Exploratory study of individual differences in the weight loss effect of exercise intervention on obese people [Trial No. g2022005]

Not Applicable

• Conditions: Healthy adults

• Registration Number: JPRN-UMIN000048462
• Lead Sponsor: Macromill,Inc.

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Start: 2022-07-26
• Study Completion: 2022-12-31
• Last Update Posted: 17 October 2023

Recruitment & Eligibility

• Status: Pending
• Sex: Male
• Target Recruitment: 60

Inclusion Criteria

Not provided

Exclusion Criteria

(1) Subjects currently receiving drug treatment due to some chronic disease. (2) Subjects who have a history or current history of diseases such as liver disease, renal disease, respiratory disease, endocrine disorder, metabolic disorder, organ disorder, gout, rheumatism, autoimmune disease, mental disease, cancer, infectious disease, and arrhythmia. (3) Alcoholic drinkers. (4) Subjects with a history of gastrointestinal resection. (5) Subjects who collected 200 mL of blood within 1 month or 400 mL or more within 3 months of the start of this study. (6) Subjects who have skin diseases (atopic dermatitis, acne vulgaris, psoriasis, etc.) on face. (7) Subjects who use medical external medicine on the face. (8) Subjects who have excessive sunburn on the face. (9) Subjects who have skin diseases, metal allergies, pacemakers, etc. in their bodies. (10) Subjects who plan to participate in other clinical trials during the trial participation period. (11) Subjects who are not day shifts such as night shifts and rotation shifts (12) Subjects who have felt sick at the time of blood collection, or those who have difficulty in collecting blood because the blood vessels in the arm are difficult to see. (13) Subjects who have a history of drug dependence, alcohol dependence, or current medical history. (14) During the two weeks prior to the visit to the test site, the patient or his / her family members had mild wind symptoms such as fever, cough, and sore throat, high fever, dyspnea, and strong fatigue. Those who have or are currently having dysgeusia or olfactory dysfunction. (15) Subjects who plan to travel or travel for more than 2 weeks during the test period. (16) Subjects with low physical fitness who cannot exercise moderately, or subjects who have orthopedic area disease or orthopedic area chronic disease. (17) Subjects deemed inappropriate to participate in this study by the principal investigator.

Study & Design

• Study Type: Interventional
• Study Design: Not specified