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Exercise Training Sequence for Subacromial Impingement Syndrome

The University of Texas System (UT) logo

The University of Texas System (UT)

Status

Completed

Conditions

Subacromial Impingement Syndrome

Treatments

Other: Scapular Training
Other: Rotator Cuff Training

Study type

Interventional

Funder types

Other

Identifiers

NCT02478567
052012-017

Details and patient eligibility

About

Randomized crossover trial evaluating the impact of exercise training sequence of axioscapular and rotator cuff exercises in patients diagnosed with subacromial impingement syndrome.

Full description

While physical therapy is an effective element in the rehabilitation of rotator cuff (RC) disease, the most effective sequence of training interventions has not been defined. The purpose of this study is to determine if there is a difference in pain or function in patients who are given RC strengthening prior to or after initiating scapular stabilization exercises.

The study was a prospective randomized crossover design. 26 men and 14 women, mean age 51, diagnosed with subacromial impingement syndrome (SAIS) were randomly assigned to one of two groups for a comprehensive and standardized rehabilitation program over six visits at an orthopedic outpatient clinic. One group was prescribed a 4-week program of scapular stabilization exercises while the other group began with RC strengthening exercises. The crossover design had each group add the previously excluded four exercises to their second month of rehabilitation.

Enrollment

40 patients

Sex

All

Ages

18 to 80 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • 18-80 years of age
  • diagnosis of Neer Stage I/II subacromial impingement with a primary pain complaint in the shoulder and/or upper arm
  • presence of at least two of the following findings: painful arc, weakness in external rotation, positive impingement sign (Hawkins-Kennedy or Neer/Walsh tests), pain and/or weakness with resistance to internal rotation, external rotation, or scapular plane elevation.

Exclusion criteria

  • concurrent medical co-morbidities including pregnancy, diabetes, and rheumatoid arthritis -
  • osteoarthritis greater than grade 2 on the Kellgren-Lawrence scale
  • current diagnosis and/or previous history of glenohumeral instability or dislocation
  • full-thickness rotator cuff tear
  • adhesive capsulitis
  • fractures of the scapula, clavicle or humerus
  • scapulothoracic or rotator cuff paresis
  • shoulder surgery in past year
  • inability to speak the English language at a level sufficient to obtain informed consent.

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Crossover Assignment

Masking

Single Blind

40 participants in 2 patient groups

Scapular Training
Experimental group
Description:
Initiated scapular training exercise for the first 4 weeks followed by addition of rotator cuff exercises the next four weeks
Treatment:
Other: Scapular Training
Rotator Cuff Training
Experimental group
Description:
initiated rotator cuff training exercise for the first 4 weeks followed by addition of scapular training exercises the next four weeks.
Treatment:
Other: Rotator Cuff Training

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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