Tokyo, Nov. 26 -- UMIN Clinical Trials Registry (UMIN-CTR) received information related to the study (UMIN000059878) titled 'A Study on the Assessment of Activities of Daily Living Using Motion Capture Systems' on Nov. 26.

Study Type: Interventional

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

Primary Sponsor: Institute - St. Marianna University School of Medicine

Condition: Condition - Cerebrovascular disease, neuromuscular disease, orthopedic disease, cardiovascular disease, respiratory disease, disuse syndrome, and healthy individuals Classification by malignancy - Others Genomic information - NO

Objective: Narrative objectives1 - Analyze ADL movements in healthy individuals and patients with various diseases using a markerless motion capture system. Furthermore, by comparing joint angles and joint moments derived from ADL movements using the markerless motion capture system, identify efficient movement patterns to develop optimized ADL movement instruction and training programs. Basic objectives2 - Others

Intervention: Interventions/Control_1 - Rehabilitation

Eligibility: Age-lower limit - 20 years-old = Gender - Male and Female Key inclusion criteria - Patients must meet the following inclusion criteria. Hospitalized patients with cerebrovascular disease, neuromuscular disorders, orthopedic conditions, cardiovascular disease, respiratory disorders, or disuse syndrome. Adult patients aged 20 to 100 years who can understand the study explanation. Patients who, after receiving sufficient explanation regarding participation in this study, can provide written consent based on their own free will.

Healthy individuals meeting the following inclusion criteria are eligible. Medical staff employed at Kawasaki Municipal Tama Hospital or St. Marianna University Yokohama City Western Hospital. Individuals who, after receiving sufficient explanation regarding participation in this study, can provide written consent based on their own free will. Key exclusion criteria - Individuals deemed unsuitable for participation in the study by the researcher or attending physician due to changes in their medical condition or other reasons Target Size - 203

Recruitment Status: Recruitment status - Preinitiation Date of protocol fixation - 2025 Year 11 Month 19 Day Date of IRB - 2025 Year 11 Month 19 Day Anticipated trial start date - 2025 Year 12 Month 01 Day Last follow-up date - 2030 Year 12 Month 31 Day

To know more, visit https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000068478

Disclaimer: Curated by HT Syndication.