Cross-sectorial Use of Patient-Reported Outcomes in Chronic Degenerative Shoulder Conditions
Key facts
- Where
- Charlottenlund, Gentofte Municipality, Hellerup, and Rødovre Municipality, DenmarkSee the 6 sites
Could this be for you?
Answer for yourself. This is not a decision: only the study team can say whether you can take part.
- Are you between 18 and 120 years old?
Source: NCT06435494, who can take part
Where in Denmark
- Privathospitalet DanmarkCharlottenlund, DenmarkNo longer taking part
- Department of Physiotherapy, Univesity Hospital GentofteGentofte Municipality, DenmarkNo longer taking part
- Department of rehabilitation, Gentofte KommuneHellerup, DenmarkNo longer taking part
- Division of shoulder and elbow surgery, Department of orthopaedics, Univesity Hospital GentofteHellerup, DenmarkNo longer taking part
- Genoptræning og Rehabilitering, Rødovre KommuneRødovre Municipality, DenmarkNo longer taking part
- Mit LægehusRødovre Municipality, DenmarkNo longer taking part
Questions to ask the study team
- How often do I need to come in, and for how long each time?
- Are travel costs paid?
- Can I keep my own doctor?
- What happens if I want to stop?
Contact the study team: see the registry record → Contacts and Locations
Print a page for my doctorTrial details
- Who runs it
- University Hospital, Gentofte, Copenhagen
- Trial code
- NCT06435494
- Record updated
- 2 April 2025
- Original description
This research project aims to test if systematic (extensive) use of patient-reported outcomes across treatment boundaries canRead full original descriptionShow less
C-PRO - The Effect of Cross-sectorial Use of Patient-Reported Outcomes for Patients With Chronic Degenerative Shoulder Conditions
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.
Inclusion: shoulder pain with no acute trauma.
Exclusion: Psychiatric conditions, mental conditions and substance abuse that might affect the ability to provide informed consent or responding to PROMs; Disseminated malignant condition, other serious medical conditions or other life crisis where the focus on a shoulder research project is unreasonable; Age <18 years; Non-Danish citizenship; Unable to understand written or spoken Danish; Inability to master electronic means of communication and/or not having an electronic communication (E-boks); Employee at participating centre or other relation to participating health professionals that might affect independent consent; Already included in the study with the contralateral shoulder.