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A study for evaluating psychological and physical effect of intake food at commuting time. A no treatment-controlled, stratified randomization, single-blind, parallel trial.

A study for evaluating psychological and physical effect of intake food at commuting time. A no treatment-controlled, stratified randomization, single-blind, parallel trial. - A study for evaluating psychological and physical effect of intake food at commuting time.

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000030895
Enrollment
100
Registered
2018-01-19
Start date
2018-01-26
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

Ingestion of test food at commuting (8 weeks (work day) ingestion) No intake at commuting time (8 weeks (work day))

Sponsors

Lotte Co., Ltd.
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: (1) Healthy males and females from 20 to 59 years of age (2) Subjects giving written informed consent

Exclusion criteria

Exclusion criteria: (1) Individuals who have symptoms that affect test food intake and walking (2) Currently, individuals are receiving treatment some diseases, especially mental health. Or individuals are using supplements or health foods for stress (3) Individuals presenting known food allergy in connection with the exam (4) Individuals who are pregnant (5) Individuals currently losing weight (6) Individuals who feel that it is difficult to keep eating test foods during commuting time (7) Individuals who think are not able to perform the test more than 80% on work day. (8) Individuals who are judged as unsuitable for the study by the investigator

Design outcomes

Primary

MeasureTime frame
Subject's body fat, before test, after 4 and 8 weeks from starting test

Secondary

MeasureTime frame
BMI, Body height, body weight, muscle mass, basal metabolic rate and abdominal girth of the subject, 4 and 8 weeks from starting test Subject's stress felt at attendance time (any day)

Countries

Japan

Contacts

Public ContactSusumu Kanno

Lotte Co., Ltd. Central Laboratory

Kanno_susumu@lotte.co.jp048-837-0187

Outcome results

None listed

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