Clinical trial Recruiting at 1 site Observational Ages 18 and up

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.

More Rotator Cuff Related Shoulder Pain trials

Quick facts

Study typeObservational
Ages18 Years and up
SexAll
Enrollment150 (estimated)
SponsorUniversity of Limerick
Academic / other
Locations1 site (Limerick)
StatusRecruiting
StartedJanuary 5, 2026
Main results expectedJanuary 1, 2027
Study endsNovember 1, 2027
Registry record updatedMarch 27, 2026
Trial IDNCT07360847 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

Similar studies

Other studies for the same condition or treatment. Recruiting studies are listed first.

How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.