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Completed

NCT Number: NCT01054326

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

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.

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Key information

Age range

25 year–65 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

About this study

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.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

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

Treatment and study plan

Exercises

Other

Primary outcomes

  1. Shoulder function and pain

    Time frame: before surgery, 1 w (baseline, 1,2,3 and 6 month after surgery

Secondary outcomes

  1. Health related quality of life and returning to work

    Time frame: before surhery and 1 w(baseline)1,2,3 and 6 months after surgery

Sponsors and collaborators

Lead sponsor

Linkoeping University

Other Gov

Collaborators

  • Kalmar County Hospital

Registry information

Important dates

Study start
2003
Primary completion
2006
Study completion
2007
First posted
Jan 22, 2010
Registry last updated
Jan 22, 2010

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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