Clinical Trial: Characteristics of Shoulder Range of Motion and Functional Impairment in Patients with Shoulder Joint Disorders Who Underwent Rehabilitation at Our Hospital: A Retrospective Study (Japan)

Tokyo, July 1 -- UMIN Clinical Trials Registry (UMIN-CTR) received information related to the study (UMIN000061769) titled 'Characteristics of Shoulder Range of Motion and Functional Impairment in Patients with Shoulder Joint Disorders Who Underwent Rehabilitation at Our Hospital: A Retrospective Study' on July 1.

Study Type: Observational

Primary Sponsor: Institute - Saitama Medical University Kawagoe Clinic

Condition: Condition - shoulder impingement syndrome, shoulder contracture, periarthritis of the shoulder, calcific tendinitis of the shoulder, rotator cuff injury of the shoulder, rotator cuff tear of the shoulder, unstable shoulder joint, osteoarthritis of the shoulder, adhesive capsulitis of the shoulder, traumatic arthritis of the shoulder, and rheumatoid Classification by malignancy - Others Genomic information - NO

Objective: Narrative objectives1 - The purpose of this study is to conduct a retrospective analysis of changes over time in shoulder range of motion, pain, and functional impairment among patients with shoulder joint disorders who underwent rehabilitation at our hospital, and to clarify the relationship between clinical improvement on the SPADI and the duration of rehabilitation intervention as well as patient background factors. Basic objectives2 - Efficacy

Eligibility: Age-lower limit - 18 years-old <= Age-upper limit - Not applicable Gender - Male and Female Key inclusion criteria - Cases diagnosed with shoulder impingement syndrome, adhesive capsulitis, frozen shoulder, calcific tendinitis of the shoulder, rotator cuff injury, rotator cuff tear, shoulder instability, osteoarthritis of the shoulder, adhesive shoulder capsulitis, traumatic shoulder arthritis, and rheumatoid arthritis at our clinic. Key exclusion criteria - Individuals with fractures around the shoulder joint or shoulder dislocation.Individuals who underwent surgery based on the aforementioned diagnoses.Individuals who received rehabilitation at other facilities for the aforementioned diagnoses.Individuals who expressed refusal to participate in this study through information disclosure documents.Individuals deemed unsuitable by the principal investigator. Target Size - 300

Recruitment Status: Recruitment status - Preinitiation Date of protocol fixation - 2026 Year 07 Month 01 Day Anticipated trial start date - 2026 Year 07 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=R000070655

Disclaimer: Curated by HT Syndication.