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An advocacy colleague of mine just complained about having had to sit through a talk short of an hour on how to talk patients into participating in clinical trials *without* a single reference to what clinical trials have to deliver for patients, so here some explaining 🧵
relevant for any patient considering participating in a clinical trial and equally, any patient advocate asked to provide 'a patient perspective' on clinical trials
in cancer, considering ignoring if it's a trial where the risk to yourself and your life is negligeable or you don't dare contradicting your oncologist anyway (though consider changing oncologist in that case)
