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Designing a Personalized Diet to Reduce the Risk of Crohn's Disease Onset

Primary Purpose

Diet, Healthy, High Risk

Status
Not yet recruiting
Phase
Not Applicable
Locations
Study Type
Interventional
Intervention
Mediteranean to Western to Mediteranean Diet
Western to Mediteranean to Western Diet
Sponsored by
Mount Sinai Hospital, Canada
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Diet, Healthy

Eligibility Criteria

18 Years - 35 Years (Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

  • Healthy, asymptomatic first degree relative (child or sibling) of someone with Crohn's disease
  • Have at least 1 bowel movement every other day

Exclusion Criteria:

  • Received antibiotic treatment within 3 months of recruitment
  • Unintentional weight loss in the last 3 months more than 15% of baseline weight
  • Have ever been diagnosed with any chronic or recurring gastro-intestinal disease or bowel disease
  • Belly pain occurred more than once per week for longer than three months in the past year
  • Diarrhea (>three times per day) has been occurring for more than three months in the last year
  • Have blood in their stool with most stools
  • Diagnosed with diabetes
  • Diagnosed with Celiac disease
  • Diagnosed with irritable bowel syndrome
  • Diagnosed with inflammatory bowel disease
  • Presents significant symptoms of gastrointestinal disease
  • Pregnant or breastfeeding women
  • Has any serious food allergies
  • Diagnosed with lactose intolerance
  • Unable to stop NSAID or probiotic use during the study

Sites / Locations

    Arms of the Study

    Arm 1

    Arm 2

    Arm Type

    Other

    Other

    Arm Label

    Western to Mediteranean to Western Diet

    Mediteranean to Western to Mediteranean Diet

    Arm Description

    Weeks 2 and 3 = WD Weeks 4 and 5 = MD Weeks 6 and 7 = WD

    Weeks 2 and 3 = MD Weeks 4 and 5 = WD Weeks 6 and 7 = MD

    Outcomes

    Primary Outcome Measures

    Personalized model
    Repeated measures of FCP and GMRS will be used to generate a personalized model identifying food items that provide are predicted to have the greatest effect in the GMRS and FCP levels for a given individual

    Secondary Outcome Measures

    Concentration of FCP levels over time during each intervention
    fecal calprotectin will be analyzed from all stool samples collected during the study to provide continual data on any changes in intestinal inflammation
    Modulation of GMRS over time during each intervention
    Microbiome data will be collected from all stool samples collected during the study to provide continual data on any changes. This data will be used to calculate the GMRS at each time point. A higher GMRS indicate high risk for Crohn's disease
    Measure of microbial taxa relative abundance over time during each intervention
    Microbiome data will be collected from all stool samples collected during the study to provide continual data on any changes in microbial composition
    Ability to maintain a balanced diet as measured by food intake records
    Through the submission of the daily food diaries an assessment on the ability to maintain the diet will be reviewed
    Adherence to the interventions
    Compliance to the diet will be monitored through an app throughout the study

    Full Information

    First Posted
    September 16, 2022
    Last Updated
    October 17, 2022
    Sponsor
    Mount Sinai Hospital, Canada
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    1. Study Identification

    Unique Protocol Identification Number
    NCT05566587
    Brief Title
    Designing a Personalized Diet to Reduce the Risk of Crohn's Disease Onset
    Official Title
    Designing a Personalized Diet to Reduce the Risk of Crohn's Disease Onset
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    October 2022
    Overall Recruitment Status
    Not yet recruiting
    Study Start Date
    October 2022 (Anticipated)
    Primary Completion Date
    March 2024 (Anticipated)
    Study Completion Date
    March 2024 (Anticipated)

    3. Sponsor/Collaborators

    Responsible Party, by Official Title
    Principal Investigator
    Name of the Sponsor
    Mount Sinai Hospital, Canada

    4. Oversight

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

    5. Study Description

    Brief Summary
    The purpose of this trial is to run a pilot study that examines the impact of different dietary components on risk factors such as the Genetic, Environmental, Microbial (GEM) Microbiome Risk Score (GMRS) and fecal calprotectin (FCP), a marker of inflammation in the bowels, and a risk factor for developing Crohn's disease (CD) among first degree relatives (parents, siblings, or offspring) of Crohn's patients. The study will utilize the Western diet and the Mediterranean diet to explore the complex interplay between diet, microbiome, and inflammatory biomarkers to identify specific dietary components that may be beneficial in reducing the risk of developing CD. The study will enroll 30 participants from Mount Sinai Hospital in Toronto.
    Detailed Description
    This study is a clinical trial that will occur at Mount Sinai Hospital and healthy first degree relatives of CD patients will be recruited. Participation will occur over 7 weeks with 1 week of consuming the subject's regular diet and 6 weeks of intervention. A total of 30 subjects are expected to be enrolled into this trial. As part of this trial, The study will attempt to modify dietary consumption between the Western Diet (WD) and the Mediterranean Diet (MD) to evaluate participants responses to specific food items key to the WD or MD by monitoring subject's GMRS and FCP. Subjects will be randomized into one of two groups (1:1), in which there will be crossover between the two diets. Stool samples will be collected 3 times a week, a daily questionnaire and a daily consumption diary will be completed through an app. Group 1 will follow the WD for weeks 2 and 3, switch to the MD for weeks 4 and 5, and then back to the WD for weeks 6 and 7. Group 2 will follow the MD for weeks 2 and 3, switch to the WD for weeks 4 and 5, and then back to the MD for weeks 6 and 7. Meal plans developed by the study Dietitian and recipes will be provided for all weeks of the intervention (weeks 2-7). These meal plans will be identical for subjects within the same group. Groceries required to prepare the meals as per the meal plan will be provided to subjects on a weekly basis.

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    Diet, Healthy, High Risk

    7. Study Design

    Primary Purpose
    Prevention
    Study Phase
    Not Applicable
    Interventional Study Model
    Crossover Assignment
    Masking
    None (Open Label)
    Allocation
    Randomized
    Enrollment
    30 (Anticipated)

    8. Arms, Groups, and Interventions

    Arm Title
    Western to Mediteranean to Western Diet
    Arm Type
    Other
    Arm Description
    Weeks 2 and 3 = WD Weeks 4 and 5 = MD Weeks 6 and 7 = WD
    Arm Title
    Mediteranean to Western to Mediteranean Diet
    Arm Type
    Other
    Arm Description
    Weeks 2 and 3 = MD Weeks 4 and 5 = WD Weeks 6 and 7 = MD
    Intervention Type
    Other
    Intervention Name(s)
    Mediteranean to Western to Mediteranean Diet
    Intervention Description
    week 2-3 : Switching between Mediterranean diet and Western diet week 4-5 : Switching between Western diet and Mediterranean diet week 6-7 : Switching between Mediterranean diet and Western diet
    Intervention Type
    Other
    Intervention Name(s)
    Western to Mediteranean to Western Diet
    Intervention Description
    week 2-3 : Switching between Western diet and Mediterranean diet week 4-5 : Switching between Mediterranean diet and Western diet week 6-7 : Switching between Western diet and Mediterranean diet
    Primary Outcome Measure Information:
    Title
    Personalized model
    Description
    Repeated measures of FCP and GMRS will be used to generate a personalized model identifying food items that provide are predicted to have the greatest effect in the GMRS and FCP levels for a given individual
    Time Frame
    7 weeks
    Secondary Outcome Measure Information:
    Title
    Concentration of FCP levels over time during each intervention
    Description
    fecal calprotectin will be analyzed from all stool samples collected during the study to provide continual data on any changes in intestinal inflammation
    Time Frame
    Duration of each diet (2 to 4 weeks)
    Title
    Modulation of GMRS over time during each intervention
    Description
    Microbiome data will be collected from all stool samples collected during the study to provide continual data on any changes. This data will be used to calculate the GMRS at each time point. A higher GMRS indicate high risk for Crohn's disease
    Time Frame
    Duration of each diet (2 to 4 weeks)
    Title
    Measure of microbial taxa relative abundance over time during each intervention
    Description
    Microbiome data will be collected from all stool samples collected during the study to provide continual data on any changes in microbial composition
    Time Frame
    Duration of each diet (2 to 4 weeks)
    Title
    Ability to maintain a balanced diet as measured by food intake records
    Description
    Through the submission of the daily food diaries an assessment on the ability to maintain the diet will be reviewed
    Time Frame
    6 weeks
    Title
    Adherence to the interventions
    Description
    Compliance to the diet will be monitored through an app throughout the study
    Time Frame
    6 weeks

    10. Eligibility

    Sex
    All
    Minimum Age & Unit of Time
    18 Years
    Maximum Age & Unit of Time
    35 Years
    Accepts Healthy Volunteers
    Accepts Healthy Volunteers
    Eligibility Criteria
    Inclusion Criteria: Healthy, asymptomatic first degree relative (child or sibling) of someone with Crohn's disease Have at least 1 bowel movement every other day Exclusion Criteria: Received antibiotic treatment within 3 months of recruitment Unintentional weight loss in the last 3 months more than 15% of baseline weight Have ever been diagnosed with any chronic or recurring gastro-intestinal disease or bowel disease Belly pain occurred more than once per week for longer than three months in the past year Diarrhea (>three times per day) has been occurring for more than three months in the last year Have blood in their stool with most stools Diagnosed with diabetes Diagnosed with Celiac disease Diagnosed with irritable bowel syndrome Diagnosed with inflammatory bowel disease Presents significant symptoms of gastrointestinal disease Pregnant or breastfeeding women Has any serious food allergies Diagnosed with lactose intolerance Unable to stop NSAID or probiotic use during the study
    Central Contact Person:
    First Name & Middle Initial & Last Name or Official Title & Degree
    Williams Turpin, PhD
    Phone
    416-586-4800
    Ext
    2086
    Email
    wturpin@lunenfeld.ca
    First Name & Middle Initial & Last Name or Official Title & Degree
    Heather MacAulay, BSc, BSc
    Phone
    416-586-4800
    Ext
    8451
    Email
    hmacaulay@lunenfeld.ca
    Overall Study Officials:
    First Name & Middle Initial & Last Name & Degree
    Kenneth Croitoru
    Organizational Affiliation
    MOUNT SINAI HOSPITAL
    Official's Role
    Principal Investigator

    12. IPD Sharing Statement

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    Designing a Personalized Diet to Reduce the Risk of Crohn's Disease Onset

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