A study for evaluating the effect of sleep and fatigue using the air conditioner

Not Applicable

• Conditions: Healthy adult

• Registration Number: JPRN-UMIN000028063
• Lead Sponsor: TTC Co.,Ltd.

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Start: 2017-07-04
• Last Update Posted: 17 October 2023

Recruitment & Eligibility

• Status: Complete: follow-up complete
• Sex: All
• Target Recruitment: 12

Inclusion Criteria

Not provided

Exclusion Criteria

1) Subjects who routinely use test device 2) Subjects who perform an act for the improvement of the quality of the sleep, the stress, and fatigue 3) Subjects who routinely intake foods that possibly affect sleep, stress, and fatigue 4) Subjects who are unsuitable for the sleep in the group 5) Subjects who needs aromatherapy etc. at bedtime 6) Subjects who wake after sleep onset for nocturia more than twice a week 7) Subjects who drink more than once a week 8) Subjects who smoke 9) Night and day shift worker or manual laborer 10) Subjects who have a disease under treatment or are judged to that medical treatment are necessary by the doctor 11) Subjects who have under treatment or a history of sleep apnea syndrome or is strongly suspected of sleep apnea syndrome 12) Subjects who have had a diagnosis of chronic fatigue syndrome 13) Subjects who have under treatment or a history of serious disease (e.g., diabetes, liver disease, kidney disease, or heart disease) and disease to affect the adrenal cortical hormone secretion 14) Subjects who have any discomfort in the wrist or arm 15) Subjects who are judged as unsuitable for the study based on the results of lifestyle questionnaire and other questionnaires 16) Subjects who are judged as unsuitable for the study based on the results of clinical and physical examination on preliminary examination 17) Subjects who have participated in other clinical study within the last one month prior to the current study or are planned to participate in other clinical study after informed consent for the current study 18) Subjects who intend to become pregnant or lactating 19) Subjects judged as unsuitable for the current study by the investigator

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
chida-Kraepelin test

Secondary Outcome Measures

Name	Time	Method
Purdue Pegboard Test, OSA sleep inventory MA version, Quality of life assessment, Fatigue VAS, Concentration VAS