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Effect of edible powder ingestion on postprandial blood parameters.

Effect of edible powder ingestion on Cognitive function and hormones. - Effect of edible powder ingestion on postprandial blood parameters.

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000037516
Enrollment
20
Registered
2019-07-31
Start date
2019-08-01
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

Healthy adults

Interventions

test diet consumption Test diet consumption &gt
Control diet consumption

Sponsors

TES Holdings Co., Ltd.
Lead Sponsor

Eligibility

Sex/Gender
Male

Inclusion criteria

Inclusion criteria: (1)Age>=50 and <=69years (2)Day workers (3)Subjects who sleep at least five hours per day usually (4)Subjects who can take a test using personal computer (5)Subjects who have given written informed consent prior to start of study

Exclusion criteria

Exclusion criteria: (1)Subjects who have a history or signs of a neurodegenerative disorder or cerebrovascular disease or cardiovascular disease or thyroid disease (2)Subjects having a liver, kidney or respiratory disease, endocrine disorder, metabolic disorder, organ disorder, autoimmune disease, allergy disease, mental disorder, cancer, diabetes, infection disease, or other diseases (3)Subjects who take a sleeping drug, antipsychotic drug, anti-anxiety drug, antidepressant, antidiabetic drug or antihyperlipidemic drug (4)BMI>=30 (5)Subjects who usually take a functional foods or supplements that affects results (6)Heavy drinker (7)Subjects who have donated over 200 mL of blood within the last one month prior to the current study or over 400 mL of blood within the last three months prior to the study (8)Subjects who have severe anemia (Hb <=7g/dL) (9)Subjects who have been to get sick by collecting venous blood (10)Subjects who have allergic reaction to control or test food (11)Subjects who can't eat served control or test food all (12)Subjects who are planned to participate in other clinical study during current study (13) Subjects who can't keep eating and exercise habits during study (14)Subjects who are judged to be inappropriate for the study by the medical doctor or investigator for other reason

Design outcomes

Primary

MeasureTime frame
Blood parameters at 60, 120, and 240 min after single ingestion of edible powder containing diets or control diet.

Secondary

MeasureTime frame
Cognitive function, subjective assessment, etc., after single ingestion of edible powder containing diets or control diet.

Countries

Japan

Contacts

Public ContactTamura Toshiyasu

TES Holdings Co. Ltd Department of Development for Clinical Trials

t.tamura@tes-h.co.jp03-6801-8480

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026