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May 6, 2020
 
Fitbit Charge 4
 
 

Fitbit announced this morning the launch of a new atrial fibrillation research study aiming to enroll hundreds of thousands of fitness-tracker and smartwatch owners.

Called the Fitbit Heart Study, it will passively and continuously monitor wearers' heart rates using the devices' photoplethysmography (PPG) sensors. A proprietary algorithm will interpret these readings and flag potential irregularities for follow-up: a free telehealth visit with a live doctor and, if needed, an ECG patch delivered through the mail to confirm the irregularity.

"The main goals are to see how well this model of healthcare – passive monitoring, virtual visits, comparing with a clinical diagnostic test – works for screening for atrial fibrillation," Tony Faranesh, a research scientist at Fitbit, told MobiHealthNews. "We're very excited for this study. We feel that our devices are really well suited for detecting a-fib, in that, because it's a disease that comes and goes, it's important that we have a long battery life ... and people don't have to take it off at night."

The Fitbit Heart Study is now recruiting U.S. adults aged 22 years or older who own any of Fitbit devices that support heart-rate tracking, a list that includes the Ionic, Inspire HR, Charge 3 and Charge 4 devices, as well as the full Versa family. The company says it will only share participants' data with study partners, and will immediately notify a user upon enrollment if a potential arrhythmia is detected within data logged up to 30 days prior to registration.

But seeing as most participants will likely never receive any of the system's arrhythmia notifications, Faranesh said that the company is hoping to enroll 200,000 to 250,000 of its device owners into the study so that its data analysis will satisfy regulators. Hitting these numbers will also help Fitbit better demonstrate that its approach won't yield too many false positives, added CTO and cofounder Eric Friedman.

"The regulatory community, while they want people who are sick to go to the hospital, they're also equally interested in [making sure] people who aren't sick don't go to the hospital," he told MobiHealthNews. "Because we're a consumer product, they want to make sure we have scope backing our proof that people won't overwhelm the medical system. That's part of the reason for the large size of this study."

And on the topic of Fitbit's regulatory efforts, the study announcement also came with a reaffirmation of the company's ongoing development of an on-board ECG feature for its devices. Friedman said that the company has wrapped up a pivotal trial and submitted the feature for approval from regulators, and stressed that ECG spot detection of atrial fibrillation and the Fitbit Heart Study's continuous PPG "guardian angel" approach are complementary efforts for round-the-clock health monitoring.

"ECG has a role, and we're working on ECG as well," he said. "But because we have a 24-hour product, we have the unique ability to understand what is happening in the human body holistically throughout the day.

"You can almost think of these working in parallel, where if you have an event and you're awake, we can alert you and say 'Hey, now might be a good time to take an ECG.' But that's not necessarily required, so these kind of work in tandem with each other instead of in opposition."

WHY IT MATTERS

Fitbit has clearly made its mark in fitness and general health over the years, which allows the company to establish an increasing presence among employer and insurer wellness plans. And while the company's devices have also played a role in some clinical studies as a continuous-activity or sleep-health monitor, the launch of Fitbit's first large-scale study to identify a cardiac disease is a major step toward broader clinical use.

"We've leveraged heart rate from just saying 'Hey, this is kind of cool. You can see your heart rate through the day,' to things like understanding sleep stages, understanding when your heart rate is elevated. And recently we released something called Active Zone Minutes, which uses your heart rate to figure out an appropriate-level workout for you," Friedman said. "We're really excited about moving on to this heart health stuff. It's really thinking about 'How do we be proactive in terms of helping people identify their condition?'"

The results of the Fitbit Heart Study will help the company's ongoing regulatory efforts, but will also serve as another test of whether a consumer-device-driven detection and virtual-care model is viable at scale – a particularly relevant subject considering the industry's recent swing toward telehealth.

"We considered very carefully whether the timing was right to launch this trial amidst the COVID-19 crisis," Faranesh said. "Atrial fibrillation is still an important problem. It's not going away, and the design of the trial is that people can enroll, onboard and just participate virtually. It doesn't require people to have any additional contact with people. ... We're not introducing any risk, and people are relying on telehealth even more during these times. It's a good test of this healthcare model going forward."

THE LARGER TREND

It's hard not to draw comparisons between Fitbit's latest effort and those of Apple, its chief competitor in the smartwatch space.

The latter company launched its Apple Heart Study in conjunction with Stanford Medicine back in 2017, and eventually recruited more than 400,000 participants to the research project, which also relied on a heart-rate sensor and accompanying algorithm to detect potential arrhythmia. Since then, Apple has announced a small handful of Watch-based studies focused on sound exposure, menstrual cycles, heart rate and physical activity.

Apple also made atrial fibrillation detection a focal point for consumer wearables since introducing on-board ECG to its Series 4 device in late 2018, with others like Withings following suit in the years to come. And while Fitbit does not directly offer the functionality on its devices, third-party app-makers like FibriCheck have developed their own FDA-cleared apps and algorithms for PPG-based arrhythmia detection for Fitbits and other smartwatches.

Still, it's not like Fitbit has slowed much in the roughly half-year since it signing the sale to Google. November came with an OS update sporting heart-rate and sleep-tracking features, while January saw the activation of blood-oxygen-level variability measurements for Sp02-enabled devices. The tail end of March also bore news of a new fitness tracker sporting GPS and heart-activity tracking.

 
nurochek system
 
 

This morning the FDA granted Australian company Headsafe a 510(k) clearance for its connected headgear that is able to perform an assessment of the brain. 

Named Nurocheck, the system uses Visual Evoked Potential (VEP) in order to gauge brain health. When a user puts on the headgear, which includes a set of goggles, the system presents visual stimulus to the brain. As this process is taking place, EEG sensors that are embedded in the device are able to record brain activity, according to the company. 

Finally, the data from that session is transmitted to a smartphone and then can be stored in the cloud. 

WHY IT MATTERS 

The new announcement means that the company can start to roll out its product to the U.S. market, thereby expanding its global footprint.

“Today’s announcement represents a historic milestone for our company, and we are eager to begin execution of our market launch in the United States,” said Dr. Adrian Cohen, CEO and founder of Headsafe. “In addition to our commercialization efforts in the U.S., we expect to accelerate our research activities to deepen the body of scientific evidence supporting the use of the Nurocheck system in the management of specific neurological conditions.”

THE LARGER TREND

This isn’t the first connected EEG on the market. Zeto is a Santa Clara, California-based startup that created a wireless headset, which uses dry electrodes, and proprietary software. Cleared by the FDA, the headset, called the zEEG, is able to perform an EEG reading and then transfer those results onto a provider’s laptop, phone or tablet via the cloud. 

In 2015, it was reported that the U.S. Department of Defense tapped BrainScope to put its FDA-cleared Ahead 200 device into action. The device consists of a headpiece with a number of EEG leads that connect to an Android smartphone, which runs the diagnostic software. 

 
 
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By HIMSS Insights
 
There is a renaissance of wearables in digital healthcare. More and more of them, many AI-empowered, are finding their way into serious clinical trials, thus contributing to medical evidence and ultimately better patient care. But with data comes responsibility: The question of how to design a digital healthcare data space that respects the privacy of individuals while at the same time providing maximal medical benefit is more important than ever.

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Now and in the weeks ahead, HIMSS20 Digital will be featuring an array of presentations that had been planned for the 2020 HIMSS Global Health Conference & Exhibition – enabling registrants to view them on demand. We'll also be showcasing stories that highlight technology's ongoing and essential role in combating the worldwide COVID-19 pandemic. This is a pivotal moment for professionals across the global health ecosystem. So check back here regularly for must-have insights about new technologies, trends, policies and other healthcare innovations.
 
 
 
 
 
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