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Play, download and edit the free video Making Decentralized Trials Common Place for Rare Diseases Patients.

Decentralized clinical trials have proven to allow continued recruitment and retention of patients, keeping trials and patient’s wellbeing on track, but what about keeping daily life on track for a patient and their family?

For rare disease patients, a clinical trial may be the important next step in their healthcare journey, an important key that unlocks the next door of treatment, so it’s imperative for those trial schedules to be flexible and meet the life needs of the patient. We know that a patient is more than their health condition — they’re parents, children, they go to school and work, they have a life outside of clinical research, and trial designs don’t always consider that.

MRN has spent close to two decades advocating for a decentralized, patient-focused approach to clinical trials, bringing trial visits to the patient in their own community. While the industry in recent years has discussed various decentralized, patient-centric strategies, COVID-19 brought their implementation to the very forefront of clinical trial development. As an industry, we saw sites close and studies lose their trial patients. Because of this, eyes have been opened to all of the possibilities decentralized solutions can bring to a trial, but with implementation comes a learning curve.

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