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Rheumatic DiseasesPOET-RheumNCT07022756

Personalized Outreach for Equitable Treatment in Rheumatology

A study testing Honoraria and Outreach in people with Rheumatic Diseases and Inflammatory Arthritis, run by University of British Columbia at 1 site in Canada.

Not yet recruiting

Opening soon. The study is approved but enrolment has not started yet. Sites may already take enquiries.

Sites and contacts
Official record
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Trial summary

The primary goal of this study is to determine whether providing patient honoraria and/or outreach services can improve the attendance rate of appointments at an inner city rheumatology clinic in Vancouver, British Columbia. Read more about this study

Who is it for?
Ages 18 years and older
What is being tested?
Honoraria and Outreach
Could I receive a placebo?
No, everyone receives an active treatment
How many people
20 participants
Where
1 siteCanada
Study dates
2 Jul 2025to Jun 2026
Phase
Interventional
Are there results?
Not yet: the study is under way

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 years and older
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Who may be able to join

  • Have a diagnosis of inflammatory arthritis secondary to an autoimmune rheumatic disease
  • Be attached to one of the Vancouver Coastal Health Community Health Centres for primary care
  • Be willing to attend in-person appointments at Pender Community Health Centre
  • Be at least 18 years of age and capable of consenting to participation
  • Be able to receive medical care in English.

Who cannot join

  • Have cognitive impairment or an untreated psychiatric condition that would severely impair ability to engage with outreach or treatment
  • Have no reasonably reliable method of contact (phone, email, social media, etc.)

Trial locations and contacts

1 site in 1 country. Contact the study team or a site near you to ask about taking part.

Chu Ming (Alec) Yu, MD contact

778-807-3323

alec.yu@vch.ca

Canada1 site
  • Pender Community Health Centre

    Vancouver, British Columbia

    Chu Ming (Alec) Yu, MD, 778-807-3323, alec.yu@vch.ca

Other trials in Canada

About this study

Official title: Personalized Outreach for Equitable Treatment in Rheumatology: A Randomized Controlled Trial of Patient Outreach and Honoraria in an Inner City Rheumatology Clinic

The primary goal of this study is to determine whether providing patient honoraria and/or outreach services can improve the attendance rate of appointments at an inner city rheumatology clinic in Vancouver, British Columbia.

The main question it aims to answer are:

Read more
  • Does providing a financial honorarium ($20 for each follow-up appointment with completed bloodwork) improve attendance rate at an inner city rheumatology clinic?
  • Does providing a personalized outreach service for rheumatic diseases improve attendance rate at an inner city rheumatology clinic?

The researchers will compare providing patient honoraria to providing both honoraria and outreach services, and compare each of these to the regular appointment schedule without honoraria or outreach.

Participants will:

  • Undergo randomization to receive honoraria or honoraria and outreach services together
  • Complete surveys about their health and understanding of their rheumatic disease at baseline, 3-month, and 6-month intervals
  • Visit the clinic every month for check-ups and monitoring bloodwork if they are started on immunosuppressants for their condition
Read the detailed description

Our study aims to enhance the existing twice-monthly rheumatology clinic at the Pender Community Health Centre with a rheumatology-specific outreach service for patients with inflammatory arthritis. This service will be provided by a rheumatology subspecialty trainee under the supervision of two attending rheumatologists. This will consist of biweekly phone calls, text messages, or home visits as per the patient's preference, at times flexible to patient needs. This will be in addition to monthly in-person assessment and bloodwork monitoring with adjustment as clinically indicated by their treating rheumatologist. Outreach services will include management of medications and side effects, proactive screening for infections, coordination of rheumatologic and general healthcare with their Primary Care Provider, social service navigation, and reminders for appointments and lab monitoring. All participants will be provided with a $20 honorarium for each in-person assessment they attend as part of the study.

The investigators will aim to enroll 20 participants between July 2025 and October 2025. Participants will be randomized to either honorarium with outreach or honorarium alone arms in a 1:1 fashion, stratified by housing status (unhoused and emergency sheltered in one strata, provisionally accommodated and stably housed in the second strata).

All enrolled participants will receive a $20 honorarium for each in-person assessment with completed monitoring bloodwork as requested by the treating rheumatologist. The program will last 6 months for each patient from time of enrolment, or until a patient chooses to leave the program, whichever is sooner. At baseline, participants will complete two surveys: one on their general health status, and one specific to their rheumatic disease. At the 3-month and 6-month visits, these surveys will be repeated, and a semi-structured interview will be completed to obtain feedback on the pilot program.

The outcomes of this study will inform how rheumatologists can better care for those who live with inflammatory arthritis and are also marginalized by extreme poverty and/or housing instability. The investigators plan on disseminating and discussing results with our participants, community members, inner city physicians, and rheumatologists. If there are specific positive themes or outcomes from the study, the investigators will advocate for additional resources to permit long-term implementation and further study to confirm results, make further improvements to our program, and improve generalizability.

Being tested
Honoraria, Outreach
Keywords
Rheumatology, Inflammatory Arthritis, Inner City Health
Medical subject headings
Rheumatic Diseases, Arthritis, Arthritis, Rheumatoid, Arthritis, Psoriatic, Connective Tissue Diseases

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • HonorariaBehavioural

    A $20 honorarium for each appointment attended with completed bloodwork if requested.

  • OutreachBehavioural

    A personalized outreach service specific for rheumatic disease.

Study groups in NCT07022756
Study groupRoleWhat they receive
Honoraria OnlyActive comparatorParticipants in this arm of the study will only receive honoraria and not outreach
Receives: Behavioral: Honoraria
Honoraria and OutreachExperimentalParticipants in this arm of the study will receive both honoraria and outreach services
Receives: Behavioral: Honoraria; Behavioral: Outreach
Historical ControlNo interventionThe attendance rate to follow-up appointments among all patients with inflammatory arthritis due to a rheumatic disease at the Pender Rheumatology Clinic from Jan 2023 to Jun 2025.

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Attendance at in-person follow-up appointments

    Adherence to in-person follow-up measured by the ratio of appointments attended to appointments scheduled.

    Measured: Cumulative over 6 months

Secondary outcomes (4)
  1. Clinical Disease Activity Index (CDAI)

    The change in Clinical Disease Activity Index from baseline to 3-months and 6-months. The Clinical Disease Activity Index is a validated disease outcome measure in Inflammatory Arthritis ranging from 0 to 76. A higher score means a worse outcome.

    Measured: 3-month and 6-month intervals.

  2. Patient Qualitative Feedback

    Patient qualitative feedback on the program via semi-structured interview.

    Measured: 3-month and 6-month intervals.

  3. Patient Reported Understanding of Disease and Medications

    Patient Reported Understanding of Disease and Medications, as measured by likert scale at baseline, 3 months, and 6 months. The likert scale will range from 1 to 10, with higher scores indicating better understanding.

    Measured: 3-month and 6-month intervals.

  4. Patient reported pain related to arthritis

    Patient reported pain related to arthritis on a visual analogue scale. The visual analogue scale is a validated measure of pain in arthritis, where participants are asked to indicate their severity of pain within the previous week on a 0 to 100mm score. A score of 0 indicates "no pain", and a score of 100 indicates "worst possible pain".

    Measured: 3-month and 6-month intervals

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted15 Jun 2025
  2. Study start2 Jul 2025 (estimated)
  3. Primary completionApr 2026 (estimated)
  4. Study completionJun 2026 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Health services research
Allocation
Randomised
Intervention model
Parallel groups
Masking
None (open label)
Enrolment
20 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT07022756
Sponsor's protocol ID
H24-03984
Acronym
POET-Rheum
Status last verified
Jul 2025
First submitted
7 Jun 2025
Last updated
4 Jul 2025
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No: We are working with a uniquely vulnerable population who are marginalized by extreme poverty, and feel that the risks of identification by sharing individual patient data outweigh the academic benefits in this study.

Questions about this trial

What is this clinical trial studying?

A study testing Honoraria and Outreach in people with Rheumatic Diseases and Inflammatory Arthritis, run by University of British Columbia at 1 site in Canada.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 5 inclusion and 2 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: opening soon, as of the sponsor's last update on 4 Jul 2025. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in Canada. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

This study is still under way. Results are not available in the source record yet.

How can a doctor refer a patient or contact the research team?

Contact Chu Ming (Alec) Yu, MD (778-807-3323, alec.yu@vch.ca), or a site near the patient. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Attendance at in-person follow-up appointments (time frame: Cumulative over 6 months). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 4 Jul 2025.

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