Healthy subjects
Conditions
Interventions
Online evaluation environment: Answering questionnaires in a non-supervised environment such as at home.
Face-to-face evaluation environment: Answering questionnaires under supervision at a designated
Sponsors
Macromill, Inc.
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: (1) Men and women aged 30 to 59 years at the time of providing informed consent. (2) Individuals who feel a certain amount of stress in their daily lives. (3) Individuals who have received a full explanation of the purpose and content of the study, have the capacity to provide consent, can understand the content well, and provide their own consent via electronic informed consent.
Exclusion criteria
Exclusion criteria: (1) Individuals receiving medical treatment, medication, or counseling by a physician for psychiatric disorders such as depression, anxiety, insomnia, or panic disorder. (2) Individuals currently receiving medical treatment or medication by a physician for a serious chronic disease. (3) Individuals with a serious medical history of cerebrovascular, cardiac, hepatic, renal, hematologic, or endocrine disease. (4) Heavy drinkers. (5) Individuals who do not have a communication/private room environment at home where they can quietly respond to questionnaires. (6) Individuals with extremely irregular sleeping or eating habits. (7) Individuals whose living environment, dietary habits, or exercise habits may change significantly during the study period. (8) Women who are pregnant, may be pregnant, or intend to become pregnant during the study period.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Subjective mood and psychological state questionnaires | — |
Secondary
| Measure | Time frame |
|---|---|
| (1) Personality and psychological characteristics questionnaires (2) literacy questionnaire | — |
Countries
Japan
Contacts
Public ContactAnna Kadodani
Macromill, Inc. Clinical Trial Department, Life Science Division
Outcome results
None listed