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Study Recruitment

Study Recruitment

Through studies such as these, arthritis will be better understood and new and improved approaches to management will be identified and implemented. We hope to:

  • link you with Canadian researchers who are using the Internet, telephone or mail to conduct national arthritis research;
  • provide you with opportunities to participate in research studies in your geographic region, if available
  • provide an opportunity for people with arthritis from across Canada to be able to participate in arthritis research from the comfort of their homes.

Please note: The research studies listed on this site have received ethics committee approval. The opportunities posted here do not include clinical trials.

How can I submit my study?

Download the Patient Study Checklist [PDF] and submit it to / 1.800. 321.1433. Please note that we will not post opportunities that do not meet the criteria set out in our policy.

Current Studies

  • Inside Trials - An interview of clinical trials and clinical reporting

    Researchers are inviting individuals with arthritis who have previously taken part in a clinical trial of a prescription drug to participate in an interview study to share their experiences of taking part in a trial.

    Why participate in this study? Patients play a key role in research as participants in clinical trials and learning about trials from the patient perspective is important for improving arthritis research. We are interested to learn more about the experiences and views of people who have taken part in a clinical trial. As part of the study, we would like to find out how trial participants view the importance of publishing the results of trial research.

    Those who can take part in the study have:

    • Participated in a clinical trial of a prescription drug prior to the last 12 months and within the last 5 years,
    • participated in the trial as a patient with arthritis or another health condition (rather than as a “healthy volunteer”), and 
    • were 18 years or older when participating in the trial.

    Participating in this study would involve taking part in an interview of about 60 minutes and possibly a 30-minute follow-up interview. Interviews will be held in Victoria and Vancouver. In order to acknowledge the time taken to participate in this project, each participant will receive an honorarium of $50. 

    Additional information about the study: The study will also involve interviews with clinical trial investigators, university administrators, research ethics board members and individuals who have participated in other types of clinical drug trials to provide additional perspectives on clinical trials and trial reporting. The closing date of the project is August 31, 2021.

    Contact Details: Those interested in participating or finding out more information can contact Co-Investigator Richard Morrow at or visit

    This study received ethics approval (#H18-03458) through the University of British Columbia
    Behavioural Research Ethics Board.

  • Project OM: online stress management for preoperative patients

    Principal Investigators: 

    • Madelaine Gierc, MPH, PhD (Kinesiology), PhD Candidate (Clinical Psychology), Department of Psychology, Queen’s University;
    • Dean Tripp, PhD, Associate Professor, Departments of Psychology, Anesthesiology, & Urology, Queen’s University.

    Study Purpose: The vast majority of surgery patients experience stress, worry, and/or anxiety before their operation (“preoperative distress”). Not only can these feelings be unpleasant, but they are also associated with increased risk of experiencing a negative health event. The purpose of this study is to test the effectiveness of an online stress management program for lessening preoperative distress in patients preparing for knee, hip, or shoulder surgery.

    Questions about study and to get involved: If you have any questions, or want to get involved, do not hesitate to contact the research team at We will respond to your e-mail within 48 hours.

    This research protocol has been reviewed for ethical compliance by the Queen's University Health Sciences and Affiliated Teaching Hospitals Research Ethics Board (HSREB).

    Research Ethics: For ethics concerns please contact the Queen’s University Health Sciences and Affiliated Teaching Hospitals Research Ethics Board (HSREB) at 1-844-535-2988 (Toll free in North America) or For research conducted outside of North America use: 1-613-533-2988. Please note: if non-English speaking participants wish to contact the Chair for ethics concerns, translation assistance may be necessary, as the REB Chairs communicate in English only.

  • @Work: A study of millennials with rheumatic conditions

    What support do you need at work? Help us develop recommendations for employers. If you're 18-35 & live with juvenile arthritis, lupus or another rheumatic condition, we want to hear from you.

    Learn more:

  • Coronary artery disease and inflammatory arthritis

    Coronary artery disease (CAD) is more common in women with inflammatory arthritis. Inflammatory arthritis pain can present as chest and shoulder pain and is difficult to distinguish from cardiac pain.

    If you are a woman greater than 55 years of age with rheumatologist diagnosed inflammatory arthritis (rheumatoid psoriatic or ankylosing spondylitis) and established CAD (history of MI, percutaneous intervention [PCI], and/or coronoary artery bypass graft surgery) and interested in participating in a focus group to inform the development of an innovative mobile and web-based health solution for women, please contact Dr. Monica Parry.

    Contact details:

    Dr. Monica Parry, University of Toronto
    (416) 946-3561

    Sessions will be one hour in length. Refreshment and a $25 gift card will be provided.

    This research project received ethics approval (#34908) through the University of Toronto Research Ethics Committee.

  • Exercise & Rheumatoid Arthritis

    Do you have rheumatoid arthritis? Do you want to be more active?

    Researchers at McGill/MUHC are comparing the effects of two different 12-week exercise programs designed for people with RA.

    • Adults 18 to 65 years of age who are not currently exercising
    • Individually supervised exercise program or home-based exercise program
    • Measurement of body composition, resting metabolic rate, muscle strength and other fitness measures before and after the program
    • Participants stay on all usual RA medicines throughout the study

    For more info:

    Call Alex at 514-398-4184 ext 8910

    This research project received ethics approval (##2018-3192) through the McGill University Health Centre Research Ethics Board.

  • Expectations and educational needs of Canadian rheumatologists, rheumatology fellows and patients in the field of precision medicine

    Principal investigator:  
    Doctor Laetitia Michou, MD, PhD, Rheumatologist CHU de Québec-Université Laval

    Doctor Louis Bessette, MD, MSc, FRCPC, Rheumatologist CHU de Québec-Université Laval,  
    Doctor Paul R. Fortin, MD, MPH, FRCPC, Rheumatologist CHU de Québec-Université Laval,  
    Doctor Diane Lacaille, MD, MPH, FRCPC, Rheumatologist Arthritis Research Canada, Vancouver,  
    Doctor Joyce Dogba, MD, PhD, Université Laval,
    Jean Légaré, Ph.D, Arthritis Consumer Advisory Board (PIRA),
    Doctor Sophie Ruel-Gagné, Fellow in rheumatology  

    Project Information:   
    Precision medicine, a personalized medicine based on biomarkers, is a booming field. In recent years, there have been a number of global initiatives such as the Human Genome Project, the 100,000 Genomes Project in the United Kingdom and the US Precision Medicine Initiative whose purpose is to offer personalized care to each individual. Pharmacogenomics, a discipline that studies the role of genes in drug response and drug toxicity, is an important part of precision medicine. Some genetic tests are already widely prescribed by rheumatologists to improve patient care, and new tests should gradually appear and help make better treatment decisions.  

    Some studies have also focused on the knowledge and expectations of patients, but none have been done in rheumatology. They demonstrated that patients generally have a favorable attitude to the integration of precision medicine into clinical practice, but that their knowledge and understanding of genetic principles and tests are limited. It is therefore essential to better inform patients so that they are able to consent in a free and informed manner and to understand the results of the tests so as to integrate them into their shared decision-making. This project will assess the expectations and educational needs in the field of precision medicine among patients with rheumatic diseases, with the intent to develop educational tools that meet their needs. 

    Your Participation:   
    For this project, you will have to complete a 20–question survey divided into four sections: experience, knowledge, expectations and educational needs in the field of precision medicine (the estimated time to complete the questionnaire is 10 minutes). 

    Contact Information: 
    If you have questions about the research project, please contact Sophie Ruel-Gagné (, co-investigator of this project. 

    This study has been approved by the CER du CHU de Québec-Université Laval, #2018-4065

  • Referral to rheumatologists by physiotherapists to enhance access to care: ability and acceptability.

    Principal investigators: Debbie Feldman, PhD, Université de Montréal, Sasha Bernatsky, MD PhD, Université McGill, Linda Woodhouse, PhD, University of Alberta 

    Project description and objectives: Our project, funded by the Canadian Initiative for Outcomes in Rheumatology Care (CIORA) of the Canadian Rheumatology Association focuses on the identification process by physiotherapists of newly affected patients with  inflammatory arthritis and the consequences of rapid referral of these patients to rheumatology care. The purpose of the focus groups is to explore how to facilitate appropriate referrals in rheumatology and optimize the care of a patient with inflammatory arthritis. The focus group will be composed of 4-8 patients and the main goal is to help optimize patient care in inflammatory arthritis. 

    If you are interested in further details about this research, please contact Tatiana Rodriguez, 

    Read the Invitation
  • The Motherhood and Chronic Illness (MaCI) mixed methods cohort study

    Study Leads:

    • Kathleen Chaput, PhD, Assistant Professor, Department of Obstetrics and Gynecology, University of Calgary
    • ​Natalie Scime, MSc, PhD Candidate, Department of Community Health Sciences, University of Calgary

    BACKGROUND: The Motherhood and Chronic Illness (MaCI) study is being done to address a gap in knowledge about the experiences and outcomes of mothers with chronic illness and their children from pregnancy to early childhood, with a special focus on infant feeding. Findings from this study can be used to raise awareness of the needs and experiences of mothers with chronic illness, and to design appropriate materials and services that promote maternal, child, and family health.

    WHAT IS THE PURPOSE OF THE STUDY? The primary purpose of this study is to investigate what factors and support experiences influence infant feeding among mothers with chronic illness in Alberta. Our team is also interested in studying topics such as medication and health service use, physical and mental health, and labour and delivery outcomes among mothers with chronic illness and their children.

    ELIGIBILITY: To be eligible for the MaCI Study, you must be: 

    • Less than 32 weeks pregnant with one baby 
    • Aged 18 or older
    •  Living with at least one pre-existing physical health condition (including forms of arthritis)
    • Planning to try breastfeeding or expressing breast milk for your baby 
    • A resident of Alberta 
    • Comfortable completing online questionnaires in English

    Over the next two years, we are planning to enroll 400 pregnant women with pre-existing physical health conditions from across Alberta into the MaCI study. Each participant will be invited to complete 3 web-based questionnaires, which take about 30 minutes each, starting in pregnancy and up to the first 6 months after their baby is born. The study can be completed entirely online, through email and the internet, and participants will receive a gift card as a thank you for each questionnaire completed.

    To learn more and sign up, please contact:
    Natalie Scime

    Ethics ID-REB19-0443 Study Title-The Motherhood and Chronic Illness (MaCI) study, PI-K.Chaput, Version number/date: 4.0 September 2019. This study has been approved by the University of Calgary Conjoint Health Research Ethics Board.