Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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WITHDRAWN
OBSERVATIONAL
2019-10-31
2021-02-28
Brief Summary
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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.
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Detailed Description
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According to the Centers for Disease Control and Prevention, there are currently an estimated 1-1.3 million people with IBD in the United States, and most of these patients are diagnosed with the disease before age 30. The burden of living with these lifelong conditions is obviously severe, however the financial burden should also be considered. In 2008, the total annual financial burden for direct treatments costs for patients with IBD in the United States was estimated to be $6.3 billion. Costs includes expenses such as physician services, prescription and over-the-counter drugs, hospitalization, and other direct medical expenses. Indirect costs (including lost earnings or productivity, and lost leisure time) were estimated to amount to an additional $5.5 billion.
Although the study is not targeted at finding a cure for IBD, the goal is to vastly improve the patient's quality of life by identifying biomarkers that emerge, or change predictably in a period leading up to the very beginning of a flare.
The investigators will identify biomarkers that predict an episode of disease is imminent. The investigators will target biomarkers that can be tracked non-invasively, by monitoring changes in the stool microbiome, metabolites in stool and urine, as well as physiological and lifestyle changes by asking patients to wear a wearable device (the Fitbit Charge 3). The investigators will collect blood samples regularly (blood draws are minimally invasive) to monitor additional biomarkers. By intensively monitoring patients in this way for a period of time that encompasses health (remission) and disease (flare), as well as the transition period in between, the investigators hope to amass enough data to tease out such a biomarker, or fingerprint of biomarkers, that benchmark the earliest stages of a flare. The investigators will conduct this study in collaboration with researchers at the Center for Microbiome Informatics and Therapeutics at Massachusetts Institute of Technology.
The ability to non-invasively track biomarkers, to monitor a patient for such an early disease fingerprint, may give that patient the power to manage their lives and their disease with greater precision than they can today. In particular, if that early disease fingerprint appears at a time when the patient still feels well, it is possible they could intervene to block progression of the flare by changing medications, and/or making lifestyle changes thus minimizing the impact of the flare, and the symptoms they experience.
Furthermore, pinpointing the molecular changes that occur systemically, throughout the patients during this transition period, from health (remission) to disease (flare) will give researchers the knowledge and tools with which to begin to develop therapies that can block progression of the disease state, preventing the flare, and perhaps "reset" the body to a state of health. Therapies, like these would greatly relieve the burdens of disease and financial costs for this patient population.
Conditions
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Study Design
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COHORT
PROSPECTIVE
Study Groups
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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
Fitbit Charge 3
Smart watch monitoring activity and movement, heart rate, sleep, and more
Interventions
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Fitbit Charge 3
Smart watch monitoring activity and movement, heart rate, sleep, and more
Eligibility Criteria
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Inclusion Criteria
* 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
* 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
18 Years
ALL
No
Sponsors
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Massachusetts Institute of Technology
OTHER
University Medical Center Groningen
OTHER
Massachusetts General Hospital
OTHER
Responsible Party
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Ashwin Ananthakrishnan
Assistant Professor of Medicine
Other Identifiers
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2017P002778
Identifier Type: -
Identifier Source: org_study_id
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