Tokyo, Oct. 15 -- UMIN Clinical Trials Registry (UMIN-CTR) received information related to the study (UMIN000059389) titled 'The effect of a health program incorporating supplemental intake for body composition enhancement on weight loss outcomes' on Oct. 14.

Study Type: Interventional

Study Design: Basic Design - Single arm Randomization - Non-randomized Blinding - Open -no one is blinded Control - Uncontrolled

Primary Sponsor: Institute - Healthcare Systems Co., Ltd.

Condition: Condition - Healthy Adults Classification by malignancy - Others Genomic information - NO

Objective: Narrative objectives1 - To exploratively evaluate the slimming effects of a health program incorporating supplemental intake for body composition enhancement, conducted for four weeks in adult men and women aged 20 to 59 with a slightly high BMI. Basic objectives2 - Efficacy

Intervention: Interventions/Control_1 - In this study, participants will participate in the following health program daily for four weeks.

Meal 1: Take one packet of the test food (XS Burn Fit Powder) daily before exercise. Meal 2: Limit daily calorie intake to 1,800 kcal for men and 1,400 kcal for women. Exercise: Approximately 10 minutes of designated exercise (XS Fitness) and at least 8,000 steps of walking.

Eligibility: Age-lower limit - 20 years-old = Gender - Male and Female Key inclusion criteria - 1.Persons who have been fully informed of the purpose and content of this research, have the capacity to consent, fully understand, and freely and voluntarily volunteer to participate in this research, and agree to participate in the study 2.Persons who are Japanese adults, male and female, aged 20 or older and under 60 at the time of consent, and whose BMI is classified as slightly high Key exclusion criteria - 1.Persons who have chronic illness, receiving medication, have a serious disease history 2.Persons who have a BMI of 30 or higher 3.Persons who have exercised regularly within the last year (e.g., jogging, gym training, sports, etc.) 4.Persons who are allergic to the test food 5.Persons who have a fructose metabolism disorder 6.Persons who usually take a large amount of test food 7.Persons who usually take medicine, specified health food, healthy food and supplements that may have effect to lipid metabolism 8.Persons who have participated in other tests within the first month before the start of the test, or those who intend to participate in another exam after consenting to this exam 9.Persons who are judged to be ineligible by the supervising doctor or the principal investigator 10.Persons who are pregnant, planning or hoping to be pregnant during the study period, breastfeeding Target Size - 20

Recruitment Status: Recruitment status - Preinitiation Date of protocol fixation - 2025 Year 10 Month 07 Day Anticipated trial start date - 2025 Year 11 Month 04 Day Last follow-up date - 2026 Year 01 Month 31 Day

To know more, visit https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000067930

Disclaimer: Curated by HT Syndication.