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A randomized placebo controlled clinical trial of a rehabilitation programme for patients with a diagnosis of massive, irreparable rotator cuff tears of the shoulder

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ISRCTN
Registry ID
ISRCTN64734872
Enrollment
60
Registered
2006-09-29
Start date
2005-09-05
Completion date
Unknown
Last updated
2015-01-13

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Musculoskeletal Diseases: Shoulder disorders Musculoskeletal Diseases Shoulder disorders

Interventions

Patients will be randomized to receive ultrasound or to receive ultrasound and a rehabilitation program. Patients randomized into the rehabilitation arm of the study will be following the rehabilitati

Sponsors

Record Provided by the NHSTCT Register - 2006 Update - Department of Health
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 60 patients with a diagnosis of irreparable rotator cuff tears will be recruited from patients referred into the South Devon Physiotherapy Service by GPs, consultants or by self referral, 30 for the exercise group and 30 for the control group. Inclusion criteria: 1. 18 years or over (no upper age limit) 2. Male or female 3. Clinical and ultrasonographic diagnosis of massive rotator cuff tear (full thickness tear of more than 5cm) 4. Diagnosis of massive, irreparable rotator cuff tear following shoulder surgery to try to repair the rotator cuff 5. Patient able to understand and co-operate with research and able to give informed consent 6. Fluent in written and spoken English

Exclusion criteria

Exclusion criteria: 1. Diagnosed neurological abnormality affecting the shoulder joint complex 2. Patients involved in an industrial claim or litigation 3. Patients whose rotator cuff tear is considered to be operable

Design outcomes

Primary

MeasureTime frame
To use the information collected to improve the rehabilitation programme and to increase awareness of which patient will do well with the programme. Primary outcome measure: Oxford Shoulder Score.

Secondary

MeasureTime frame
Not provided at time of registration

Countries

United Kingdom

Outcome results

None listed

Source: ISRCTN (via WHO ICTRP) · Data processed: Feb 4, 2026