A new iPhone app called mPower is giving scientists more insight than ever into the capacities and challenges of people living with Parkinson’s. Nonprofit Sage Bionetworks is a biomedical research organization that collected an unparalleled amount of data through its mPower app, which included a dataset comprised of the daily experiences of more than 9,500 Parkinson’s sufferers. This dataset offers more valuable information than any other study on Parkinson’s has provided, as it takes into consideration millions of data points that were collected on an almost continuous basis through the mhealth (mPower) platform.
Sage Bionetworks says that its researchers, through the use of the mobile technology marvel mPower, have received an unprecedented look into the activities and day-to-day changes that Parkinson’s sufferers experience as they deal with their condition.
In the past, Parkinson’s researchers typically relied on small-group studies and data, which included participants in only about the 100-person range. With mPower, scientists are able to view and study data on a larger scale, and the scope of the research is giving more clues as to how Parkinson’s sufferers deal with challenges and treatment pertaining to speech, dexterity, memory, gait, and balance.
How Does mPower Collect Data?
The mPower app collects data on the abilities or disabilities of Parkinson’s sufferers in a variety of ways, all with the intent of helping the estimated seven-plus million people living with the disease improve speech, put an end to tremors, strengthen memory, and help other degenerative conditions.
The app evaluates dexterity by asking users to do a speed-tapping exercise, which the iPhone’s touchscreen turns into data for researchers. To measure speech ability, users talk into their iPhone’s microphone and record their pronunciation of vowels (and other difficult parts of speech) for 10 seconds. They also use mPower to track their medication intake and to see if abilities improve after taking the drugs.
The mPower app gathers data, and scientists and doctors use it to research Parkinson’s on an ongoing basis. Participants using the app are able to control who sees their data, and intended data researchers include mPower-affiliated doctors and scientists, as well as specified researchers worldwide.
The data collected has already helped researchers view symptom variations that could assist them in intervening in ways never before considered. The mPower app, along with additional text messaging health services that encourage people to stay in communication with doctors regarding their health, has the potential to offer big breakthroughs in Parkinson’s treatment and the treatment of other diseases.