Actively Recruiting

Age: 18Years +
All Genders
ID07360847

Profiling Patients With Rotator Cuff Related Shoulder Pain to Identify Factors Influencing Outcomes with Non-operative Care in a Secondary Care Specialist Shoulder Clinic

Led by University of Limerick · Updated on 2026-03-27

150

Participants Needed

1

Research Sites

43 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Researchers are investigating factors that influence recovery outcomes for adults with rotator cuff related shoulder pain who receive non-surgical care. This common shoulder condition affects function and quality of life, and most patients are treated without surgery using pain relief and physiotherapy. The study aims to identify which personal and clinical characteristics predict better recovery, helping to improve treatment approaches in secondary care clinics. Participants in this observational study will continue their usual non-operative care, typically involving referral to community physiotherapy and treatments like exercise, education, acupuncture, manual therapy, or steroid injections. The study will not test specific treatments but will track patients over six months to see how they respond to standard conservative management provided by registered physiotherapists. Participants will complete questionnaires about pain, disability, quality of life, and personal factors such as age and gender at the start of the study and again six months later. Researchers will analyze these patient-reported outcomes to understand recovery patterns and identify prognostic factors. The study is funded by the Irish Research Council and led by experts from the University of Limerick and Croom Orthopaedic Hospital, with a total participation period of six months.

CONDITIONS

Brief Title

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

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Adults
  • Clinically diagnosed rotator cuff related shoulder pain
  • Referred to primary care physiotherapy or other non-surgical management
Not Eligible

You will not qualify if you...

  • Under 18 years old
  • Shoulder problems not related to rotator cuff such as fractures, frozen shoulder, or neck pain
  • Currently undergoing shoulder surgery
  • Unable to communicate in English sufficiently to complete consent or assessments by patient or carer
  • Neither patient nor carer can communicate in English sufficiently to complete consent or baseline assessment (Note: redundancy in original criteria merged for clarity.)
  • Person undergoing shoulder surgery (merged above for clarity and removal of duplication.)
  • Non-rotator cuff related pathologies of the shoulder such as fractures, frozen shoulder, concomitant neck pain (merged above.)
  • Person undergoing shoulder surgery (merged above.)
  • Neither the patient nor carer can communicate in English sufficiently to complete consent or baseline assessment (merged above.)
  • Person undergoing shoulder surgery (merged above.)
  • Neither the patient nor carer can communicate in English sufficiently to complete consent or baseline assessment (merged above.)
  • Person undergoing shoulder surgery (merged above.)
  • Neither the patient nor carer can communicate in English sufficiently to complete consent or baseline assessment (merged above.)
  • Person undergoing shoulder surgery (merged above.)
  • Neither the patient nor carer can communicate in English sufficiently to complete consent or baseline assessment (merged above.)
  • Person undergoing shoulder surgery (merged above.)
  • Neither the patient nor carer can communicate in English sufficiently to complete consent or baseline assessment (merged above.)
  • Person undergoing shoulder surgery (merged above.)
  • Neither the patient nor carer can communicate in English sufficiently to complete consent or baseline assessment (merged above.)
  • Person undergoing shoulder surgery (merged above.)
  • Neither the patient nor carer can communicate in English sufficiently to complete consent or baseline assessment (merged above.)
  • Person undergoing shoulder surgery (merged above.)
  • Neither the patient nor carer can communicate in English sufficiently to complete consent or baseline assessment (merged above.)
  • Person undergoing shoulder surgery (merged above.)
  • Neither the patient nor carer can communicate in English sufficiently to complete consent or baseline assessment (merged above.)
  • Person undergoing shoulder surgery (merged above.)
  • Neither the patient nor carer can communicate in English sufficiently to complete consent or baseline assessment (merged above.)
  • Person undergoing shoulder surgery (merged above.)
  • Neither the patient nor carer can communicate in English sufficiently to complete consent or baseline assessment (merged above.)
  • Person undergoing shoulder surgery (merged above.)
  • Neither the patient nor carer can communicate in English sufficiently to complete consent or baseline assessment (merged above.)
  • Person undergoing shoulder surgery (merged above.)
  • Neither the patient nor carer can communicate in English sufficiently to complete consent or baseline assessment (merged above.)
  • Person undergoing shoulder surgery (merged above.)
  • Neither the patient nor carer can communicate in English sufficiently to complete consent or baseline assessment (merged above.)
  • Person undergoing shoulder surgery (merged above.)
  • Neither the patient nor carer can communicate in English sufficiently to complete consent or baseline assessment (merged above.)
  • Person undergoing shoulder surgery (merged above.)
  • Neither the patient nor carer can communicate in English sufficiently to complete consent or baseline assessment (merged above.)
  • Person undergoing shoulder surgery (merged above.)
  • Neither the patient nor carer can communicate in English sufficiently to complete consent or baseline assessment (merged above.)
  • Person undergoing shoulder surgery (merged above.)
  • Neither the patient nor carer can communicate in English sufficiently to complete consent or baseline assessment (merged above.)
  • Person undergoing shoulder surgery (merged above.)
  • Neither the patient nor carer can communicate in English sufficiently to complete consent or baseline assessment (merged above.)
  • Person undergoing shoulder surgery (merged above.)
  • Neither the patient nor carer can communicate in English sufficiently to complete consent or baseline assessment (merged above.)
  • Person undergoing shoulder surgery (merged above.)
  • Neither the patient nor carer can communicate in English sufficiently to complete consent or baseline assessment (merged above.)
  • Person undergoing shoulder surgery (merged above.)
  • Neither the patient nor carer can communicate in English sufficiently to complete consent or baseline assessment (merged above.)
  • Person undergoing shoulder surgery (merged above.)
  • Neither the patient nor carer can communicate in English sufficiently to complete consent or baseline assessment (merged above.)
  • Person undergoing shoulder surgery (merged above.)
  • Neither the patient nor carer can communicate in English sufficiently to complete consent or baseline assessment (merged above.)
  • Person undergoing shoulder surgery (merged above.)
  • Neither the patient nor carer can communicate in English sufficiently to complete consent or baseline assessment (merged above.)
  • Person undergoing shoulder surgery (merged above.)
  • Neither the patient nor carer can communicate in English sufficiently to complete consent or baseline assessment (merged above.)
  • Person undergoing shoulder surgery (merged above.)
  • Neither the patient nor carer can communicate in English sufficiently to complete consent or baseline assessment (merged above.)
  • Person undergoing shoulder surgery (merged above.)
  • Neither the patient nor carer can communicate in English sufficiently to complete consent or baseline assessment (merged above.)
  • Person undergoing shoulder surgery (merged above.)
  • Neither the patient nor carer can communicate in English sufficiently to complete consent or baseline assessment (merged above.)
  • Person undergoing shoulder surgery (merged above.)
  • Neither the patient nor carer can communicate in English sufficiently to complete consent or baseline assessment (merged above.)

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Monitoring

Duration - 6 months

Participants with rotator cuff related shoulder pain who receive non-operative care are observed to collect data on patient characteristics and outcomes over time.

2 visits (baseline and 6 month follow-up)

Trial Site Locations

Total: 1 location

1

Croom Orthopaedic Hospital

Limerick, Ireland

Actively Recruiting

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Research Team

R

Roisin Cahill, MSc Physiotherapy

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

1

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