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Inflammatory Bowel Disease Tracker (IBD Tracker) (IBDTr)

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ClinicalTrials.gov Identifier: NCT03953794
Recruitment Status : Not yet recruiting
First Posted : May 17, 2019
Last Update Posted : August 13, 2019
Sponsor:
Collaborators:
Massachusetts Institute of Technology
University Medical Center Groningen
Information provided by (Responsible Party):
Ashwin Ananthakrishnan, Massachusetts General Hospital

Brief Summary:

Inflammatory Bowel Diseases are incurable, life-long conditions that significantly impact a patient's quality of life. Crohn's Disease and ulcerative colitis are the most prevalent inflammatory bowel diseases in the United States; both are characterized by chronic, relapsing inflammation of the intestinal tract, which manifests as symptoms of diarrhea, fecal urgency, fecal incontinence, fever, fatigue, abdominal pain and cramping. These severely debilitating periods of illness or "flare" alternate with times of remission when patients have few or no symptoms, and feel healthy. Despite periodic respite, many patients with IBD experience severe stress and anxiety even when they are well, because of the likely occurrence of episodes of disease in their future. This is exacerbated by the unpredictable frequency and inconsistent duration of flares that may last as long as several weeks or months.

The goal for this study is to use non-invasive monitoring techniques to identify biomarkers that emerge, or change predictably, when a patient begins to relapse from remission to enter a period of disease - to find the earliest signs of an active flare. If the investigators identify a pattern of biomarkers that could alert a patient and their clinician to a flare as soon as it begins, it may be possible to intervene before symptoms present by changing medication and/or diet and lifestyle to lessen the severity of the disease flare. The biomarker fingerprint may also reveal new targets for therapeutics that could control IBD.


Condition or disease Intervention/treatment
Inflammatory Bowel Diseases Ulcerative Colitis Crohn Disease Device: Fitbit Charge 3

  Show Detailed Description

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Study Type : Observational [Patient Registry]
Estimated Enrollment : 100 participants
Observational Model: Cohort
Time Perspective: Prospective
Target Follow-Up Duration: 12 Months
Official Title: Inflammatory Bowel Disease Tracker (IBD Tracker)
Estimated Study Start Date : October 2019
Estimated Primary Completion Date : February 2021
Estimated Study Completion Date : February 2021

Resource links provided by the National Library of Medicine

MedlinePlus related topics: Crohn's Disease

Group/Cohort Intervention/treatment
Patients with inflammatory bowel disease

Patients who have...

  1. a diagnosis of ulcerative colitis or Crohn's disease as confirmed by a clinician
  2. experienced a flare within the past 24 months as determined by a clinician
  3. had quiescent disease for at least 3 months as determined by a clinician
Device: Fitbit Charge 3
Smart watch monitoring activity and movement, heart rate, sleep, and more




Primary Outcome Measures :
  1. Simple Clinical Colitis Activity Index [ Time Frame: 1 week ]

    Patient-reported measure for ulcerative colitis referring to disease symptoms occurring over the last week. The point value from each answer is added up for a total score.

    1. Over the past week, what is your average number of bowel movements during the day (not including night)? (0) 0-3 (1) 4-6 (2) 7-9 (3) >9
    2. Over the past week, what is your average number of bowel movements at night? (0) 0 (1) 1-3 (2) >3
    3. Over the past week, what has been your urgency of defecation? (0) No rush (1) Hurry (2) Immediately (3) Incontinence
    4. Over the past week, what has been the amount and frequency of blood in your stool? (0) None (1) Small traces (2) Occasionally obviously bloody (3) Usually obviously bloody
    5. General well being (0) Very well (1) Slightly below par (2) Poor (3) Very poor (4) Terrible
    6. During the past week, have you had any of the following? (1 pt/answer) (1) Pyoderma gangrenosum (1) Erythema nodosum (1) Uveitis (1) Arthritis (0) None

  2. Harvey-Bradshaw Index [ Time Frame: 1 week ]

    Patient-reported measure for Crohn's disease referring to disease symptoms occurring over the last week. The point value from each answer is added up for a total score.

    1. General well being (0) Very well (1) Slightly below par (2) Poor (3) Very poor (4) Terrible
    2. In the past week, have you experienced any abdominal pain? (0) None (1) Mild (2) Moderate (3) Severe
    3. How many liquid stools do you pass per day? (1 point per liquid stool)
    4. Do you have an abdominal mass? (0) None (1) Dubious (2) Definite (3) Definite and tender
    5. During the past week, have you had any of the following? (1 point per answer) (1) Pyoderma gangrenosum (oozing ulcers, usually on the leg) (1) Erythema nodosum (red, swollen bumps, on the skin (1) Uveitis (red, painful eyes) (1) Aphthous ulcers (mouth ulcers) (1) Arthritis (joint pain) (1) Anal fissue (1) New fistula (1) Perianal abscess (0) None of the above

  3. Stress and Wellbeing [ Time Frame: Current moment in time ]
    Patient-reported measure of current stress level measured on a scale of 1 (1 = no stress) to 5 (5 = highest stress possible)

  4. 24-hour dietary recall survey [ Time Frame: 24 hours ]
    Patient-reported measure of diet over the last 24 hours. The survey can be found here: https://asa24.nci.nih.gov/demo/

  5. Blood biomarkers - metabolite content [ Time Frame: 12 months ]
    Metabolite content will be determined by monitoring patients via regular blood draws over the 12-month study period. By analyzing metabolite content in periods of health (remission), disease (flare), and the transition period in between, investigators hope to identify unique biomarkers that indicate the earliest stages of a flare. The investigators do not know each specific metabolite that will be measured. The objective of this outcome is to identify any and all possible biomarkers and metabolites that may be present in these samples.

  6. Blood biomarkers - cytokine profile [ Time Frame: 12 months ]
    Cytokine profile will be determined by monitoring patients via regular blood draws over the 12-month study period. By analyzing cytokine profile in periods of health (remission), disease (flare), and the transition period in between, investigators hope to identify unique biomarkers that indicate the earliest stages of a flare. The investigators do not know each specific biomarker and cytokine that will be measured. The objective of this outcome is to identify any and all cytokines that may be present in these samples.

  7. Blood biomarkers - T-cell receptor sequence profile [ Time Frame: 12 months ]
    T-cell receptor sequence profiles will be determined by monitoring patients via regular blood draws over the 12-month study period. By analyzing T-cell receptor sequence profiles in periods of health (remission), disease (flare), and the transition period in between, investigators hope to identify unique biomarkers that indicate the earliest stages of a flare.

  8. Stool biomarkers - microbial DNA content in microbiome [ Time Frame: 12 months ]
    Patients will submit weekly stool samples for analysis and monitoring. The investigators will analyze the gut microbiome composition by characterizing the microbial DNA content and tracking changes throughout the 12-month study period. The investigators do not know each microbe that will be assessed. The objective of this outcome is to identify any and all microbes that may be present in these samples.

  9. Stool biomarkers - overall microbiome content [ Time Frame: 12 months ]
    The investigators will analyze the bacterial, fungal, and viral constituents at enrollment and and track changes throughout the 12-month study period to identify biomarkers of importance. These will be assessed with stool wipe samples, glycerol-preserved stool, and fresh and ethanol-preserved stool samples. Stool samples will either collected by patients at home or collected in-clinic and flash frozen.

  10. Stool biomarkers - degree of intestinal inflammation via Fecal Calprotectin [ Time Frame: 12 months ]
    The investigators will measure the degree of intestinal inflammation by quantifying Fecal Calprotectin (a biomarker) levels in patients' weekly stool samples and tracking changes throughout the 12-month study period. This will be measured using stool wipe samples and fresh stool samples.

  11. Urine biomarkers - metabolite content [ Time Frame: 12 months ]
    The investigators will use urine samples collected throughout the study to analyze each subject's urine metabolite content and track changes throughout the 12-month study period in an attempt to identify biomarkers potentially indicative of a flare. The investigators do not know each specific metabolite that will be measured. The objective of this outcome is to identify any and all possible biomarkers and metabolites that may be present in these samples.


Secondary Outcome Measures :
  1. Biospecimen association - microbiome timeseries and blood and stool metabolites [ Time Frame: 12 months ]
    Investigators will measure any existing correlations between the microbiome timeseries and the identified blood and stool metabolites over the 12-month study period to determine if there are any associations between the two variables.

  2. Biospecimen association - microbiome composition and fecal calprotectin levels [ Time Frame: 12 months ]
    Investigators will measure any existing correlations between the microbiome composition and fecal calprotectin levels identified in the primary outcomes over the 12-month study period to determine if there are any associations between the two variables.

  3. Biospecimen association - blood and stool metabolites and microbiome composition [ Time Frame: 12 months ]
    Investigators will measure any existing correlations between the identified blood and stool metabolites and the microbiome composition over the 12-month study period to determine if there are any associations between the two variables.

  4. Biospecimen association - stool metabolites and blood metabolites [ Time Frame: 12 months ]
    Investigators will measure any existing correlations between the identified blood metabolites and the identified stool metabolites and the microbiome composition over the 12-month study period to determine if there are any associations between the two variables.


Biospecimen Retention:   Samples With DNA
Optional blood, stool, and urine samples will be requested at various time points throughout the 12-month follow-up period. Optional biopsy samples can be collected at a standard-of-care endoscopic procedure.


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Ages Eligible for Study:   18 Years and older   (Adult, Older Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Sampling Method:   Non-Probability Sample
Study Population
Adults with established inflammatory bowel disease who have had quiescent disease for at least 3 months but have experienced a flare within the last 24 months
Criteria

Inclusion Criteria:

  • 18 years of age or older
  • Able to provide written informed consent prior to screening and willing to comply with the requirements of the study protocol
  • Have had a diagnosis of ulcerative colitis or Crohn's Disease confirmed by a clinician
  • Have had quiescent disease for the past 3 months or longer as determined by clinician
  • Have had most recent episode of disease within past 24 months as determined by clinician
  • Have had stable IBD medication (other than antibiotics) regimen for the past 3 months or longer
  • Able to speak and read English sufficiently
  • Be able and comfortable using new technology: the app and the smartwatch for 12 months

Exclusion Criteria:

  • If female, is pregnant or is breast feeding, or intends to become pregnant within the 12 month study period
  • Unable to provide informed consent or unwilling to participate
  • Use of oral or intravenous antibiotics within 4 weeks prior to screening
  • Current use of glucocorticoid steroid, or nonsteroidal anti-inflammatory drugs (NSAIDs) within the last 3 months
  • Evidence of untreated infection e.g. Clostridium difficile
  • Confirmed diagnosis of extraintestinal manifestations (EIMs) of disease including those that occur concurrent with colitis (episcleritis, scleritis, uveitis, peripheral arthropathies of small and large joints, dermatologic conditions such as erythema nodosum and pyoderma gangrenosum), and those that occur independent of colitis (sacroilitis, ankylosing spondylitis, or primary sclerosing cholangitis)
  • Confirmed diagnosis of other serious disease unrelated to ulcerative colitis or Crohn's Disease
  • Current smoker
  • Unable to speak or read English

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Responsible Party: Ashwin Ananthakrishnan, Assistant Professor of Medicine, Massachusetts General Hospital
ClinicalTrials.gov Identifier: NCT03953794     History of Changes
Other Study ID Numbers: 2017P002778
First Posted: May 17, 2019    Key Record Dates
Last Update Posted: August 13, 2019
Last Verified: August 2019
Individual Participant Data (IPD) Sharing Statement:
Plan to Share IPD: Undecided

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Studies a U.S. FDA-regulated Drug Product: No
Studies a U.S. FDA-regulated Device Product: No
Additional relevant MeSH terms:
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Crohn Disease
Colitis, Ulcerative
Intestinal Diseases
Inflammatory Bowel Diseases
Gastroenteritis
Gastrointestinal Diseases
Digestive System Diseases
Colitis
Colonic Diseases