Studies on how the use of devices affects human physiology
- Conditions
- ot applicable
- Registration Number
- JPRN-UMIN000050380
- Lead Sponsor
- Tohoku University
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 160
Not provided
Patients with the following clinically problematic diseases: Hematological diseases renal diseases endocrine disease Pulmonary disease Gastrointestinal disease Cardiovascular Diseases Liver disease Those with a history of, or currently suffering from, psychiatric or mental disorders Those with a history of serious head and spinal cord trauma, surgery, gastrointestinal tract, urinary tract bleeding, major surgery, or serious non-head trauma within the past 3 months Pregnant or lactating mothers. The Principal Investigator will confirm whether or not the above conditions apply to the applicant at the time of application by e-mail, etc., and at the time of explanation. If the applicant is not sure, the Principal Investigator will contact a licensed physician on the spot to determine whether or not the condition applies to the applicant and whether or not the applicant may participate. Other applicants who are deemed ineligible for inclusion by the Principal Investigator (e.g., those with extreme sleep disorders or excessive stress, those with symptoms such as menopausal disorders, etc.). Students and staff members affiliated with the principal investigator's or subinvestigator's laboratory, as well as students who are involved in grade approval by the principal investigator or subinvestigator, will not be eligible for inclusion in the study.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Changes in blood metabolites and soluble factors, gene expression changes in immune cells, and changes in biological signals (pre- and post-device use)
- Secondary Outcome Measures
Name Time Method