Tokyo, July 10 -- UMIN Clinical Trials Registry (UMIN-CTR) received information related to the study (UMIN000058403) titled 'Carotid artery wall thickness and physical measurements and nutritional intake in young women' on July 10.

Study Type: Interventional

Study Design: Basic Design - Parallel Randomization - Non-randomized Blinding - Open -no one is blinded Control - No treatment

Primary Sponsor: Institute - Kagawa Nutrition University

Condition: Condition - lifestyle disease Classification by malignancy - Others Genomic information - NO

Objective: Narrative objectives1 - The subjects were young and middle-aged women.They will be asked to directly measure the vascular status of the carotid artery wall and to write physical measurements, blood tests, urinalysis, and a 3-day dietary record.We will compare the age at which atherosclerosis, an indicator of lifestyle-related diseases, begins to occur. Basic objectives2 - Others

Intervention: Interventions/Control_1 - For young women, carotid echocardiography will be performed on college students 18-30 years of age.Physical measurements, blood tests, and a written 3-day dietary record will be taken. Interventions/Control_2 - For middle-aged and older women, carotid artery echocardiography will be performed in subjects between 40 and 85 years of age.Physical measurements, blood tests, and a written 3-day dietary record will be taken.

Eligibility: Age-lower limit - 18 years-old = Gender - Female Key inclusion criteria - 1.Healthy individuals with no serious diseases. 2.Women between the ages of 18 and 75 who voluntarily wish to participate in the clinical trial and provide written consent. 3.Those who are able to maintain a certain daily lifestyle during the study period. 4.Those who are being treated for mild chronic diseases (hypertension, hyperlipidemia, etc.) may participate in the study at the discretion of the study investigator. Key exclusion criteria - 1)Patients with serious diseases (cardiac, hepatic, renal, cancer, etc.) or mental disorders 2)Those with a history of digestive system diseases or digestive organ surgeries 3)Those who are unable to maintain their daily lifestyle with significant changes in diet and physical activity 4)Pregnant or lactating women and those who wish to become pregnant during the study period 5)Other patients who are deemed ineligible by the investigator to participate in this study. 6)Those who have participated in other clinical trials within the past month. Target Size - 200

Recruitment Status: Recruitment status - Open public recruiting Date of protocol fixation - 2025 Year 06 Month 16 Day Date of IRB - 2025 Year 06 Month 16 Day Anticipated trial start date - 2025 Year 06 Month 20 Day Last follow-up date - 2030 Year 03 Month 31 Day

To know more, visit https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000066768

Disclaimer: Curated by HT Syndication.