Clinical Trials and Cancer Research
Additional presentations may examine decentralised and hybrid trial designs, electronic consent, remote monitoring, and wearable-derived endpoints. Researchers will discuss digital biomarkers, patient-reported outcome measures, and pragmatic trials embedded in routine care. Sessions may cover adaptive and Bayesian designs, master protocols, and platform trials that test several interventions simultaneously. Attention will be given to recruiting underrepresented groups, including older women, pregnant patients, rural populations, and those with limited literacy. Data monitoring committees, good clinical practice, regulatory pathways, and transparent reporting will be reviewed. Registries, electronic health records, qualitative and mixed-methods research, and patient and public involvement will also feature. Building research capacity in low-resource settings and sharing data responsibly will be encouraged.
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