Hypertension, arteriosclerosis, sleep disorders
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: (1) Those who can adjust the measurement schedule (2) Those who can follow the precautions for participation in the experiment (3) Those who have no smoking habit. (4) Those who have not been diagnosed with any abnormality in blood test, urine test, chest X-ray, electrocardiogram, etc. at the medical checkup within one year
Exclusion criteria
Exclusion criteria: (1) If the subject has serious physical symptoms that make it difficult to cooperate in the research. (2) The subject is using an implantable medical device such as a pacemaker. (3) Those who cannot be confirmed to be normal after undergoing a medical examination that lacks items such as blood test, urine test, chest X-ray, and electrocardiogram in the medical examination described in the participation criteria (4), or those who have not undergone a medical examination. (4) Other cases in which the physician judges that participation in the survey is inappropriate.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Stage 1 (pre-workcation; 3 days) Explanation of the study, consent form, questionnaire, measurement of height, weight, body fat percentage, body mass index (BMI: body mass index indicating the degree of obesity), muscle mass, arterial stiffness, blood pressure, heart rate, autonomic nervous system function, physical activity, and sleep quality and duration. Stage 2 (workcation period; 5 days) Measures arterial stiffness, blood pressure, heart rate, autonomic function, physical activity, and sleep quality and duration. Stage 3 (post-workcation; 3 days) Questionnaire, weight, body fat percentage, BMI, muscle mass, arterial stiffness, blood pressure, heart rate, autonomic function, physical activity, and sleep quality and duration will be measured. | — |
Countries
Japan
Contacts
Teikyo University of Science Faculty of Life & Environmental Sciences, Center for Fundamental Education