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Evalution of the effect of whey protein hydrolysate on feeling-related indices by single intake

Not Applicable
Conditions
Healthy adult males and females
Registration Number
JPRN-UMIN000053807
Lead Sponsor
APO PLUS STATION CO., LTD.
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete: follow-up continuing
Sex
All
Target Recruitment
96
Inclusion Criteria

Not provided

Exclusion Criteria

1)Those who consume pharmaceuticals, quasi-drugs, foods for health maintenance and recovery, and are unable to discontinue such consumption during the study period 2)Those who currently consume foods and drinks for the autonomic nervous system, sleep, metabolism, and intestinal environment, and are unable to discontinue such consumption during the study period 3)Those who have participated in studies including the ingestion of other foods or the use of cosmetics and pharmaceuticals within 1 month before the consent obtained, or who will participate in other studies during the study period 4)Heavy drinkers of alcohol 5)Those with irregular rhythm of daily life 6)Those who are habitual smokers 7)Those who plan to make major changes in their lifestyle during the study period 8)Those who have had a life event within 1 month that has affected them physically or mentally 9)Those who daily consume large amounts of milk, dairy products, or dairy-derived protein foods 10)Those who currently visit hospital and are on treatment for any disease 11)Those who have had surgery on the gastrointestinal tract (other than appendicitis surgery) 12)Those who are judged by the principal investigator or sub-investigator to have a disease associated with physical or mental disorder 13)Those who score 21 or higher on BDI-II 14)Those who are at risk of suicide on the 9th question of the BDI-II 15)Those with serious liver, kidney, heart, respiratory, endocrine, metabolic, psychiatric, or higher brain dysfunction 16)Those who have previously experienced feeling fainted, deterioration of physical condition, or vasovagal reflexes at the time of blood sampling 17)Those who may be allergic to milk or soy, or have lactose intolerant 18)Those with a current or history of allergy to drugs or foods 19)Those who are currently pregnant or lactating, and who wish to become pregnant during the study period 20)Those who are judged as ineligible for the study by the principal investigator

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Secondary Outcome Measures
NameTimeMethod
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