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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COMPLETED
164 participants
OBSERVATIONAL
2005-09-01
2011-12-12
Brief Summary
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Detailed Description
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Conditions
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Study Design
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COHORT
PROSPECTIVE
Eligibility Criteria
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Inclusion Criteria
* Current active, adult-onset rheumatoid arthritis who meet American College of Rheumatology (ACR) criteria for RA and have: (ACR functional class I-III), defined as:
* 3 or more swollen or tender joints and
* Morning stiffness of 45min or longer
* OR judged by their rheumatologist to have active disease
* No evidence of other inflammatory diseases (e.g., Crohn's, IBS)
* Functional class I, II or III
Exclusion Criteria
* Unwilling to have medications monitored and/or comply with protocol
* Not fluent in English
* Planning to move from area within next year or change health insurance (which would preclude ongoing care by a Johns Hopkins rheumatologist)
* Enrolled in study evaluating efficacy of new or existing RA medications
19 Years
ALL
No
Sponsors
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Johns Hopkins University
OTHER
Responsible Party
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Principal Investigators
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Susan Bartlett, PhD
Role: PRINCIPAL_INVESTIGATOR
Johns Hopkins School of Medicine
Cynthia S Rand, PhD
Role: PRINCIPAL_INVESTIGATOR
Johns Hopkins University
Locations
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Johns Hopkins Bayview Campus
Baltimore, Maryland, United States
Countries
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Other Identifiers
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NA_00001359
Identifier Type: -
Identifier Source: org_study_id