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Effect of Ingestion of the Test Food A and Test Food B on Body Composition: An Exploratory Study

Effect of Ingestion of the Test Food A and Test Food B on Body Composition: An Exploratory Study - Effect of Ingestion of the Test Food A and Test Food B on Body Composition: An Exploratory Study

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000054576
Enrollment
240
Registered
2024-06-06
Start date
2024-06-07
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 adult

Interventions

Non-ingestion Daily ingestion of test food A for 16 weeks. Daily ingestion of test food A and test food B for 16 weeks.

Sponsors

Hokkaido Information University
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Subjects who fully understand significance, content and purpose of this study and who agree to participate in this study with a written informed consent. 2. Subjects who can write diary and questionnaire, visit an inspection facility and receive examinations in designated days.

Exclusion criteria

Exclusion criteria: 1. Subjects who cannot perform activities of daily living on their own. 2. Subjects who cannot walk on their own and are restricted daily activities by physicians. 3. Subjects who are under physician's advice, treatment, and/or medication for quadriplegia, depression, dementia, neurological disease, amyotrophic lateral sclerosis. 4. Subjects with implantable electronic medical devices. 5. Subjects who are under treatment or have a history of serious diseases, or who affected with infectious diseases requiring reports to the authorities. 6. Subjects with major surgical history relevant to the digestive system. 7. Subjects who cannot ingestion test foods due to any reason, such as allergy. 8. Subjects who regularly take foods similar to test food A. 9. Subjects who regularly take foods similar to test food B. 10. Heavy smokers, alcohol addicts or subjects with disordered lifestyle. 11. Subjects who donated either 400 ml whole blood within 16 wks (women), 12 wks (men), 200 ml whole blood within 4 wks, or blood components within 2 wks, prior to this study. 12. Subjects who currently participate in other clinical trials or participated within the last 4 wks prior to the current study. 13. Subjects who are ineligible due to physician's judgment.

Design outcomes

Primary

MeasureTime frame
Body composition (body weight, body fat rate, body mass index, muscle mass, lean body mass, Skeletal Muscle Mass, SMI, ECW/TBW) at 16 weeks after ingestion.

Secondary

MeasureTime frame
Physical fitness test, Vital signs, Blood inflammatory marker, Blood anti-oxidant markers, Blood lipids, Blood glucose, Questionnaire assessed frailty.

Countries

Japan

Contacts

Public ContactNaoyuki HONMA

Hokkaido Information University Health Information Science Center

hisc-acad.res@s.do-johodai.ac.jp011-385-4430

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Aug 5, 2026