The USFDA has approved a new device called Nightware to reduce sleep disturbances in adults aged 22 years or older. This device is intended to reduce sleep disturbances in people with nightmare disorder or those who have nightmares due to Post Traumatic Stress Disorder (PTSD). People suffering from nightmares do not get enough sleep, and Nightware is a low-risk therapy option that utilizes digital-technology to provide temporary relief in such patients. The device analyzes the heart rate and motion during sleep and provides gentle vibrations through touch.

Nightware will be available as a prescription device for home use. The device will use an Apple watch and an iPhone to monitor body movements and heart rate during sleep. A proprietary algorithm will send this data to the Nightware server, analyzing and creating a unique sleep profile for the patient. The device should not be used as…