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Cross-sectorial Use of Patient-Reported Outcomes in Chronic Degenerative Shoulder Conditions — C-PRO  

Shoulder Impingement Syndrome Clinical Trial

Official title:
C-PRO - The Effect of Cross-sectorial Use of Patient-Reported Outcomes for Patients With Chronic Degenerative Shoulder Conditions

Clinical Trial Summary

This research project aims to test if systematic (extensive) use of patient-reported outcomes across treatment boundaries can 1. improve patients' and health professionals' understanding of individual patients' conditions and health changes, 2. improve indications for treatment, 3. strengthen patient empowerment, and 4. reduce patients' utilization of health services. The study will be performed in the particular context of patients with chronic degenerative conditions of the shoulder. These patients are characterized by contact with numerous health professionals from different health sectors, such as general practitioner, physiotherapists and surgical referral centres, which challenges coherence and communication for the individual treatment decisions. The research project will be performed as a randomized controlled trial (RCT) with a 1-year inclusion period and two years of follow-up.

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT06435494
Study type Interventional
Source University Hospital, Gentofte, Copenhagen
Contact Anne Marie Nyholm, MD, PhD
Phone +4538673391
Email anne.marie.nyholm.01@regionh.dk
Status Not yet recruiting
Phase N/A
Start date June 1, 2024
Completion date September 1, 2030
View Details
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