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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RECRUITING
NA
199 participants
INTERVENTIONAL
2025-05-01
2026-12-19
Brief Summary
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Detailed Description
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Conditions
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Study Design
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NA
SINGLE_GROUP
SUPPORTIVE_CARE
NONE
Study Groups
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Comprehensive Comorbidity Clinic
The following investigations and treatments will be offered as associated with a comprehensive comorbidity clinic appointment with the primary care rheumatology family physician: Blood pressure, heart rate, height and weight measurement. Blood work (standard lipid panel, fasting plasma glucose or glycated hemoglobin (A1C), eGFR, and Lipoprotein a, Bone densitometry (if applicable to the patient/participant).
Vaccinations will be offered if applicable to the patient/participant according to Health Canada guidelines (Vaccination with Pneu-P-23, Pneu-C-13, herpes zoster and COVID-19 vaccine).
Primary Care Rheumatology Family Physician Consultation
The participant will be booked with a primary care rheumatology family physician for rheumatoid arthritis comorbidity screening. They will complete weight, height, blood pressure measurement, assess for risk factors for dyslipidemia, type 2 diabetes, hypertension, bone mineral density loss and vaccine preventable infectious diseases.
Interventions
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Primary Care Rheumatology Family Physician Consultation
The participant will be booked with a primary care rheumatology family physician for rheumatoid arthritis comorbidity screening. They will complete weight, height, blood pressure measurement, assess for risk factors for dyslipidemia, type 2 diabetes, hypertension, bone mineral density loss and vaccine preventable infectious diseases.
Eligibility Criteria
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Inclusion Criteria
* Aged 18 to 80 years of age
* Diagnosis of rheumatoid arthritis
* Minimum of limited working proficiency in English
* No significant cognitive impairment that can inhibit their ability to engage in the study
Exclusion Criteria
* Significant cognitive impairment that impedes ability to engage in the study
* Unwilling to participate in the study
* Patients currently pregnant will be excluded from the study
18 Years
80 Years
ALL
No
Sponsors
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Canadian Rheumatology Association (CIORA)
UNKNOWN
Western University, Canada
OTHER
Responsible Party
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Principal Investigators
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Cassandra Schulz
Role: PRINCIPAL_INVESTIGATOR
Western University
Locations
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Waterloo Rheumatology
Waterloo, Ontario, Canada
Countries
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Central Contacts
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Facility Contacts
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Other Identifiers
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125677
Identifier Type: -
Identifier Source: org_study_id
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