Clinical Evaluation of the Effects of Dietary Sulforaphane on Sleep in Healthy Volunteers
Not Applicable
- Conditions
- Healthy adults
- Registration Number
- JPRN-UMIN000029141
- Lead Sponsor
- Tokai University School of Medicine
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete: follow-up complete
- Sex
- All
- Target Recruitment
- 15
Inclusion Criteria
Not provided
Exclusion Criteria
1) Subjects with heart disease, kidney disease, diabetes and other serious disease 2) Subjects who had serious disease and judge not to be suitable for this study 3) Subjects with risk of allergy regarding to this study 4) Subjects who have irregular life style 5) Subjects who cannot stop the use of medicines, herbal medicines and health foods which may affect sleep quality 6) Subjects who cannot take interventional foods following instructions and write life diary 7) Subjects who are in other clinical trials, or participated in other clinical trials within 2 months 8) Subjects who are judged unsuitable for this study by principal investigator and doctors
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Sleep questionnaire(Oguri-Shirakawa-Azumi sleep questionnaire, The St. Mary's Hospital sleep questionnaire, VAS) before and 1, 2, 4 weeks after the intervention with "sulforaphane" or placebo.
- Secondary Outcome Measures
Name Time Method Sleep monitoring by wearable devices, Autonomic nervous function tests, Salivary markers(Humoral factor), Physical parameters