Development of technology for the quantification of stress and well-being using pulse, voice, and electrodermal data: A pilot study
Not Applicable
- Conditions
- Healthy volunteers
- Registration Number
- JPRN-UMIN000034725
- Lead Sponsor
- Keio University School of Medicine
- Brief Summary
under analysis
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete: follow-up continuing
- Sex
- All
- Target Recruitment
- 28
Inclusion Criteria
Not provided
Exclusion Criteria
(1) Those who are under treatment for psychiatric diseases such as depression. (2) Those who have a disease which may affect acquisition of physical data (eg. facial palsy, limb palsy, involuntary movement, cardiovascular diseases, difficulty speaking, etc.). (3) Those who have difficulties in operating personal computers such as sending and receiving e-mails, entering information on websites. (4) Those who have difficulties obtaining physical data for any work-related reason. (5) Those who are considered to be ineligible by the PI or investigators.
Study & Design
- Study Type
- Observational
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method To see if data collection is feasible under the protocols and to identify any problems that arise during the course of the study.
- Secondary Outcome Measures
Name Time Method 1. Retention rate of using sensing device and wearable device 2. Change in vital data along with any environmental changes/activities