Your browser doesn't support javascript.
loading
Daily Self-Monitoring and Feedback of Circadian Rhythm Measures in Major Depression and Bipolar Disorder Using Wearable Devices and Smartphones-The Circadian Rhythm for Mood (CRM®) Trial Protocol: A Randomized Sham Controlled Double-Blind Trial.
Yeom, Ji Won; Yoon, Yeaseul; Seo, Ju Yeon; Cho, Chul-Hyun; Lee, Taek; Lee, Jung-Been; Jeon, Sehyun; Kim, Leen; Lee, Heon-Jeong.
Affiliation
  • Yeom JW; Department of Psychiatry, Korea University College of Medicine, Seoul, Republic of Korea.
  • Yoon Y; Chronobiology Institute, Korea University, Seoul, Republic of Korea.
  • Seo JY; Department of Psychiatry, Korea University College of Medicine, Seoul, Republic of Korea.
  • Cho CH; Chronobiology Institute, Korea University, Seoul, Republic of Korea.
  • Lee T; Department of Psychiatry, Korea University College of Medicine, Seoul, Republic of Korea.
  • Lee JB; Chronobiology Institute, Korea University, Seoul, Republic of Korea.
  • Jeon S; Department of Psychiatry, Korea University College of Medicine, Seoul, Republic of Korea.
  • Kim L; Chronobiology Institute, Korea University, Seoul, Republic of Korea.
  • Lee HJ; Division of Computer Science and Engineering, College of Software and Convergence, Sun Moon University, Asan, Republic of Korea.
Psychiatry Investig ; 21(8): 918-924, 2024 Aug.
Article in En | MEDLINE | ID: mdl-39086163
ABSTRACT
The circadian rhythm for mood (CRM) is a digital therapeutic, which aims to prevent mood episode and improve clinical course in patients with major mood disorders. Developed on the circadian rhythm hypothesis of mood disorder, CRM predicts the impending risk of mood episode with its built-in algorithm, utilizing wearable devices data and daily self-reports, and provides personalized feedback. In a pilot study of the CRM, the users experienced less frequent and shorter duration of mood episodes than the non-users. To investigate the efficacy of the upgraded CRM, a double-blind, randomized, sham-controlled, parallel-group trial is designed. Patients aged between 19 and 70, diagnosed with bipolar I disorder, bipolar II disorder, or major depressive disorder, in a euthymic state for more than two months, can participate. During this 12-month trial, participants are assessed for episode recurrence every three months, and the efficacy of the CRM as a potential digital therapeutic is evaluated. Trial registration ClinicalTrials.gov Identifier NCT05400785.
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Psychiatry Investig Year: 2024 Document type: Article Country of publication:

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Psychiatry Investig Year: 2024 Document type: Article Country of publication: