Participate in Heart Failure Research

Participate in Research

To realize the promise of a healthy heart, research must explore questions relevant to those living with heart failure, and partner with them in creating new innovations in diagnosis, treatment and care. 

Patients, caregivers, family and community members have a central place in research. We can’t do it without you. 

Your engagement at each stage of research is instrumental to ensuring its relevance and success and in amplifying outcomes.

Why Participate in Research

Being part of research can benefit your health, the well-being of a loved one or help someone you don’t know. 

By participating, you can: 

• Shape and evaluate research projects so they incorporate the lived experience of heart failure
• Learn more about your own health and care to benefit yourself
• Gain access to leading healthcare professionals and cutting-edge treatments, technology, and care
• Contribute to new diagnostic, treatments or care that improve lives of people living with heart failure 
• Some studies may offer participants financial compensation. Please see our Patient Compensation Policy to learn about how we recognize patient partners for their contributions.
  

Types of Engagement in Research

Engaging in research can be much more than consenting to join a study – although that is essential and important as we couldn’t do it without you. You can: 

• Be part of a team developing a research proposal
• Be a lay reviewer on the peer review panel evaluating research proposals 
• Be part of an advisory committee – influencing our priorities and activities as a result of research findings. 
• Be a study participant. 
• Help discuss and promote research findings so more people understand and apply this new knowledge.
  

What to Know Before Engaging as a Study Participant

Many protections are in place to safeguard the rights and safety of research participants. 

However, before you participate in a research study, there are still some things you should make yourself aware of:

• What is the criteria for participation? Are you eligible?
• Has the study been approved by a Research Ethics Board? 
• What is the purpose of the study? Why and how is research being conducted?
• What are the risks associated with participation? 
• How will your privacy be protected?
• Where does the study take place? Is it virtual or in-person?
• Are there costs associated with participation (i.e. travel). If so, will you be reimbursed?
• What are the benefits to participating? Is there compensation available?
• What are the expectations of you as a study participant?
• What is the length of participation/anticipated time commitment?
• Who can you contact for more information or to withdraw?

As a research participant, you are free to withdraw at any time. Your participation is totally voluntary.

To learn more about the different types of clinical trials and how they advance understanding of diseases and how to treat them, check out the Heart Failure Society of America’s (HFSA) Patient Education Module on Clinical Trials. For a more in-depth exploration of the importance of clinical trials and how to participate in them, HFSA also offers a patient-centered tutorial on clinical trials.

Studies in Recruitment at Ted Rogers

To learn about opportunities for people with lived experience to participate in heart failure research at Ted Rogers, visit our Studies in Recruitment page.

To stay informed about new opportunities to participate in research as they come up, please sign up for our newsletter.