Tokyo, May 30 -- UMIN Clinical Trials Registry (UMIN-CTR) received information related to the study (UMIN000059123) titled 'A study to investigate the effects of resistance training combined with supplementation of functional food ingredient on abdominal skeletal muscle mass and quality in women' on May 30.

Study Type: Interventional

Study Design: Basic Design - Parallel Randomization - Randomized Blinding - Double blind -all involved are blinded Control - Placebo

Primary Sponsor: Institute - Juntendo University

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

Objective: Narrative objectives1 - Evaluation of the effects of resistance training combined with supplementation of functional food ingredient on abdominal skeletal muscle mass and quality in women Basic objectives2 - Efficacy

Intervention: Interventions/Control_1 - Intake of test food containing lemon myrtle extract for 8 weeks combined with resistance training for 8 weeks. Interventions/Control_2 - Intake of test food not containing lemon myrtle extract for 8 weeks combined with resistance training for 8 weeks.

Eligibility: Age-lower limit - 30 years-old = Gender - Female Key inclusion criteria - 1.Subjects who are healthy women aged 30 to 59 2.Subjects with a BMI ranging from 18.5 to less than 30.0 3.Subjects who are aware of worse of abdominal muscles or getting increase of abdominal fat Key exclusion criteria - 1.Subjects who regularly engage in resistance training or endurance exercises 2.Subjects who regularly attend fitness facilities, including yoga or pilates classes 3.Subjects who have symptoms that interfere with training, such as lower back pain or arthralgia 4.Subjects who are currently on a diet involving dietary restrictions or similar weight-loss efforts 5.Subjects who have undergone, or plan to undergo, cosmetic medicine for weight loss, such as liposuction, medication, or injections 6.Subjects who take functional foods or supplements in order to improve of symptoms related to muscle or arthrosis on a daily basis 7.Subjects who have participated in clinical trials with exercises within the past year, or clinical trials with intake of pharmaceuticals or food ingredients within the past three month 8.Subjects who are considerably undernutrition 9.Subjects who are currently pregnant 10.Subjects who are judged to be ineligible by a doctor. Target Size - 30

Recruitment Status: Recruitment status - Preinitiation Date of protocol fixation - 2025 Year 08 Month 01 Day Date of IRB - 2025 Year 08 Month 01 Day Anticipated trial start date - 2025 Year 10 Month 01 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=R000067633

Disclaimer: Curated by HT Syndication.