Research is a key part of how we improve care. Many of the tests, treatments, and tools used in hospitals today were created by working with patients who chose to take part in research. 

If you are thinking about joining a study, this page will help you understand what that means and how to learn more. 

What is clinical research? 

Clinical research includes clinical trials and other types of health studies. 

Clinical trials test new treatments, medications, devices, or ways of delivering care. 

Other studies may look at how diseases develop, how care can be improved, or how people experience illness and treatment. 

Some studies involve a new drug or device. Others may involve surveys, interviews, reviewing health records, or comparing existing treatments. 

All research at our hospital follows strict standards, and each study must be reviewed and approved by a Research Ethics Board before it can begin. 

Why take part in research? 

People choose to take part in research for many reasons. 

Possible benefits for you 

  • Access to new treatments or approaches that are not yet widely available 
  • Extra monitoring or follow-up related to the study 
  • A chance to learn more about your condition 
  • The opportunity to play an active role in your care 

Not every study will benefit you directly. The research team will explain potential outcomes and impacts before you decide. 

Benefits for other patients and the future of health care 

  • Helps doctors and researchers improve care 
  • Contributes to safer and more effective treatments 
  • Supports better health for future patients and families 
  • Advances medical knowledge in Ontario and beyond 

Many medical advances are only possible because patients chose to participate in research. 

What does participation involve? 

Each study is different. Before you join, the research team will review a document called an informed consent form with you. This explains: 

  • The purpose of the study 
  • What you will be asked to do 
  • How long the study will last 
  • Possible risks and benefits 
  • How your privacy will be protected 

You will have time to ask questions. You can also take the information home and discuss it with family, friends or your healthcare provider. 

Learn more about clinical trial eligibility and the clinical trial process on the N2 (Network of Networks) webpage

Other common questions 

How are participants treated in a research study?

Participants are treated with the same care and respect as any patient. Research teams follow clear safety rules and ethical standards. 

Do I have to take part if my doctor asks?

No. Participation is always voluntary. Your care will not be affected if you say no. 

Can I leave a study after I join?

Yes. You can withdraw at any time, for any reason, without affecting your care. 

Will my personal health information be shared?

Your information is protected by privacy laws. Research teams remove identifying details whenever possible and store data securely. 

Will it cost me anything?

Most studies do not have costs for participants. The research team will explain any possible expenses before you agree. 

The first step to participating in clinical research is to learn about available opportunities. 

View current research opportunities here