Profiling the RCRSP Patient: a Pain Phenotype Classification Algorithm

Status Not yet recruiting

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

Rotator Cuff Impingement
Rotator Cuff Injuries
Rotator Cuff Syndrome
Rotator Cuff Tear or Rupture, Not Specified as Traumatic
Rotator Cuff Tears
Rotator Cuff Tendinosis
Rupture
Shoulder Impingement Syndrome
Tendinopathy

Clinical Trial Details

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

View Details

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