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Investigation of the Effectiveness of Flossing in Hemiplegic Patients With Shoulder Pain

This study aims to contribute to clinical practice by investigating the effectiveness of flossband application on range of motion, functionality, pain and sleep quality in hemiplegic patients with shoulder pain.

Condition(s)Shoulder Pain, Hemiplegia
StatusRecruiting
PhaseNA
Study typeInterventional
SummaryThis study aims to contribute to clinical practice by investigating the effectiveness of flossband application on range of motion, functionality, pain and sleep quality in hemiplegic patients with shoulder pain.
Who can participateInclusion Criteria * Individuals with a clinical diagnosis of stroke * Individuals between the ages of 30 and 55 * Individuals experiencing hemiplegic shoulder pain (VAS ≥ 3) and/or limited joint movement * Individuals who have been at least 6 months post-stroke (chronic phase) * Individuals who have an active range of motion of at least 90° in shoulder flexion and abduction * Individuals with stable vital signs * Individuals who volunteer to participate in the study and who understand the purpose and process of the study and sign a written informed consent form Exclusion Criteria * Presence of serious orthopedic problems such as shoulder fractures, dislocations, or rotator cuff tears * Presence of skin lesions or circulatory disorders that may prevent flossband application * Spasticity in
Ages30 Years to 55 Years
SexAll
Accepts healthy volunteersYes
Lead sponsorUskudar University
LocationsIstanbul, Turkey (Türkiye)
Start date2025-12-03
NCT IDNCT07261007
Official listinghttps://clinicaltrials.gov/study/NCT07261007

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