By Deborah Kilpatrick, Ph.D. Murali Doraiswamy, M.D.
Chief Executive Officer Professor of Psychiatry and Medicine
Evidation Health Duke University Health System
Given the widespread adoption of mobile technologies and digital health apps by patients, we now have a view into the continuous patient journey like never before. We can now “quantify real life” of patients and measure health outcomes beyond traditional clinical trials, at scale. And in this digital era of medicine, we have more robust analytical tools that can sift through massive, complex datasets faster and more reliably. Whether it is in Type 2 diabetes or multiple sclerosis or heart failure, the ability to quantify outcomes from real life patient data is going to change the way we think about the volume-to-value transformation.
Therapeutics industry leaders can now address some direct drivers of the historical gap between trial efficacy and post-launch effectiveness with solutions that enable:
- Access to broader connected populations
- Collection of novel real life data from patients
- Quantification of real life outcomes
1. Access to Connected Populations
Clinical development strategies for drugs and devices include fundamentals ranging from recruiting eligible patients to capturing data at various points in time according to a pre-specified protocol. None of these steps go away in the digital era, but the tactics for getting them done are undergoing truly revolutionary change.,
Digital technologies provide new channels for accessing target patient populations. In connecting with patients outside of traditional clinical settings, we are able to recruit patients for studies much faster, discover patterns across segments, and support patients in their everyday lives.
Equally important, the benefits are not limited to the number of patients recruited or the improved efficiencies of the process. Digital technologies fundamentally expand the datasets we can use to quantify outcomes in the real world. That means we can more accurately correlate outcomes with patients’ daily lives and behaviors.
2. Collection of Novel Real Life Data
The most important expansion of our clinical development data universe is arguably our new ability to continuously and passively measure patient behaviors upon informed consent. For example, tracking sleep, physical activity, social media activity, and wireless sensor data all enhance the context available for analysis.
In the near term, this new information can shed light on the efficacy-effectiveness gap between phase III trial results and what happens in post-launch settings. When combined with medical information including EHRs, claims data, and genomics, this new understanding of how patient behaviors drive health outcomes creates a direct path to precision medicine solutions.
3. Quantification of Real Life Outcomes
Gathering novel data from more people, more efficiently, is only helpful if it leads to scientifically valid conclusions that prove outcomes. We have always known that patient behaviors directly influence symptomology and disease progression/regression in many therapeutic areas, but quantifying the impact has traditionally been an elusive goal. That has changed.
Therapeutic areas that are benefiting most from this new approach are those where patient behaviors outside the clinic walls disproportionately impact health outcomes. In our experience to date, the use cases for quantifying how real life patient behaviors drive health outcomes are now quite broad and accessible. For example:
- Segmenting populations by behaviors: identifying super-responders and non-responders to a medication adherence mobile app in cardiometabolic disease
- Evaluating "Services around the Pill": optimizing digital health interventions to impact vaccination patterns and reduce infection rates during flu season
- Characterizing real life quality of life improvement: measuring data reflecting productivity and daily symptom improvement in depression and anxiety
- Identifying new digital biomarkers for disease status based on quantified behaviors: establishing links between daily activity patterns and flares in multiple sclerosis
Connecting with patient populations, collecting continuous behavioral data, and quantifying health outcomes on large behavior datasets all benefit from digital tools -- but the greatest benefit is realized when the three tactics are combined.
For example, a top global pharma company worked with Evidation Health with the goal of improving patient adherence to medication and lifestyle modification in the diabetes market. The project started by connecting with 300,000 patients and segmenting that population into clusters. The platform collected real life behavioral data across well over 6 months of observation and linked relevant behavioral activity (diet, sleep, etc.) to medical adherence.
Ultimately, this enabled a top global pharma company to quantify health outcomes and leverage behavior-driven insights for dynamic intervention targeting.
We might not have imagined a decade ago that we’d be here so quickly. But suddenly we find ourselves able to quantify health outcomes like never before, in settings we never imagined, in populations we might not have ever reached—in their real lives. This is indeed an idea whose time has come.
To learn more about how healthcare companies are using Evidation Health’s Real Life Study Solution to quantify health outcomes in the digital era of medicine, follow @evidation.
PMD is a scientific advisor to Evidation Health and has served as an advisor to leading businesses, advocacy groups and government agencies.
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Deborah Kilpatrick is the Chief Executive Officer of Evidation Health. Prior to this role, she served as the Chief Commercial Officer of genomic diagnostics company CardioDx. Earlier in her career, Deborah held multiple leadership roles at Guidant Corporation, including Research Fellow, Director of R&D, and Director of New Ventures in the Vascular Intervention Division. She serves on the Georgia Tech Advisory Board and is a Fellow of the American Institute of Medical and Biological Engineering. Deborah is a co-founder of the MedtechVision Conference, now held annually in Silicon Valley and has received many awards including 100 Women of Influence in Silicon Valley. She holds BS, MS and PhD degrees in mechanical engineering with a bioengineering focus from Georgia Tech.
Murali Doraiswamy is a scientific advisor to Evidation Health and has served as an advisor to leading businesses, advocacy groups and government agencies. Doraiswamy is a leading physician scientist in the areas of brain health and personalized medicine at Duke Medicine where he is a Professor in the Division of Translational Neuroscience and Director of the Neurocognitive Disorders Program in Psychiatry. He also serves as a member of the Duke Institute for Brain Sciences and the Duke Center for Personalized Medicine. Doraiswamy has served as an advisor to leading government agencies, advocacy groups and businesses, and received many awards including a special Congressional recognition. He is the coauthor of a popular book, The Alzheimer's Action Plan.