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Effects of Supervised Physical Therapy With Early Activation of the Rotator Cuff Versus Home Exercises in Patients After Arthroscopic Subacromial Decompression

Effects of Supervised Physical Therapy With Early Activation of the Rotator Cuff Versus Home Exercises in Patients After Arthroscopic Subacromial Decompression

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01054326
Enrollment
45
Registered
2010-01-22
Start date
2003-01-31
Completion date
2007-01-31
Last updated
2010-01-22

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

Conditions

Subacromial Decompression

Keywords

arthroscopic subacromial decompression, exercise, physical therapy, rotator cuff, shoulder impingement syndrome, Subacromial impingement after arthroscopic subacromial decompression

Brief summary

The objective of this study was to evaluate and compare two different post-surgical rehabilitation strategies, Rehabilitation supervised by a physical therapist including exercises with progressive early activation of the rotator cuff versus basic home exercises regarding shoulder function, pain, health related quality of life and return to work after arthroscopic subacromial decompression.

Detailed description

Patients scheduled for surgery (arthroscopic subacromial decompression)and in the age 25-65 were offered to participate in the study. After surgery they were randomized to either Supervised Physical therapy with early activation of the rotator cuff (PT-group) or to home exercises (H-group). Patients in the PT group met the physical therapist twice a week for exercises and in between these visits they did their exercises at home daily. The H-group did home exercises daily. Shoulder function and pain(primary outcomes)and health related quality of life, returning to work(secondary outcomes)were assessed before surgery, one week after(baseline), 1,2,3 and 6 months after surgery by an independent physical therapist.

Interventions

OTHERExercises

Sponsors

Kalmar County Hospital
CollaboratorOTHER
Linkoeping University
Lead SponsorOTHER_GOV

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Investigator)

Eligibility

Sex/Gender
ALL
Age
25 Years to 65 Years
Healthy volunteers
No

Inclusion criteria

* Subacromial impingement verified with Neer impingement test * At least 6 month duration of pain * Treated in primary care without satisfactory results for at least three months. * Typical history and pain location. Scheduled for surgery (subacromial decompression) * Three of these four tests must be positive: * Neer impingement test * Hawkins-Kennedy impingement sign Jobe supraspinatus test * Painful arc 60-120 degree

Exclusion criteria

* Radiological findings of malignancy osteoarthritis, fractures * Polyarthritis or fibromyalgia * Pathological hyper laxity * Lack of communication skills that prevent the use of outcome measurements * Cervical spine pathology

Design outcomes

Primary

MeasureTime frame
Shoulder function and painbefore surgery, 1 w (baseline, 1,2,3 and 6 month after surgery

Secondary

MeasureTime frame
Health related quality of life and returning to workbefore surhery and 1 w(baseline)1,2,3 and 6 months after surgery

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026