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Bread Study: Comparison of the Tolerance of Spelt and Wheat Bread

Primary Purpose

Non-celiac Gluten Sensitivity, Wheat Intolerance

Status
Completed
Phase
Not Applicable
Locations
Germany
Study Type
Interventional
Intervention
bread
Sponsored by
University of Hohenheim
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional supportive care trial for Non-celiac Gluten Sensitivity focused on measuring Human Nutrition, NCWS, Spelt, Wheat Bread

Eligibility Criteria

18 Years - 70 Years (Adult, Older Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

  • Age ≥18 ≤70 years
  • Signed declaration of consent
  • Willingness to adhere to the prescribed diet for the duration of the study
  • Subjective bread wheat intolerance
  • No known spelled intolerance
  • No acute or chronic gastrointestinal diseases (e.g. celiac disease / wheat allergy)
  • No participation in another clinical trial (current or within the past 30 days)
  • Gluten-containing diet at least 6 weeks before the start of the study

Exclusion Criteria:

  • Taking intestinal therapeutics, antibiotics, immunosuppressants or similar
  • Pregnancy / lactation
  • Relevant violations of the nutritional protocol
  • Occurrence of relevant diseases (possibly individual decision)
  • Revocation of consent
  • Accommodation in a clinic or similar facility based on an official or judicial order

Sites / Locations

  • University of Hohenheim

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm 4

Arm 5

Arm 6

Arm Type

Active Comparator

Active Comparator

Experimental

Experimental

Experimental

Experimental

Arm Label

Gluten free bread with added gluten

Gluten free bread with added FODMAPs

Traditional manufactured wheat bread

Traditional manufactured spelt bread

Conventional manufactured wheat bread

Conventional manufactured spelt bread

Arm Description

Bread will be eaten by the participants for 4 consecutive days.

Bread will be eaten by the participants for 4 consecutive days.

Bread will be eaten by the participants for 4 consecutive days.

Bread will be eaten by the participants for 4 consecutive days.

Bread will be eaten by the participants for 4 consecutive days.

Bread will be eaten by the participants for 4 consecutive days.

Outcomes

Primary Outcome Measures

Change of IBS-SSS Total score
IBS-SSS Total score will be collected with a questionnaire

Secondary Outcome Measures

Extraintestinal Symptoms
The study team will ask the participants for typical extraintestinal symptoms in NCWS like headache, foggy-mind, nausea, heartburn, exhaustion
Blood and fecal markers
Change of blood- and fecal markers that will reveal inflammation or intestinal permeability (Anti-gliadin Immunglobulin G antibody, lipase, ferritin, zonulin, calprotectin and lactoferrin)

Full Information

First Posted
May 14, 2020
Last Updated
October 26, 2021
Sponsor
University of Hohenheim
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1. Study Identification

Unique Protocol Identification Number
NCT04401956
Brief Title
Bread Study: Comparison of the Tolerance of Spelt and Wheat Bread
Official Title
Comparison of the Tolerance of Spelt and Wheat Bread in Humans With Suspected NCWS Considering Different Manufacturing Processes of Bread
Study Type
Interventional

2. Study Status

Record Verification Date
October 2021
Overall Recruitment Status
Completed
Study Start Date
May 15, 2020 (Actual)
Primary Completion Date
August 10, 2021 (Actual)
Study Completion Date
September 7, 2021 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of Hohenheim

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No

5. Study Description

Brief Summary
This project aims to verify the hypothesis that spelt products are more tolerable than bread wheat products in a target group of individuals with self-diagnosed wheat sensitivity. In addition, the influence of different manufacturing processes will be considered.
Detailed Description
Wheat cereals are known to be capable of triggering wheat allergy and celiac disease. The prevalence of both diseases is about 1%. Recently, another clinical entity was described, the non-celiac wheat sensitivity (NCWS). The origin and mechanisms of NCWS are unclear at present, but the existence of this new disease entity has been proven by double-blind placebo-controlled challenge tests. Three different grain components have been proposed as triggers of NCWS, gluten, α-amylase trypsin inhibitors or fermentable carbohydrates (FODMAPs). It is reported that individuals with self-diagnosed NCWS quite often tolerate spelt products much better, even though spelt shows a higher gluten content than bread wheat products. Therefore, the question arises whether this putative spelt tolerance can be confirmed on an objective basis and whether the underlying molecular mechanisms can be elucidated. So far, human study addressing such questions are lacking. This project aims to verify the hypothesis that spelt products are more tolerable than bread wheat products in a target group of individuals with self-diagnosed wheat sensitivity. In addition, the influence of different manufacturing processes on wheat sensitivity will be revealed. For this purpose, the trial involves individuals with self-diagnosed wheat sensitivity and spelt tolerance. Six different kinds of bread will be tested, including 4 wheat and spelt breads, each of them produced following a traditional or a conventional way. Aim of this part is to objective bread wheat and spelt intolerance in a defined population. To find out whether FODMAPs or gluten affect the tolerance of bread, two additional breads will be tested, a gluten-free bread with added gluten and a gluten-free bread with added FODMAPs.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Non-celiac Gluten Sensitivity, Wheat Intolerance
Keywords
Human Nutrition, NCWS, Spelt, Wheat Bread

7. Study Design

Primary Purpose
Supportive Care
Study Phase
Not Applicable
Interventional Study Model
Crossover Assignment
Masking
Participant
Allocation
Randomized
Enrollment
24 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Gluten free bread with added gluten
Arm Type
Active Comparator
Arm Description
Bread will be eaten by the participants for 4 consecutive days.
Arm Title
Gluten free bread with added FODMAPs
Arm Type
Active Comparator
Arm Description
Bread will be eaten by the participants for 4 consecutive days.
Arm Title
Traditional manufactured wheat bread
Arm Type
Experimental
Arm Description
Bread will be eaten by the participants for 4 consecutive days.
Arm Title
Traditional manufactured spelt bread
Arm Type
Experimental
Arm Description
Bread will be eaten by the participants for 4 consecutive days.
Arm Title
Conventional manufactured wheat bread
Arm Type
Experimental
Arm Description
Bread will be eaten by the participants for 4 consecutive days.
Arm Title
Conventional manufactured spelt bread
Arm Type
Experimental
Arm Description
Bread will be eaten by the participants for 4 consecutive days.
Intervention Type
Other
Intervention Name(s)
bread
Intervention Description
Different types of bread
Primary Outcome Measure Information:
Title
Change of IBS-SSS Total score
Description
IBS-SSS Total score will be collected with a questionnaire
Time Frame
Study examinations are at baseline, after wash out phases (day 3, 10, 17, 24, 31, 38) and after bread intervention phases (day 7, 14, 21, 28, 35, 42).)
Secondary Outcome Measure Information:
Title
Extraintestinal Symptoms
Description
The study team will ask the participants for typical extraintestinal symptoms in NCWS like headache, foggy-mind, nausea, heartburn, exhaustion
Time Frame
Study examinations are at baseline, after wash out phases (day 3, 10, 17, 24, 31, 38) and after bread intervention phases (day 7, 14, 21, 28, 35, 42).)
Title
Blood and fecal markers
Description
Change of blood- and fecal markers that will reveal inflammation or intestinal permeability (Anti-gliadin Immunglobulin G antibody, lipase, ferritin, zonulin, calprotectin and lactoferrin)
Time Frame
Study examinations are at baseline and after bread intervention phases (day 7, 14, 21, 28, 35, 42).

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
70 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Age ≥18 ≤70 years Signed declaration of consent Willingness to adhere to the prescribed diet for the duration of the study Subjective bread wheat intolerance No known spelled intolerance No acute or chronic gastrointestinal diseases (e.g. celiac disease / wheat allergy) No participation in another clinical trial (current or within the past 30 days) Gluten-containing diet at least 6 weeks before the start of the study Exclusion Criteria: Taking intestinal therapeutics, antibiotics, immunosuppressants or similar Pregnancy / lactation Relevant violations of the nutritional protocol Occurrence of relevant diseases (possibly individual decision) Revocation of consent Accommodation in a clinic or similar facility based on an official or judicial order
Facility Information:
Facility Name
University of Hohenheim
City
Stuttgart
ZIP/Postal Code
70599
Country
Germany

12. IPD Sharing Statement

Plan to Share IPD
Undecided

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Bread Study: Comparison of the Tolerance of Spelt and Wheat Bread

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