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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01090271
Other study ID # UFSCar-214/2007
Secondary ID
Status Completed
Phase N/A
First received March 18, 2010
Last updated March 18, 2010
Start date October 2007
Est. completion date June 2008

Study information

Verified date September 2007
Source Universidade Federal de Sao Carlos
Contact n/a
Is FDA regulated No
Health authority Brazil: Ethics Committee
Study type Interventional

Clinical Trial Summary

The aim of the study was to evaluate the effect of eccentric strength training for shoulder abductors on force steadiness in subjects with subacromial impingement syndrome (SIS).


Description:

Although it is known that shoulder abduction in subjects with subacromial impingement syndrome (SIS) presents alterations in several parameters, as for example, in scapular and glenohumeral kinematics, the strengthening of the shoulder abductors as an intervention strategy is controversial in literature.

Strength training has been shown to be effective in reducing the fluctuations in force and had a positive effect on isometric steadiness in old adults and in healthy young subjects during bed rest. However, there are no studies that evaluated the effects of strength training on the force steadiness in subjects with SIS.


Recruitment information / eligibility

Status Completed
Enrollment 25
Est. completion date June 2008
Est. primary completion date June 2008
Accepts healthy volunteers No
Gender Both
Age group 18 Years to 60 Years
Eligibility Inclusion Criteria:

- subjects diagnosed with Subacromial impingement syndrome by a physical therapist (the diagnosis was confirmed by an orthopaedic physician).

Exclusion Criteria:

- pregnancy

- torn rotator cuff or long head biceps tendons

- ligamentous laxity based on positive Sulcus test or a positive apprehension test

- previous shoulder or neck surgery

- hooked acromion

- systemic illnesses

- corticosteroid injection 3 months prior to evaluation

- physical therapy 6 months prior to evaluation

Study Design

Allocation: Non-Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Single Group Assignment, Masking: Single Blind (Outcomes Assessor), Primary Purpose: Treatment


Related Conditions & MeSH terms


Intervention

Device:
Isokinetic eccentric training
The eccentric training for the shoulder abductors was performed for 6 consecutive weeks, twice a week, on alternate days.

Locations

Country Name City State
Brazil Universidade Federal de Sao Carlos Sao Carlos Sao Paulo

Sponsors (2)

Lead Sponsor Collaborator
Universidade Federal de Sao Carlos Coordenaçao de Aperfeiçoamento de Pessoal de Nível Superior

Country where clinical trial is conducted

Brazil, 

Outcome

Type Measure Description Time frame Safety issue
Primary Isokinetic evaluation 2 months Yes
Secondary Disabilities of the Arm, Shoulder, and Hand (DASH) questionnaire 2 months Yes
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