OCC’S RESEARCH IS PATIENT CENTRED AND WE BELIEVE THAT CLINICAL AND SCIENTIFIC INQUIRY CAN BE ENHANCED BY THE UNIQUE PERSPECTIVES OF THOSE AFFECTED BY THE DISEASE.

OCC’s Patient Partners in Research (PPiR) program was developed in 2020 to ensure the voices of those with lived experience are at the forefront of research. Engaging ovarian cancer patients as partners reflects our philosophy that the relevance, importance, and impact of research can be enhanced with input and viewpoints of those affected by this disease.  

Members of the PPiR team include ovarian cancer patients, previvors, caregivers, or loved ones, each bringing their unique perspective and shared experience to inform research. Members were selected to ensure a diverse representation of ovarian cancer types, age, sexuality, cultural backgrounds, and geography. The program is led by OCC’s Scientific Advisor and Research Coordinator, and patient advocates.    

Emma Gerber, Research Trainee

“I am so glad to have this photo on my lab bench as a reminder of why I do what I do. It helps to keep me grounded when the patients feel so far away from our lab work. To the strong women in this photo and to all of the others navigating this disease: I am honored to dedicate my research to you. You are inspiring and I will work hard to contribute to better outcomes for those with ovarian cancer. Thank you for sharing your stories, your strength, and your light with me! I carry them with me every day.”

OCC educates and trains patients to include their perspective in levels of decision making

“I am an integral part of this research. This patient-centred approach is especially important when it comes to clinical trials, when the patient voice is critical in determining which kinds of trials are going to be most effective. This can lead to better research and changes in clinical care,” says Starla Fiddler, patient partner from Saskatchewan. “I am proud to say that I am one of Ovarian Cancer Canada’s Patient Partners in Research. I take this role very seriously. Did I want cancer? Absolutely not. But if my experience can help just one other person, then that’s all that matters.”

Who can participate?

People diagnosed with ovarian cancer

Previvors (people at increased risk for ovarian cancer)

Caregivers

Family members/loved ones

Why Participate?

The PPiR program complements and maximizes the impact of cancer research conducted by OCC-supported scientists. Our patient-centred research prioritizes questions that are relevant and meaningful to patients and their loved ones.

HELP IMPROVE OUTCOMES

The voice of a patient partner can significantly influence the advancement of ovarian cancer care, improving outcomes for future generations.

LEAVE A LASTING LEGACY

By contributing their personal experience, patient partners make a lasting impact on research, advocacy, and support, leaving behind a legacy of progress.

ENHANCE UNDERSTANDING OF OVARIAN CANCER

The PPiR program facilitates meaningful exchanges between patients and researchers, including early career scientists and research trainees. Through collaboration, patient partners enhance the understanding of the ovarian cancer experience and empower contributions to healthcare.

HOW DO PATIENTS PARTICIPATE?

All members of the PPiR program are required to complete the Science of Cancer online course, in addition to task-specific training dependent on the engagement opportunity. Some examples of activities that PPiR team members participate in include:

  • Serving as patient reviewers on grant funding (pre-clinical and clinical) and trainee award review panels
  • Participating as embedded research team members on OCC-funded projects (both clinical and pre-clinical)
  • Speaking opportunities at OCC events and national and international research conferences
  • Participating in small interactive sessions with researchers and trainees
  • Consulting and co-developing funding proposals, patient surveys, and educational tools
  • Consulting on strategic planning such as program guidelines, research partnership agreements, programmatic design, and patient engagement best practices
  • Participating in graduate student advisory committees
  • Participating in research and system advocacy alongside OCC

Become a Patient partner in research

As a patient partner, you are expected to:

  • Commit to achieving a fundamental understanding of the research process
  • Attend and participate in virtual monthly meetings with scientific experts
  • Complete the mandatory training and task-specific training for various engagement opportunities
  • Participate in engagement opportunities including conferences, symposia, grant review panels, and clinical trial teams
  • Draw on personal experiences to provide insight for research projects
  • Network with researchers and clinicians to build active partnerships
  • Provide OCC with constructive program feedback
  • Maintain confidentiality of all research-related details, as patient partners will be privy to information that is not publicly available

Interested in applying your patient experience to transform lives?

PPiR Expression of interest

Recruitment is currently closed, please complete this form and we will be in touch when re-opened.

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We deserve a voice at the table of researchers, oncologists and scientists. We are the ones undergoing the clinical trials, enduring the side effects of treatments, and putting ourselves on the line in hopes of fighting back against this brutal disease.

Shannon Kadar, Patient Partner