
PROJECTS
Survey Closed - Reopening Summer 2026
The Future of Psychedelic-Assisted Cancer Care
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Are You...
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A person living with or beyond cancer?
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A caregiver supporting someone with cancer?
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A clinician working in oncology from any discipline?
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A healthcare policymaker?
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A member of a community support provider?
If yes, and you are
18 years or older
& residing in Canada,
we want to hear from you!

The Priority Setting Partnership Survey is currently closed.
In Round 1 of the Priority Setting Partnership Survey, we invited specific voices—patients, caregivers, clinicians, and decision-makers—to help identify and prioritize unanswered questions in psychedelic-assisted cancer therapy. This first phase focused on gathering a broad range of perspectives to better understand what matters most to those directly impacted.
The survey is now closed, and we are preparing for the next stage. Round 2 will open in late summer or early fall 2026, where participants will be invited to review and help prioritize the questions identified in Round 1. To learn more about the James Lind Alliance and their priority settings partnership approach, see below.
Please check back for updates or sign up for notifications when recruitment reopens.
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James Lind Alliance (JLA) Priority Setting Partnership (PSP)

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The James Lind Alliance (JLA) brings together patients, caregivers, and healthcare professionals to find out what research questions matter most to them.
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Instead of researchers deciding what to study, the JLA makes sure that the people most affected by a health condition have a real voice.
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Through a fair and transparent process, the JLA helps groups identify and rank the top unanswered questions about treatments and care. These "Top 10 Priorities" guide future research so it meets real-world needs.

At CAN-PACT, we’re using the JLA’s proven approach to make sure our research focuses on what matters most to people living with advanced cancer.
Learn more about JLA here:
Interested in Learning More about JLA?
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What does the JLA process look like?
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Build a team of patients, caregivers, and clinicians.
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Gather important unanswered questions.
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Refine and review the questions.
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Vote on the most important issues.
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Create a “Top 10” research priority list.
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How long does it take?
Most groups complete the process in about 12 to 18 months.
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Why is it important?
It makes sure that research focuses on real-life needs — not just what scientists think is important.