Profiling Patients With Rotator Cuff Related Shoulder Pain: What Factors Influence Outcomes With Non-operative Care in a Secondary Care Specialist Shoulder Clinic?

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18+
SponsorUniversity of Limerick

About this trial

Shoulder pain from rotator cuff disorders is common, affecting function and quality of life. Many patients in orthopaedic clinics are diagnosed with these conditions. Most do not need surgery and are treated with pain relief and physiotherapy. However, long physiotherapy waitlists cause delays, and some patients do not achieve good outcomes. There is limited evidence to predict who will recover well with non-surgical care.

A cohort study at Croom Orthopaedic Hospital is proposed to explore this. Patients assessed as suitable for non-surgical care by the shoulder physiotherapist will provide consent and complete questionnaires on pain, disability, quality of life, and personal factors like age and gender. They will continue with prescribed care and repeat the questionnaires after six months.

This study will identify factors predicting successful outcomes, improving treatment programs to better meet patients' needs. It is funded by the Irish Research Council and led by Professors Karen McCreesh and Rose Galvin, UL, and Mr. Tristan Cassidy, Orthopaedic Consultant. Collaborators include Catriona Foley, shoulder specialist physiotherapist at Croom.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Adults

Clinically diagnosed Rotator Cuff Related Shoulder Pain (disorder of the rotator cuff muscles and/or sub acromial space).

Being referred to primary care physiotherapy or other non-surgical management.

Disqualifiers

Under 18

Non-rotator cuff related pathologies of the shoulder such as fractures, frozen shoulder, concomitant neck pain.

Person undergoing shoulder surgery.

Neither the patient nor carer can communicate in English sufficiently to complete consent or baseline assessment.

Trial population

All adults who present to the Specialist Shoulder clinic at Croom Orthopaedic Hospital between January 2026 and January 2027 (inclusive) will be considered eligible for inclusion to the study provided that they meet the inclusion criteria outlined above.

Trial design

Design model

Cohort

Time perspective

Prospective

Treatments tested in this trial

Not listed

Trial groups

150 Participants
are grouped into 1 trial group
Group A: Non-operatively managed Rotator Cuff Related Shoulder Pain patients

Trial outcomes

Primary outcomes

1

Pain Visual Analogue Scale (VAS)

Pain level on a scale from 0-10. 0 = no pain, 10 = worst pain. higher number = worse

Time frame
From enrollment to six month follow up
2

Shoulder Pain and Disability Index (SPADI)

Shoulder Pain and Disability Index measures a patient's self-perceived pain and functional limitations due to shoulder problems. 0 = no pain/disability 100 = maximum pain/disability Higher scores = worse outcome

Time frame
From enrollment to six month follow up
3

Western Ontario Rotator Cuff Index (WORC)

Western Ontario Rotator Cuff Index measures the impact of rotator cuff conditions on a person's quality of life. Scored from 0-2100. 0 = best (no impairment) 2100 = worst (maximum impairment)

Time frame
From enrollment to six month follow up

Secondary outcomes

Other outcomes

Sponsors and contacts

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