Tokyo, June 10 -- UMIN Clinical Trials Registry (UMIN-CTR) received information related to the study (UMIN000061845) titled 'Study on the Effects of Floating Toe on Posture, Gait, and Jump Performance' on June 10.

Study Type: Interventional

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

Primary Sponsor: Institute - Niigata University of Health and Welfare

Condition: Condition - Floating Toe Classification by malignancy - Others Genomic information - NO

Objective: Narrative objectives1 - To investigate the effects of floating toe on static and dynamic postural stability, gait initiation, stepping performance, and jumping performance in healthy young adults. Basic objectives2 - Efficacy

Intervention: Interventions/Control_1 - Participants without floating toe will be assessed under a normal condition and a simulated floating toe condition using research insoles or research shoes. Static and dynamic postural stability, plantar pressure distribution, gait initiation, stepping performance, and jumping performance will be measured. The intervention will be performed only on the day of assessment, and the use of the research insoles or shoes will be limited to the measurement tasks. Each detailed experiment will take approximately 60-90 minutes and will be conducted up to two times per participant.

Eligibility: Age-lower limit - 18 years-old = Gender - Male and Female Key inclusion criteria - 1.Healthy men and women aged 18 to 30 years. 2.Individuals who understand the explanation of the study and provide written informed consent. 3.University students, technical college students, athletes, or adults participating in community sports clubs or similar organizations. Key exclusion criteria - 1.Individuals with acute lower limb injury or worsening lower limb pain. 2.Individuals who have recently undergone lower limb surgery. 3.Individuals with neurological disorders or severe cardiovascular disease. 4.Individuals who are pregnant or judged to require special safety consideration. 5.Individuals who are in poor physical condition on the day of measurement. 6.Individuals judged by the principal investigator to be inappropriate for participation in the study. Target Size - 300

Recruitment Status: Recruitment status - Preinitiation Date of protocol fixation - 2026 Year 06 Month 15 Day Anticipated trial start date - 2026 Year 07 Month 01 Day Last follow-up date - 2027 Year 03 Month 31 Day

To know more, visit https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000070765

Disclaimer: Curated by HT Syndication.