Tokyo, Dec. 1 -- UMIN Clinical Trials Registry (UMIN-CTR) received information related to the study (UMIN000059187) titled 'A Study on the Effectiveness of Self-Evaluation and Corrective Exercises for Physical Function' on Dec. 1.
Study Type:
Interventional
Study Design:
Basic Design - Single arm
Randomization - Non-randomized
Blinding - Open -no one is blinded
Control - Self control
Primary Sponsor:
Institute - Sapporo Medical University
Condition:
Condition - musculoskeletal disorders, individuals with nonspecific complaints, lifestyle-related diseases
Classification by malignancy - Others
Genomic information - NO
Objective:
Narrative objectives1 - To assess the impact of Self-Evaluation and Corrective Exercises for integration into education and public health.
Basic objectives2 - Efficacy
Intervention:
Interventions/Control_1 - corrective exercise
Eligibility:
Age-lower limit - 18
years-old
Gender - Male and Female
Key inclusion criteria - Individuals capable of performing light exercise who have provided informed consent to participate in the study
Key exclusion criteria - Exclusion Criteria:
- Individuals instructed by a physician to restrict physical activity
- Those with uncontrolled severe cardiovascular, respiratory, or neurological disorders
- Individuals with paroxysmal conditions (including syncope) who have not received medical clearance for exercise
- Those with neuromuscular disorders or severe balance impairments posing a high risk of falls
- Individuals for whom exercise is not recommended due to eating disorders, energy deficiency, or related conditions
- Pregnant individuals or those within three months postpartum
- Individuals with impaired capacity to provide informed consent or insufficient comprehension of Japanese
- Individuals under the age of 18
Temporary Exclusion:
Participants experiencing acute injury or postoperative status, active inflammation or fever, moderate to severe pain, uncontrolled metabolic abnormalities, marked palpitations or shortness of breath, extreme fatigue, dizziness, or intoxication will be temporarily excluded. They may be enrolled upon recovery or with approval from their attending physician.
Operational Exclusion:
Participants will be excluded if follow-up Self-Check assessments are not feasible or if consent is withdrawn.
Target Size - 220
Recruitment Status:
Recruitment status - Preinitiation
Date of protocol fixation - 2025 Year 12 Month 01 Day
Anticipated trial start date - 2025 Year 12 Month 09 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=R000067694
Disclaimer: Curated by HT Syndication.