Heavy Drinking Habits -induced cognitive decline
Conditions
Interventions
None listed
Sponsors
IMEQRD Co. Ltd.
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: 1. Japanese men and women in their 20s at the time of written consent 2. AUDIT score of 15 or higher, or non-drinkers with an AUDIT score of 0 3. Received sufficient explanation of the study's purpose and content, demonstrated capacity to consent, voluntarily agreed to participate, and provided written consent
Exclusion criteria
Exclusion criteria: 1. Currently receiving medication or outpatient treatment for any serious illness (as-needed medication permitted) 2. Currently receiving treatment for, or with a history of, psychiatric disorders (e.g., depression) or sleep disorders 3. Blood donation of more than 200 mL within 1 month or more than 400 mL within 3 months prior to consent 4. History of feeling unwell or experiencing vasovagal reflex during blood collection 5. Difficulty in self-collecting nasal samples using a swab 6. Difficulty complying with survey questionnaire requirements 7. Currently participating in another clinical trial or planning to do so during the study period 8. Deemed unsuitable as a participant by the principal investigator for any other reason
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Gene expression levels | — |
Secondary
| Measure | Time frame |
|---|---|
| -Blood biochemical tests -AUDIT -Smoking history -Exercise habits -Anxiety and depression symptoms (K6) -Sleep status (PSQI) -Correlation between primary and secondary outcomes | — |
Countries
Japan
Contacts
Public ContactYoshitada Hira
IMEQRD Co., Ltd. Planning and Sales Department
Outcome results
None listed