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Clinical Trial Summary

The aim of this study is to collect a sum of different characteristics that have been mentioned previously in people presenting with RCRSP and by clustering them to create a phenotype system which may assist the individualisation of their management


Clinical Trial Description

This study will be conducted at a hospital environment by recruiting people that will seek help for their shoulder pain by a specialist upper- limb Orthopaedic Surgeon at the Department of Hand & Upper Limb Microsurgery of the 'KAT General Hospital' in Athens, Greece. Participants that will be diagnosed with RCRSP by the orthopaedic surgeon and fulfil the eligibility criteria will undergo a series of one-off measurements. Written consent will have to be obtained before a sum of self-reported outcome measures and objective testing will take place. The main categories for which outcome measures will be used are: pain, function, psychosocial and lifestyle factors. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05817578
Study type Observational
Source Clinical Exercise Physiology and Rehabilitation Reasearch Laboratory
Contact ACHILLEAS PALIOURAS, PT, MSc
Phone 6975768673
Email apaliouras@uth.gr
Status Not yet recruiting
Phase
Start date September 2, 2023
Completion date September 30, 2024

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