Preliminary study on Just-in-time intervention using wearable devices aimed at improving sleep / waking rhythm against mood disorder

Iwata Nakao0 个研究点目标入组 30 人开始时间: 2019年6月17日最近更新: 2023年10月17日

适应症

试验速览

暂无简介。

•1. Patients who have obtained their written consent by their own free will, after receiving sufficient explanation, to participate in this study
•2. Patients between 20 and 75 years of age at the time of obtaining consent (for undergraduates or adult adults)
•3. Mild to moderate depression, or outpatients diagnosed with mood disorders (major depressive disorder, bipolar disorder [types 1 and 2], dysthymia) based on DSM-5, or Also includes remission status
•4. In terms of medical interviews, the average sleep time on weekdays is less than 6 hours, or the actual arrival time is later than half the week, including weekends, that is later than the desired sleep time for the patient
•5. Any other treatment content (drugs etc.) currently in use
•6. I have a smartphone and am used to using it

•1. Patients with metal and rubber allergies when wearing devices
•2. Patients who are in the acute phase of depression and who the attending physician should center on intervention for mental symptoms
•3. Patients with obvious lupus
•4. Patients with psychophysiological insomnia (Patients who increase anxiety for sleep before sleep onset)
•5. Patients who can not agree not to browse mobile apps while driving
•6. Other patients judged to be inappropriate by the Principal Investigator or Investigator

发起方

Iwata Nakao