Clinical Trial: Development of a method for evaluating the transverse arch of the midfoot and examination of its relationship with foot and ankle kinematics during movement (Japan)

Tokyo, Sept. 1 -- UMIN Clinical Trials Registry (UMIN-CTR) received information related to the study (UMIN000058751) titled 'Development of a method for evaluating the transverse arch of the midfoot and examination of its relationship with foot and ankle kinematics during movement' on Sept. 1.

Study Type: Interventional

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

Primary Sponsor: Institute - Niigata University of Health and Welfare

Condition: Condition - healthy person Classification by malignancy - Others Genomic information - NO

Objective: Narrative objectives1 - 1. Calculate indicators related to the transverse arch of the midfoot using magnetic resonance imaging (MRI) and verify their validity against measurements taken with a three-dimensional foot moulding device. 2. Confirm the relationship between the flexibility of the transverse arch of the midfoot and joint movement and balance ability during movement. Basic objectives2 - Efficacy

Intervention: Interventions/Control_1 - MRI imaging (number of sessions: 1, time restraint: 2.5 hours, imaging site: foot and ankle joint) Foot morphometric evaluation Three-dimensional movement analysis (gait and sports-related movements) Interventions/Control_2 - MRI imaging (number of sessions: 1, time restraint: 2.5 hours, imaging site: foot and ankle joint) Foot morphometric evaluation Three-dimensional movement analysis (gait and sports-related movements)

Eligibility: Age-lower limit - 18 years-old = Gender - Male and Female Key inclusion criteria - 1. men and women aged 18 years and over and under 30 years at the time of obtaining consent 2. who do not have any orthopaedic disease of the lower limbs at the time of obtaining consent 3. who can give written consent to participate in this study Key exclusion criteria - 1. persons with orthopedic conditions of the lower limbs at the time of obtaining consent 2. who wear metal objects that cannot be removed 3. who are claustrophobic or resistant to enclosed spaces Target Size - 180

Recruitment Status: Recruitment status - Preinitiation Date of protocol fixation - 2025 Year 08 Month 09 Day Anticipated trial start date - 2025 Year 09 Month 01 Day Last follow-up date - 2028 Year 03 Month 31 Day

To know more, visit https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000067177

Disclaimer: Curated by HT Syndication.