What factors influence recovery with non-surgical care for rotator cuff shoulder pain?
Official title: Profiling Patients With Rotator Cuff Related Shoulder Pain: What Factors Influence Outcomes With Non-operative Care in a Secondary Care Specialist Shoulder Clinic?
Run by University of Limerick · NCT07360847 · Data updated 2026-11-12
This project will try to find which patient characteristics predict who improves with non-surgical care for rotator cuff related shoulder pain.
Quick facts
| Study type | Observational |
|---|---|
| Ages | 18 Years and up |
| Sex | All |
| Enrollment | 150 (estimated) |
| Sponsor | University of Limerick Academic / other |
| Locations | 1 site (Limerick) |
| Status | Recruiting |
| Started | January 5, 2026 |
| Main results expected | January 1, 2027 |
| Study ends | November 1, 2027 |
| Registry record updated | March 27, 2026 |
| Trial ID | NCT07360847 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Adults with a clinical diagnosis of rotator cuff related shoulder pain who are referred for non-operative management at the Croom Orthopaedic Hospital and can consent and complete English-language questionnaires.
✕Probably not a fit
People under 18, those with non-rotator cuff shoulder pathologies, patients already undergoing shoulder surgery, or those unable to complete consent/questionnaires in English are not eligible and unlikely to benefit from this work.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
This prospective cohort will enroll adults attending a secondary-care shoulder clinic in Croom, Limerick, who are judged suitable for non-operative management. Participants will complete baseline questionnaires on pain, disability, quality of life, and personal factors such as age, sex, comorbidities and symptom duration, then follow their prescribed non-surgical care. Outcomes will be re-measured at six months and analyzed to identify which baseline factors are associated with better or worse recovery. The results are intended to inform targeted treatment pathways and reduce delays or unnecessary surgical referrals.
Why it matters
Potential benefit: If successful, the study could help match patients to the non-surgical treatments most likely to work for them, shorten ineffective care pathways, and reduce unnecessary surgeries.
How similar studies have gone: Non-surgical management for rotator cuff disorders is supported by prior trials, and some cohort studies have reported predictors such as higher baseline pain, longer symptom duration, and comorbidities, but robust prognostic data from secondary-care clinics remain limited.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: * 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. Exclusion Criteria: * 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.
Where it's running
-
Croom Orthopaedic Hospital
Limerick, Ireland Recruiting
Study contacts
- Study coordinator: Roisin Cahill, MSc Physiotherapy
- Email: cahill.roisin@ul.ie
- Phone: +353 858216254
Similar studies
Other studies for the same condition or treatment. Recruiting studies are listed first.
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Night Pain Module for Rotator Cuff-Related Shoulder Pain
Researchers are testing a short set of questions to measure night pain in people with rotator cuff–related shoulder pain to see if it reliably describes how sleep is affected.
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Nociplastic Pain in SAPS: A Look at Pain Types in Shoulder Pain
This study tests how common nociplastic pain is among people with subacromial pain syndrome who have shoulder pain for at least 3 months.
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Pain phenotype and response to corticosteroid injection in SAPS
This study tests whether people with subacromial pain syndrome who have a nociplastic pain pattern respond differently to a corticosteroid injection than those without that pattern.
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Attention-shift exercise program for rotator cuff–related shoulder pain
This will test whether doing shoulder exercises while also performing attention-shifting movements reduces pain and improves function for people with rotator cuff-related shoulder pain.
-
Contextually Enhanced Exercise Program for Rotator Cuff‑Related Shoulder Pain
This trial tests whether adding personalized contextual factors to a proven exercise program helps people with rotator cuff–related shoulder pain feel less pain and move better.
-
Dual-task shoulder exercise program for rotator cuff–related pain
This trial tests whether doing shoulder exercises together with simple cognitive tasks helps adults with rotator cuff–related shoulder pain reduce pain and improve function compared with standard shoulder exercises.
How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.