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Dried Chicory Root in IBD (Chic-IBD)

Primary Purpose

Inflammatory Bowel Diseases, Dietary Exposure

Status
Not yet recruiting
Phase
Not Applicable
Locations
Netherlands
Study Type
Interventional
Intervention
Dried Chicory Root
Sponsored by
University Medical Center Groningen
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional supportive care trial for Inflammatory Bowel Diseases focused on measuring Inflammatory bowel disease, dietary fiber, gut microbiome, inflammation

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria: Men and women aged ≥18 years; Having a diagnosis of IBD (either UC or CD) and undergoing treatment at the policlinic at the University Medical Center Groningen; Mild or moderate IBD, defined as fecal calprotectin levels ≥100 μg and Harvey Bradshaw Index (HBI) <8 for CD patients or Simple Clinical Colitis Activity Index (SCCAI) <5 for UC patients; Using stable maintenance therapy for at least 12 weeks; Being able to read and speak Dutch; Willing to come to the University Medical Center Groningen for practical reasons (visiting the study site); Willing to continue their regular lifestyle patterns during the study. Exclusion Criteria: Having a medical history that may impact study outcomes, such as a diagnosis of diabetes mellitus type 2, heart disease, renal disease, cancer, celiac disease; Having an ileostomy or colostomy, as this greatly impacts bowel function and gut microbiota composition; Having a clinically significant stenosis; Use of antibiotics <4 weeks before study start; Use of prebiotics, probiotics and/or synbiotic (this should be stopped 4 weeks before start of the study) or other fiber supplements such as psyllium; Use of tube feeding or sib-feeding; Being pregnant or lactating; Participation in another clinical study at the same time; Unable or unwilling to comply to study rules

Sites / Locations

  • University Medical Center Groningen

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

Before and after study in 6 patients with UC and 6 patients wiht CD

Arm Description

This is a 4-week before-after pilot study to explore the effectiveness of a WholeFiber Trademark (TM) intervention (a dried vegetable rich in prebiotic intrinsic fibers) on inflammation, fecal gut microbiota and metabolites, IBD-complaints and QoL and assesses its feasibility. In this before-after study, 12 patients with IBD will receive WholeFiberTM; of which 6 patients with CD and 6 patients with UC to assess if there is a difference in effect between these groups of patients.

Outcomes

Primary Outcome Measures

change in fecal calprotectin
To explore the effect of a 4-week 10-20 g/day WholeFiberTM intervention on fecal calprotectin levels in patients with CD and UC.

Secondary Outcome Measures

Change in IBD complaints by HBI for CD
To explore the effect of a 4-week WholeFiberTM intervention on IBD-complaints in patients with CD measured by the Harvey Bradshaw Index (HBI)
Change in IBD complaints by SCCAI for UC
To explore the effect of a 4-week WholeFiberTM intervention on IBD-complaints in patients UC measured by the Simple Clinical Colitis Activity Index (SCCAI)
Change in QOL measured by IBDQ
To explore the effect of a 4-week WholeFiberTM intervention in patients with CD and UC on QoL measured by the IBDQ (Irvine 1999)
Change in the Food-related Quality of Life (FrQOL)
To explore the effect of a 4-week WholeFiberTM intervention in patients with CD and UC on Food-related QoL measured by a validated instrument by Hughes et al 2015
Change in stool consistency
To explore the effect of a 4-week WholeFiberTM intervention in patients with CD and UC on stool consistency. Stool consistency will be measured using the validated Bristol Stool Chart.
Change in stool frequency
To explore the effect of a 4-week WholeFiberTM intervention in patients with CD and UC on stool frequency. Patients will be asked how often they defecated per day during the past week
Change in fecal microbiota composition: Shannon-index
To explore the effect of a 4-week WholeFiberTM intervention in patients with CD and UC on fecal microbiota composition. Next generation sequencing will be used ot determine bacterial richness (Shannon-index)
Change in fecal microbiota composition by beta-diversity
To explore the effect of a 4-week WholeFiberTM intervention in patients with CD and UC on fecal microbiota composition. Next generation sequencing will be used ot determine bacterial interindividual variations (beta-diversity)
Change in fecal SCFA levels: lactate
To explore the effect of a 4-week WholeFiberTM intervention on fecal lactate in patients with CD and UC measured by a conductivity detector.
Change in fecal SCFA levels: formate
To explore the effect of a 4-week WholeFiberTM intervention on fecal formate in patients with CD and UC measured by a conductivity detector.
Change in fecal SCFA levels; butyrate
To explore the effect of a 4-week WholeFiberTM intervention on fecal butyrate in patients with CD and UC measured by a conductivity detector.
Change in fecal SCFA levels: propionate
To explore the effect of a 4-week WholeFiberTM intervention on fecal propionate in patients with CD and UC measured by a conductivity detector.
Change in fecal SCFA levels: acetate
To explore the effect of a 4-week WholeFiberTM intervention on fecal acetate in patients with CD and UC measured by a conductivity detector.
Change in fecal acidity (pH)
To explore the effect of a 4-week WholeFiberTM intervention in patients with CD and UC on fecal acidity (pH) by a PCE-228-R pH and redox meter in a stool sample.
Change in fecal redox status
To explore the effect of a 4-week WholeFiberTM intervention in patients with CD and UC on fecal redox status, measured by PCE-228-R instrument.
Change in serum leukocytes
To explore the effect of a 4-week WholeFiberTM intervention in patients with CD and UC on leukocytes count.
Change in serum thrombocytes
To explore the effect of a 4-week WholeFiberTM intervention in patients with CD and UC on thrombocytes.
Change in serum iron status: serum iron
To explore the effect of a 4-week WholeFiberTM intervention in patients with CD and UC serum iron [micromol/L]
Change in serum iron status: Total Iron Binding Capacity (TIBC)
To explore the effect of a 4-week WholeFiberTM intervention in patients with CD and UC on Total Iron Binding Capacity (TIBC) [micromol/L]
Change in serum iron status: ferritin
To explore the effect of a 4-week WholeFiberTM intervention in patients with CD and UC on ferritin [microg/L]
Change in serum iron status: transferrin
To explore the effect of a 4-week WholeFiberTM intervention in patients with CD and UC on transferrin [g/L]
Change in serum ALAT
To explore the effect of a 4-week WholeFiberTM intervention in patients with CD and UC on Alanine Aminotransferase (ALAT).
Change in serum ASAT
To explore the effect of a 4-week WholeFiberTM intervention in patients with CD and UC on Aspartate Aminotransferase (ALAT).
Change in serum GGT
To explore the effect of a 4-week WholeFiberTM intervention in patients with CD and UC on Gamma-Glutamyl Transferase (GGT)
Change in serum creatinine
To explore the effect of a 4-week WholeFiberTM intervention in patients with CD and UC on iron status.
Change in C-reactive protein (CRP)
To explore the effect of a 4-week WholeFiberTM intervention in patients with CD and UC on C-reactive protein (CRP), which is an inflammation marker.
Change in inflammatory marker IL-6 analysed by an ELISA kit
To explore the effect of a 4-week WholeFiberTM intervention in patients with CD and UC on the inflammatory marker IL-6 on an ELISA kit
Change in inflammatory marker IL-8 analysed by an ELISA kit
To explore the effect of a 4-week WholeFiberTM intervention in patients with CD and UC on the inflammatory marker IL-8 on an ELISA kit
Change in inflammatory marker IL-10 analysed by an ELISA kit
To explore the effect of a 4-week WholeFiberTM intervention in patients with CD and UC on the inflammatory marker IL-10 on an ELISA kit
Change in inflammatory markers IL-12 analysed by an ELISA kit
To explore the effect of a 4-week WholeFiberTM intervention in patients with CD and UC on the inflammatory marker IL-12 on an ELISA kit
Change in inflammatory markerIL-17a analysed by an ELISA kit
To explore the effect of a 4-week WholeFiberTM intervention in patients with CD and UC on the inflammatory marker IL-17a on an ELISA kit
Change in inflammatory marker IL-22 analysed by an ELISA kit
To explore the effect of a 4-week WholeFiberTM intervention in patients with CD and UC on the inflammatory marker IL-22 on an ELISA kit
Change in inflammatory marker IL-23 analysed by an ELISA kit
To explore the effect of a 4-week WholeFiberTM intervention in patients with CD and UC on the inflammatory marker IL-23 on an ELISA kit
Change in inflammatory marker TNF-alpha analysed by an ELISA kit
To explore the effect of a 4-week WholeFiberTM intervention in patients with CD and UC on the inflammatory marker TNF-alpha on an ELISA kit
Change in inflammatory marker Interferon(IFN)-gamma analysed by an ELISA kit
To explore the effect of a 4-week WholeFiberTM intervention in patients with CD and UC on the inflammatory marker Interferon(IFN)-gamma on an ELISA kit
Change in oxidative stress measured by free thiols
To explore the effect of a 4-week WholeFiberTM intervention in patients with CD and UC on oxidative stress measured by free thiols.

Full Information

First Posted
August 8, 2023
Last Updated
September 18, 2023
Sponsor
University Medical Center Groningen
Collaborators
WholeFiber, MyMicroZoo
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1. Study Identification

Unique Protocol Identification Number
NCT06016322
Brief Title
Dried Chicory Root in IBD
Acronym
Chic-IBD
Official Title
The Effect of Dried Chicory Root on Inflammation, Gut Microbiota and Complaints in Patients With Inflammatory Bowel Disease: a Pilot Study
Study Type
Interventional

2. Study Status

Record Verification Date
September 2023
Overall Recruitment Status
Not yet recruiting
Study Start Date
October 2, 2023 (Anticipated)
Primary Completion Date
April 1, 2024 (Anticipated)
Study Completion Date
September 30, 2024 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University Medical Center Groningen
Collaborators
WholeFiber, MyMicroZoo

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
The goal of this clinical pilot trial is to test the use of dried chicory root in patients with IBD. The main questions it aims to answer are: what the effect of a 4-week 10-20 g/day WholeFiberTM intervention on fecal calprotectin, IBD-complaints and QoL, serum inflammatory markers, gut microbiota and SCFA levels in patients with Crohn's disease and ulcerative colitis Participants will receive 1 sachet of 10g WholeFiberTM for the first 2 weeks (equals 8.5 g fiber), and 2 sachets of 10g WholeFiberTM per day for the last two weeks (equals 17 g fiber). Researchers will compare the above mentioned outcomes before and after the intervention.
Detailed Description
Rationale: Inflammatory Bowel Diseases (IBD), of which Ulcerative Colitis (UC) and Crohn's Disease (CD) are the main types, includes recurring episodes of inflammation in the gastro-intestinal tract and severely impacts quality of life (QoL), leads to more hospitalization and increases the mortality risk. An impaired gut microbiota and lower levels of short-chain fatty acids (SCFA) have been linked to the pathophysiology. A higher fiber intake is linked to positive changes in the gut microbiota and increase SCFA-production, however patients with IBD consume too little dietary fiber. WholeFiberTM, a dried vegetable rich in 4 types of prebiotic fiber, may be an easy solution to increase dietary fiber intake, impact the gut microbiota and SCFA, IBD-complaints and health parameters. Objective: To explore the effect of a 4-week 10-20 g/day WholeFiberTM intervention on fecal calprotectin, IBD-complaints and QoL, serum inflammatory markers, gut microbiota and SCFA levels in patients with CD and UC. Study design: this is a 4-week pilot study with one arm to explore the effects of a WholeFiberTM intervention. Measurements will take place before and after the intervention, questionnaires will also be conducted halfway. Study population: in total 12 patients with mild to moderate IBD complaints will be included, of which 6 UC and 6 CD patients, to investigate if there is a difference between the two groups in efficacy of WholeFiberTM. Intervention: Subjects will receive 1 sachet of 10g WholeFiberTM for the first 2 weeks (equals 8.5 g fiber), and 2 sachets of 10g WholeFiberTM per day for the last two weeks (equals 17 g fiber). Main study parameters/endpoints: the primary parameter is change in fecal calprotectin after the 4-week intervention, which is a marker for inflammation in the gut. Secondary parameters are improvements in IBD-complaints, QoL, serum markers, and changes in the gut microbiota and increase in fecal SCFA-production. Moreover, it will be explored whether the response on the intervention will be different between UC and CD. Furthermore, an evaluation questionnaire will be conducted to assess feasibility and acceptance of the WholeFiberTM intervention in this population.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Inflammatory Bowel Diseases, Dietary Exposure
Keywords
Inflammatory bowel disease, dietary fiber, gut microbiome, inflammation

7. Study Design

Primary Purpose
Supportive Care
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Model Description
Pilot study investigating the effect of additional dietary intake 10-20 gram of a dried vegetable fibre. The difference in outcomes before and after the intervention in fecal calprotectin, IBD complaints, QOL, serum inflammatory markers, gut microbiota and SCFA will be determined
Masking
None (Open Label)
Allocation
N/A
Enrollment
12 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Before and after study in 6 patients with UC and 6 patients wiht CD
Arm Type
Experimental
Arm Description
This is a 4-week before-after pilot study to explore the effectiveness of a WholeFiber Trademark (TM) intervention (a dried vegetable rich in prebiotic intrinsic fibers) on inflammation, fecal gut microbiota and metabolites, IBD-complaints and QoL and assesses its feasibility. In this before-after study, 12 patients with IBD will receive WholeFiberTM; of which 6 patients with CD and 6 patients with UC to assess if there is a difference in effect between these groups of patients.
Intervention Type
Dietary Supplement
Intervention Name(s)
Dried Chicory Root
Other Intervention Name(s)
WholeFiber Trademark (TM)
Intervention Description
Subjects will receive 1 sachet of 10g WholeFiberTM for the first 2 weeks (equals 8.5 g fiber), and 2 sachets of 10g WholeFiberTM per day for the last two weeks (equals 17 g fiber). WholeFiberTM is a fiber-rich dried vegetable made from the chicory root that contains four types of prebiotic fibers (inulin, pectin, cellulose, hemi-cellulose).
Primary Outcome Measure Information:
Title
change in fecal calprotectin
Description
To explore the effect of a 4-week 10-20 g/day WholeFiberTM intervention on fecal calprotectin levels in patients with CD and UC.
Time Frame
difference between baseline and after 4-week intervention
Secondary Outcome Measure Information:
Title
Change in IBD complaints by HBI for CD
Description
To explore the effect of a 4-week WholeFiberTM intervention on IBD-complaints in patients with CD measured by the Harvey Bradshaw Index (HBI)
Time Frame
difference between baseline and after 4-week intervention
Title
Change in IBD complaints by SCCAI for UC
Description
To explore the effect of a 4-week WholeFiberTM intervention on IBD-complaints in patients UC measured by the Simple Clinical Colitis Activity Index (SCCAI)
Time Frame
difference between baseline and after 4-week intervention
Title
Change in QOL measured by IBDQ
Description
To explore the effect of a 4-week WholeFiberTM intervention in patients with CD and UC on QoL measured by the IBDQ (Irvine 1999)
Time Frame
difference between baseline and after 4-week intervention
Title
Change in the Food-related Quality of Life (FrQOL)
Description
To explore the effect of a 4-week WholeFiberTM intervention in patients with CD and UC on Food-related QoL measured by a validated instrument by Hughes et al 2015
Time Frame
difference between baseline and after 4-week intervention
Title
Change in stool consistency
Description
To explore the effect of a 4-week WholeFiberTM intervention in patients with CD and UC on stool consistency. Stool consistency will be measured using the validated Bristol Stool Chart.
Time Frame
difference between baseline and after 4-week intervention
Title
Change in stool frequency
Description
To explore the effect of a 4-week WholeFiberTM intervention in patients with CD and UC on stool frequency. Patients will be asked how often they defecated per day during the past week
Time Frame
difference between baseline and after 4-week intervention
Title
Change in fecal microbiota composition: Shannon-index
Description
To explore the effect of a 4-week WholeFiberTM intervention in patients with CD and UC on fecal microbiota composition. Next generation sequencing will be used ot determine bacterial richness (Shannon-index)
Time Frame
difference between baseline and after 4-week intervention
Title
Change in fecal microbiota composition by beta-diversity
Description
To explore the effect of a 4-week WholeFiberTM intervention in patients with CD and UC on fecal microbiota composition. Next generation sequencing will be used ot determine bacterial interindividual variations (beta-diversity)
Time Frame
difference between baseline and after 4-week intervention
Title
Change in fecal SCFA levels: lactate
Description
To explore the effect of a 4-week WholeFiberTM intervention on fecal lactate in patients with CD and UC measured by a conductivity detector.
Time Frame
difference between baseline and after 4-week intervention
Title
Change in fecal SCFA levels: formate
Description
To explore the effect of a 4-week WholeFiberTM intervention on fecal formate in patients with CD and UC measured by a conductivity detector.
Time Frame
difference between baseline and after 4-week intervention
Title
Change in fecal SCFA levels; butyrate
Description
To explore the effect of a 4-week WholeFiberTM intervention on fecal butyrate in patients with CD and UC measured by a conductivity detector.
Time Frame
difference between baseline and after 4-week intervention
Title
Change in fecal SCFA levels: propionate
Description
To explore the effect of a 4-week WholeFiberTM intervention on fecal propionate in patients with CD and UC measured by a conductivity detector.
Time Frame
difference between baseline and after 4-week intervention
Title
Change in fecal SCFA levels: acetate
Description
To explore the effect of a 4-week WholeFiberTM intervention on fecal acetate in patients with CD and UC measured by a conductivity detector.
Time Frame
difference between baseline and after 4-week intervention
Title
Change in fecal acidity (pH)
Description
To explore the effect of a 4-week WholeFiberTM intervention in patients with CD and UC on fecal acidity (pH) by a PCE-228-R pH and redox meter in a stool sample.
Time Frame
difference between baseline and after 4-week intervention
Title
Change in fecal redox status
Description
To explore the effect of a 4-week WholeFiberTM intervention in patients with CD and UC on fecal redox status, measured by PCE-228-R instrument.
Time Frame
difference between baseline and after 4-week intervention
Title
Change in serum leukocytes
Description
To explore the effect of a 4-week WholeFiberTM intervention in patients with CD and UC on leukocytes count.
Time Frame
difference between baseline and after 4-week intervention
Title
Change in serum thrombocytes
Description
To explore the effect of a 4-week WholeFiberTM intervention in patients with CD and UC on thrombocytes.
Time Frame
difference between baseline and after 4-week intervention
Title
Change in serum iron status: serum iron
Description
To explore the effect of a 4-week WholeFiberTM intervention in patients with CD and UC serum iron [micromol/L]
Time Frame
difference between baseline and after 4-week intervention
Title
Change in serum iron status: Total Iron Binding Capacity (TIBC)
Description
To explore the effect of a 4-week WholeFiberTM intervention in patients with CD and UC on Total Iron Binding Capacity (TIBC) [micromol/L]
Time Frame
difference between baseline and after 4-week intervention
Title
Change in serum iron status: ferritin
Description
To explore the effect of a 4-week WholeFiberTM intervention in patients with CD and UC on ferritin [microg/L]
Time Frame
difference between baseline and after 4-week intervention
Title
Change in serum iron status: transferrin
Description
To explore the effect of a 4-week WholeFiberTM intervention in patients with CD and UC on transferrin [g/L]
Time Frame
difference between baseline and after 4-week intervention
Title
Change in serum ALAT
Description
To explore the effect of a 4-week WholeFiberTM intervention in patients with CD and UC on Alanine Aminotransferase (ALAT).
Time Frame
difference between baseline and after 4-week intervention
Title
Change in serum ASAT
Description
To explore the effect of a 4-week WholeFiberTM intervention in patients with CD and UC on Aspartate Aminotransferase (ALAT).
Time Frame
difference between baseline and after 4-week intervention
Title
Change in serum GGT
Description
To explore the effect of a 4-week WholeFiberTM intervention in patients with CD and UC on Gamma-Glutamyl Transferase (GGT)
Time Frame
difference between baseline and after 4-week intervention
Title
Change in serum creatinine
Description
To explore the effect of a 4-week WholeFiberTM intervention in patients with CD and UC on iron status.
Time Frame
difference between baseline and after 4-week intervention
Title
Change in C-reactive protein (CRP)
Description
To explore the effect of a 4-week WholeFiberTM intervention in patients with CD and UC on C-reactive protein (CRP), which is an inflammation marker.
Time Frame
difference between baseline and after 4-week intervention
Title
Change in inflammatory marker IL-6 analysed by an ELISA kit
Description
To explore the effect of a 4-week WholeFiberTM intervention in patients with CD and UC on the inflammatory marker IL-6 on an ELISA kit
Time Frame
difference between baseline and after 4-week intervention
Title
Change in inflammatory marker IL-8 analysed by an ELISA kit
Description
To explore the effect of a 4-week WholeFiberTM intervention in patients with CD and UC on the inflammatory marker IL-8 on an ELISA kit
Time Frame
difference between baseline and after 4-week intervention
Title
Change in inflammatory marker IL-10 analysed by an ELISA kit
Description
To explore the effect of a 4-week WholeFiberTM intervention in patients with CD and UC on the inflammatory marker IL-10 on an ELISA kit
Time Frame
difference between baseline and after 4-week intervention
Title
Change in inflammatory markers IL-12 analysed by an ELISA kit
Description
To explore the effect of a 4-week WholeFiberTM intervention in patients with CD and UC on the inflammatory marker IL-12 on an ELISA kit
Time Frame
difference between baseline and after 4-week intervention
Title
Change in inflammatory markerIL-17a analysed by an ELISA kit
Description
To explore the effect of a 4-week WholeFiberTM intervention in patients with CD and UC on the inflammatory marker IL-17a on an ELISA kit
Time Frame
difference between baseline and after 4-week intervention
Title
Change in inflammatory marker IL-22 analysed by an ELISA kit
Description
To explore the effect of a 4-week WholeFiberTM intervention in patients with CD and UC on the inflammatory marker IL-22 on an ELISA kit
Time Frame
difference between baseline and after 4-week intervention
Title
Change in inflammatory marker IL-23 analysed by an ELISA kit
Description
To explore the effect of a 4-week WholeFiberTM intervention in patients with CD and UC on the inflammatory marker IL-23 on an ELISA kit
Time Frame
difference between baseline and after 4-week intervention
Title
Change in inflammatory marker TNF-alpha analysed by an ELISA kit
Description
To explore the effect of a 4-week WholeFiberTM intervention in patients with CD and UC on the inflammatory marker TNF-alpha on an ELISA kit
Time Frame
difference between baseline and after 4-week intervention
Title
Change in inflammatory marker Interferon(IFN)-gamma analysed by an ELISA kit
Description
To explore the effect of a 4-week WholeFiberTM intervention in patients with CD and UC on the inflammatory marker Interferon(IFN)-gamma on an ELISA kit
Time Frame
difference between baseline and after 4-week intervention
Title
Change in oxidative stress measured by free thiols
Description
To explore the effect of a 4-week WholeFiberTM intervention in patients with CD and UC on oxidative stress measured by free thiols.
Time Frame
difference between baseline and after 4-week intervention
Other Pre-specified Outcome Measures:
Title
Difference in change in fecal calprotectin between patients with CD and UC
Description
To explore the difference between CD an UC in change in the effect of a 4-week 10-20 g/day WholeFiberTM intervention on fecal calprotectin levels
Time Frame
difference between baseline and after 4-week intervention
Title
Appreciation of WholeFiberTM evaluated by patients with CD and UC?
Description
How participants with CD and UC appreciated of WholeFiberTM by chosing a digit on a vascale from 1 to 10, being 1 the lowest number of appreciation and 10 the highest number
Time Frame
after 4-week intervention
Title
The convenience of the use of WholeFiberTM evaluated by patients with CD and UC?
Description
Participants are asked to rate the following statement "I find Whole Fiber easy to use" and can answer on a Lickert with 5 different categories: 1. completely disagree 2. disagree 3. neutral, 4 agree 5. completely agree.
Time Frame
after 4-week intervention
Title
The palatability of the use of WholeFiberTM evaluated by patients with CD and UC?
Description
Participants are asked to rate the following statement "I find Whole Fiber tasty to eat" and can answer on a Lickert with 5 different categories: 1. completely disagree 2. disagree 3. neutral, 4 agree 5. completely agree.
Time Frame
after 4-week intervention

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Men and women aged ≥18 years; Having a diagnosis of IBD (either UC or CD) and undergoing treatment at the policlinic at the University Medical Center Groningen; Mild or moderate IBD, defined as fecal calprotectin levels ≥100 μg and Harvey Bradshaw Index (HBI) <8 for CD patients or Simple Clinical Colitis Activity Index (SCCAI) <5 for UC patients; Using stable maintenance therapy for at least 12 weeks; Being able to read and speak Dutch; Willing to come to the University Medical Center Groningen for practical reasons (visiting the study site); Willing to continue their regular lifestyle patterns during the study. Exclusion Criteria: Having a medical history that may impact study outcomes, such as a diagnosis of diabetes mellitus type 2, heart disease, renal disease, cancer, celiac disease; Having an ileostomy or colostomy, as this greatly impacts bowel function and gut microbiota composition; Having a clinically significant stenosis; Use of antibiotics <4 weeks before study start; Use of prebiotics, probiotics and/or synbiotic (this should be stopped 4 weeks before start of the study) or other fiber supplements such as psyllium; Use of tube feeding or sib-feeding; Being pregnant or lactating; Participation in another clinical study at the same time; Unable or unwilling to comply to study rules
Facility Information:
Facility Name
University Medical Center Groningen
City
Groningen
ZIP/Postal Code
9713GZ
Country
Netherlands

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
32199025
Citation
Puhlmann ML, de Vos WM. Back to the Roots: Revisiting the Use of the Fiber-Rich Cichorium intybusL. Taproots. Adv Nutr. 2020 Jul 1;11(4):878-889. doi: 10.1093/advances/nmaa025. Erratum In: Adv Nutr. 2021 Jul 30;12(4):1598.
Results Reference
result
PubMed Identifier
34486663
Citation
Peters V, Dijkstra G, Campmans-Kuijpers MJE. Are all dietary fibers equal for patients with inflammatory bowel disease? A systematic review of randomized controlled trials. Nutr Rev. 2022 Apr 8;80(5):1179-1193. doi: 10.1093/nutrit/nuab062.
Results Reference
result
PubMed Identifier
36059540
Citation
Puhlmann ML, de Vos WM. Intrinsic dietary fibers and the gut microbiome: Rediscovering the benefits of the plant cell matrix for human health. Front Immunol. 2022 Aug 18;13:954845. doi: 10.3389/fimmu.2022.954845. eCollection 2022.
Results Reference
result
Links:
URL
https://www.cambridge.org/core/journals/gut-microbiome/article/dried-chicory-root-improves-bowel-function-benefits-intestinal-microbial-trophic-chains-and-increases-faecal-and-circulating-short-chain-fatty-acids-in-subjects-at-risk-for-type-2-diabetes/6209AEAFBDDB181197F22AE24388186B
Description
Dried Chicory Root Improves Bowel Function, Benefits Intestinal Microbial Trophic Chains and Increases Faecal and Circulating Short Chain Fatty Acids in Subjects at Risk for Type 2 Diabetes

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Dried Chicory Root in IBD

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