Exploratory Study on the Effects of Food Ingredient Intake on Daily Physical Complaints -Placebo-Controlled, Double Blind Crossover Study-

Exploratory Study on the Effects of Food Ingredient Intake on Daily Physical Complaints -Placebo-Controlled, Double Blind Crossover Study- - Exploratory Study on the Effects of Food Ingredient Intake on Daily Physical Complaints -Placebo-Controlled, Double Blind Crossover Study-

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

JPRN

Registry ID

JPRN-UMIN000056868

Enrollment

Registered

2025-01-30

Start date

2025-01-31

Completion date

Unknown

Last updated

2026-06-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

None listed

Interventions

After consuming the test food once, a washout period will follow, and the control food will be consumed once. After consuming the control food once, a washout period will follow, and the test food wil

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: (1) Healthy males and females in the age between 30 and 64 years (2) Subjects who can have explanations and examinations in a remote environment (web conference system, web questionnaire, etc.) (3) Subjects who can come to the designated examination facility on the scheduled visit date (4) Subjects who can submit the written informed consent form

Exclusion criteria

Exclusion criteria: (1) Subjects who regularly consume pharmaceuticals or quasi-drugs that may affect the efficacy evaluation of the test food (2) Subjects who continuously consume food for specified health use, functional foods, or health foods that may affect the efficacy evaluation of the test food (3) Subjects whose lifestyle is scheduled to change drastically before or after the start of the study (including business trip, travel, etc. that will significantly change the rhythm of their daily life) (4) Subjects who are currently participating in other studies, who have participated in other studies within 4 weeks after their completion, or who are planning to participate in other studies during the study period (except for the specific studies). (5) Other subjects who are judged by the investigator as unsuitable for the study

Design outcomes

Primary

Measure	Time frame
Questionnaire on daily physical complaints	—

Countries

Japan

Contacts

Public ContactRyoko Koizumi

Apoplus Station Co., Ltd. CRO Department Clinical Operations Division

food-contact@apoplus.co.jp03-6777-7789

Outcome results