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Behavioural Intervention
Family Physician Consultations for Rheumatoid Arthritis
N/A
Waitlist Available
Led By Cassandra Schulz
Research Sponsored by Western University, Canada
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Participants will be patients of the Waterloo Rheumatology Community Clinic, aged 18 to 80 years of age, with a diagnosis of rheumatoid arthritis
Be older than 18 years old
Must not have
Age less than 18 years or greater than 80 years
Significant cognitive impairment that impedes ability to engage in the study or unwilling to participate in the study
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 6 months
Awards & highlights
No Placebo-Only Group
Summary
This trial aims to see if adding a family doctor to a team of rheumatologists can help improve the overall health of people with rheumatoid arthritis. The family doctor will focus on vaccinations, heart
Who is the study for?
This trial is for people with rheumatoid arthritis, a condition where the immune system mistakenly attacks the body. Participants should be seeing a rheumatologist regularly and need help managing related health issues like infections, heart problems, and bone strength.
What is being tested?
The study tests if adding a family doctor to the patient's healthcare team improves management of comorbidities in rheumatic diseases. It involves special consultations focusing on vaccinations, heart health screenings, and bone density assessments.
What are the potential side effects?
Since this trial focuses on consultation rather than medication or invasive procedures, there are no direct side effects from interventions being studied. However, changes in routines or medications recommended after checkups could have their own side effects.
Eligibility Criteria
Inclusion Criteria
You may be eligible if you check “Yes” for the criteria belowSelect...
I am 18-80 years old with rheumatoid arthritis and a patient at the Waterloo Rheumatology Clinic.
Exclusion Criteria
You may be eligible for the trial if you check “No” for criteria below:Select...
I am younger than 18 or older than 80.
Select...
I am able to understand and willing to participate in the study.
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ 6 months
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~6 months
Treatment Details
Study Objectives
Study objectives can provide a clearer picture of what you can expect from a treatment.Primary study objectives
Care Gap: Cardiovascular screening
Care Gap: Osteoporosis screening
Care Gap: Pneumococcal vaccination
Secondary study objectives
Care Gap: Comorbidity treatment with medication
Care Gap: vaccine-preventable diseases (herpes zoster, influenza and COVID-19)
Awards & Highlights
No Placebo-Only Group
All patients enrolled in this study will receive some form of active treatment.
Trial Design
1Treatment groups
Experimental Treatment
Group I: Comprehensive Comorbidity ClinicExperimental Treatment1 Intervention
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).
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Who is running the clinical trial?
Canadian Rheumatology Association (CIORA)UNKNOWN
Western University, CanadaLead Sponsor
252 Previous Clinical Trials
58,293 Total Patients Enrolled
Cassandra SchulzPrincipal InvestigatorWestern University
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