A study to evaluate the effect of intake of astaxanthin on the status of stress and sleep in adult.
- Conditions
- Healthy adult
- Registration Number
- JPRN-UMIN000033863
- Lead Sponsor
- JXTG Nippon Oil & energy Corporation
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete: follow-up complete
- Sex
- All
- Target Recruitment
- 60
Not provided
(1) Subjects who are 0mm as a result of VAS stress. (2) Subjects who routinely use food or medicine containing of astaxanthin. (3) Night and day shift worker or manual laborer. (4) Subjects with the smoking custom. (5) Bed time is after 2:00 (6) Subjects who drink much alcohol. (7) Subjects who dose not engage in the periodical labor. (8) Subjects who has got a rash with surgical tape, or may become infected with surgical tape, or that tape is easy to come off. (9) Subjects who have a disease on treatment or are judged to that medical treatment are necessary by the doctor. (10) Subjects who are under treatment or a history of sleep apnea syndrome or are strongly suspected of having sleep apnea syndrome. (11) Subjects diagnosed with chronic fatigue syndrome. (12) Subjects who have treated oral or dental care within the last one month prior to the current study or are planned to treat oral or dental care. (13) Subjects who have oral or dental problems with bleeding. (14) Subjects who were under treatment or have a history of serious diseases(e.g., diabetes, liver disease, kidney disease, or heart disease). (15) Subjects who are judged as unsuitable for the study based on the results of lifestyle questionnaire and other questionnaires. (16) Those who can not carry out the procedures of various tests to be carried out during this study. (17) Subjects having possibilities for emerging allergy related to the study. (18) Subjects who are judged as unsuitable for the study based on the results of clinical and physical examination on preliminary examination. (19) 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. (20) Subjects who are planned to become pregnant after informed consent for the current study or are pregnant or lactating. I omit (21) for input regulation
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Japanese version of POMS2
- Secondary Outcome Measures
Name Time Method