A clinical study to evaluate the efficacy of body fat reduction by continuous ingestion of test food and exercise. ( SME-2021-02-FOSHUS)

A clinical study to evaluate the efficacy of body fat reduction by continuous ingestion of test food and exercise. ( SME-2021-02-FOSHUS) - A clinical study to evaluate the efficacy of body fat reduction by continuous ingestion of test food and exercise.

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

JPRN

Registry ID

JPRN-UMIN000044866

Enrollment

148

Registered

2021-07-25

Start date

2021-07-26

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

None listed

Interventions

Daily intake of test food and exercise for 12 weeks Daily intake of control food and exercise for 12 weeks

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: (1) Males and females who are -> 20 years old at the time of IC acquisition and <65 years old at the end of the study. (2) Subject, 25 kg/m2 <- BMI < 30 kg/m2. (3) Those who can visit to destination medical institution on the scheduled date. (4) Those who have submitted written informed consent after fully understanding the purpose and content of this study.

Exclusion criteria

Exclusion criteria: (1) Those who have regular hard exercise. (2) Those who heavy use of alcohol or smoke. (3) Those who continuously ingest foods for specified health use, foods with functional claims, health foods, and foods that may affect body fat evaluation. (4) Those who continuously take medicines. (5) Those who are participating in other study or planning to participate or participated within the past 4 weeks. (6) Those who are: a) heart, liver, or kidney disease (including complications of other diseases) b) having a history of cardiovascular disease c) diabetes d) allergic to test foods e) having a respiratory illness (7) Others who are judged inappropriate for participant by the investigator.

Design outcomes

Primary

Measure	Time frame
Abdominal total fat area	—

Countries

Japan

Contacts

Public ContactKeisuke Yasumoto

Suntory Holdings Limited Research Strategy Planning Department

Keisuke_Yasumoto@suntory.co.jp03-3182-0496

Outcome results