Patient trust in the trial or the medication can affect recruitment and result in either nonadherence or early drop-out causing potential delay to clinical trial completion and reduced data quality. These impacts can have a significant knock-on effect on overall costs, launch success and sales revenue.
We help you detect behavioural risk early, enabling Clinical Researchers to reliably predict which patients are at risk of nonadherence. Our tools categorise patients by level of risk, helping you understand why a patient is at risk and inform the development of evidence-based mitigating interventions.
TARA™ (Treatment Activation and Adherence Risk Assessment)
Predicting and mitigating nonadherence in clinical trials and patient support programmes
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