytochemical profiles which are metabolized to compounds responsible for high cellular bioactivity imparting important health benefits.

Trial Health

80
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
8

participants targeted

Target at below P25 for not_applicable

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

December 1, 2011

Completed
1.2 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

February 1, 2013

Completed
1.4 years until next milestone

First Submitted

Initial submission to the registry

June 19, 2014

Completed
8 days until next milestone

First Posted

Study publicly available on registry

June 27, 2014

Completed
Last Updated

July 8, 2014

Status Verified

July 1, 2014

Enrollment Period

1.2 years

First QC Date

June 19, 2014

Last Update Submit

July 7, 2014

Conditions

Keywords

Wheat bran cereals, bran phytochemicals, phytochemicals bioavailability

Outcome Measures

Primary Outcomes (9)

  • Human bioavailability of benzoic acids and derivatives from wheat bran cereals

    The analysis of the benzoic acid and derivatives metabolites in blood, urine, faecal samples after consumption of 40g and 120g wheat bran cereals, over 24 h period (change from baseline time 0h).

    over 24 h

  • Human bioavailability of cinnamic acids and derivatives from wheat bran cereals

    The analysis of the cinnamic acids and derivatives metabolites in blood, urine, faecal samples after consumption of 40g and 120g wheat bran cereals, over 24 h period (change from baseline time 0h).

    over 24h

  • Human bioavailability of phenylpropanoid dimers from wheat bran cereals

    The analysis of the phenylpropanoid dimers metabolites in blood, urine, faecal samples after consumption of 40g and 120g wheat bran cereals, over 24 h period (change from baseline time 0h).

    over 24h

  • Human bioavailability of phenyl propionic acids from wheat bran cereals

    The analysis of the phenyl propionic acids metabolites in blood, urine, faecal samples after consumption of 40g and 120g wheat bran cereals, over 24 h period (change from baseline time 0h).

    over 24h

  • Bioavailability of benzaldehydes from wheat bran

    The analysis of the benzaldehydes metabolites in blood, urine, faecal samples after consumption of 40g and 120g wheat bran cereals, over 24 h period (change from baseline time 0h).

    over 24h

  • Human bioavailability of acetophenones from wheat bran cereals

    The analysis of the acetophenones metabolites in blood, urine, faecal samples after consumption of 40g and 120g wheat bran cereals, over 24 h period (change from baseline time 0h).

    over 24h

  • Human bioavailability of lignans from wheat bran cereals

    The analysis of the lignans metabolites in blood, urine, faecal samples after consumption of 40g and 120g wheat bran cereals, over 24 h period (change from baseline time 0h).

    over 24 h

  • Short chain fatty acids profile after wheat bran consumption (acute)

    Short chain fatty acids profile in faecal samples at 0h (baseline) and 24h after wheat bran consumption (40g and 120g).

    24 h

  • Short chain fatty acids profile after wheat bran consumption (chronic)

    Short chain fatty acids profile in in faecal samples at day 0 (baseline), day 5 (during 7 days consumption of 40g wheat bran cereals/day) and day 10 (after 120g wheat bran cereals consumption on day 9).

    9 days

Study Arms (3)

Visit A- 120g wheat bran cereals

OTHER

A morning vist where volunteers consumed 120g of wheat bran cereals with 125ml semi-skimmed milk

Other: Visit A high wheat bran

Visit B-40g wheat bran cereals

OTHER

A morning vist where volunteers consumed 40g of wheat bran cereals with 375 ml semi-skimmed milk

Other: Visit B normal wheat bran

Follow up-40g (8days), 120g (1day) wheat bran cereals

OTHER

Volunteers follow their normal diet but they were asked to consume 40g wheat bran cereals with 125 ml semi-skimmed milk for eight days and on day nine 120g wheat bran cereals with 375ml semi-skimmed milk

Other: Follow up normal (8days) and high (1day) bran consumption

Interventions

Visit A- 120g wheat bran cereals
Visit B-40g wheat bran cereals
Follow up-40g (8days), 120g (1day) wheat bran cereals

Eligibility Criteria

Age18 Years - 55 Years
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64)

You may qualify if:

  • Volunteers will be healthy males or females and aged between 18 and 55 years who have a documented low (less than 1 portion per week) or high (more than or equal 5 portions per week) consumption of wheat bran and are able to give informed consent.

You may not qualify if:

  • are taking any medicines prescribed by their general practitioner
  • are taking drugs to lower high cholesterol levels or high blood pressure
  • regularly take analgesics, antipyretic or anti-inflammatories
  • regularly take nutritional supplements
  • have taken antibiotics in the last three months
  • have given a large blood donation in last three months

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Rowett Institute of Nutrition and Health, University of Aberdeen

Aberdeen, Aberdeenshire, AB21 9SB, United Kingdom

Location

Study Officials

  • Wendy R Russell, PhD

    Rowett Institute of Nutrition and Health, University of Aberdeen

    PRINCIPAL INVESTIGATOR
  • Baukje de Roos, PhD

    Rowett Institute of Nutrition and Health, University of Aberdeen

    PRINCIPAL INVESTIGATOR
  • Garry Duthie, Professor

    Rowett Institute of Nutrition and Health, University of Aberdeen

    PRINCIPAL INVESTIGATOR
  • Jolene McMonagle, PhD

    Kellogg Company

    PRINCIPAL INVESTIGATOR
  • Reg Fletcher, PhD

    Kellogg Company

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
interventional
Phase
not applicable
Allocation
NON RANDOMIZED
Masking
NONE
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

June 19, 2014

First Posted

June 27, 2014

Study Start

December 1, 2011

Primary Completion

February 1, 2013

Last Updated

July 8, 2014

Record last verified: 2014-07

Locations