Skip to main content
Clinical Trials/NCT02395770
NCT02395770
Completed
N/A

Effects of a Movement Training Oriented Rehabilitation Program on Symptoms, Functional Limitations and Acromiohumeral Distance in Individuals With Subacromial Pain Syndrome

Laval University1 site in 1 country29 target enrollmentJune 2013

Overview

Phase
N/A
Intervention
Not specified
Conditions
Shoulder Impingement Syndrome
Sponsor
Laval University
Enrollment
29
Locations
1
Primary Endpoint
Symptoms and functional limitations - Upper limb
Status
Completed
Last Updated
11 years ago

Overview

Brief Summary

Objectives: Evaluate the effects of a rehabilitation program based on movement training on symptoms, functional limitations and acromiohumeral distance (AHD) in individuals with SPS.

Methods: Twenty-five participants with SPS participated in a 6-week program. Outcomes of both groups were evaluated at baseline and 6 weeks. Changes in symptoms and functional limitations were assessed. Changes in AHD for both groups were assessed using ultrasonographic measures.

Detailed Description

Background: Multiple factors have been associated with the presence of a subacromial pain syndrome (SPS), including deficits in performance of scapular and glenohumeral muscles. Such deficits can lead to inadequate kinematics and decreased acromiohumeral distance (AHD). Exercises that aim at correcting these deficits, such as movement training, were suggested to improve symptoms and functional limitations. To date, few studies have assessed outcomes following an intervention focused on movement training. Objectives: Evaluate the effects of a rehabilitation program based on movement training on symptoms, functional limitations and AHD in individuals with SPS. Design: Prospective single group pre-post design. Methods: Twenty-five participants with SPS (SPS group) participated in a 6-week program. Twenty asymptomatic volunteers were recruited for normative AHD values (control group). Outcomes of both groups were evaluated at baseline and 6 weeks, i.e. immediately following intervention for the SPS group. Changes in symptoms and functional limitations for SPS group were assessed using the Western Ontario Rotator Cuff index (WORC) and Disability of the Arm Shoulder and Hand questionnaire (DASH). Changes in AHD for both groups were assessed using ultrasonographic measures.

Registry
clinicaltrials.gov
Start Date
June 2013
End Date
September 2014
Last Updated
11 years ago
Study Type
Interventional
Study Design
Single Group
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • painful arc of movement during flexion or abduction
  • positive Neer or Kennedy-Hawkins impingement signs
  • pain on resisted lateral rotation, abduction or empty can test.

Exclusion Criteria

  • previous shoulder surgery
  • shoulder pain reproduced by neck movement
  • clinical signs of full-thickness RC tears
  • shoulder capsulitis.

Outcomes

Primary Outcomes

Symptoms and functional limitations - Upper limb

Time Frame: week 6

Upper limb symptoms and functional limitations were assessed using the Disability of the Arm Shoulder and Hand (DASH) questionnaire. DASH has 30 items that measures upper limb physical disability and symptoms. Final scores range from 0 to 100 (most severe disability).

Secondary Outcomes

  • Ultrasonographic measurements of acromiohumeral distance (AHD)(week 6)
  • Symptoms and functional limitations - Shoulder(week 6)

Study Sites (1)

Loading locations...

Similar Trials