Comorbidity Management in Rheumatic Disease.

NCT ID: NCT06579222

Last Updated: 2025-10-07

Study Results

Results pending

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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Recruitment Status

RECRUITING

Clinical Phase

NA

Total Enrollment

199 participants

Study Classification

INTERVENTIONAL

Study Start Date

2025-05-01

Study Completion Date

2026-12-19

Brief Summary

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Rheumatoid arthritis is a disease where the immune system attacks the body by mistake, causing inflammation of the joints and other body parts. People with rheumatoid arthritis are at higher risk of infections, heart problems, and bone issues compared to others. They regularly see rheumatologists, arthritis care physicians, to manage their disease. However, managing these other health problems alongside their main treatment is difficult for rheumatologists due to limited resources. This clinical study is being conducted to see if adding a family doctor to a team of rheumatologists can help. Rheumatologists will complete a case report form about the patient's health and send them to a special family physician clinic. This clinic will focus on improving vaccination against diseases, heart health, and bone strength. They will check if patients need special vaccines to protect them from infections. They will screen for heart disease using blood pressure measurements, and order blood work for high cholesterol and diabetes if needed. They will also review bone health and send people for tests to check their bone density if needed. A change in routines and medications may be recommended after their checkup. Rheumatologists will complete another case report about the patient's health 6 months after their family doctor appointment. The study will assess how these markers of health management improve after this family doctor joins the team. It hopes to prove that this new way of working in the community will give people with rheumatoid arthritis better protection against certain infections, heart problems and weak bones.

Detailed Description

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Conditions

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Rheumatoid Arthritis Comorbidities and Coexisting Conditions

Study Design

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Allocation Method

NA

Intervention Model

SINGLE_GROUP

Primary Study Purpose

SUPPORTIVE_CARE

Blinding Strategy

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).

Group Type EXPERIMENTAL

Primary Care Rheumatology Family Physician Consultation

Intervention Type OTHER

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.

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

* Patients of the Waterloo Rheumatology Community Clinic
* 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

* Age less than 18 years or greater than 80 years
* 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
Minimum Eligible Age

18 Years

Maximum Eligible Age

80 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Canadian Rheumatology Association (CIORA)

UNKNOWN

Sponsor Role collaborator

Western University, Canada

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Cassandra Schulz

Role: PRINCIPAL_INVESTIGATOR

Western University

Locations

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Waterloo Rheumatology

Waterloo, Ontario, Canada

Site Status RECRUITING

Countries

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Canada

Central Contacts

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Cassandra Schulz, MD

Role: CONTACT

(519) 279-4047

Facility Contacts

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Cassandra Schulz, MD

Role: primary

(519) 279-4047

Other Identifiers

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125677

Identifier Type: -

Identifier Source: org_study_id

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