NCT01090271

Brief 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).

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
25

participants targeted

Target at below P25 for not_applicable

Timeline
Completed

Started Oct 2007

Shorter than P25 for not_applicable

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

Study Start

First participant enrolled

October 1, 2007

Completed
8 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

June 1, 2008

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

June 1, 2008

Completed
1.8 years until next milestone

First Submitted

Initial submission to the registry

March 18, 2010

Completed
1 day until next milestone

First Posted

Study publicly available on registry

March 19, 2010

Completed
Last Updated

March 19, 2010

Status Verified

September 1, 2007

Enrollment Period

8 months

First QC Date

March 18, 2010

Last Update Submit

March 18, 2010

Conditions

Shoulder Impingement Syndrome

Keywords

Subacromial impingement syndromeMuscle StrengthResistance Training

Outcome Measures

Primary Outcomes (1)

  • Isokinetic evaluation

    2 months

Secondary Outcomes (1)

  • Disabilities of the Arm, Shoulder, and Hand (DASH) questionnaire

    2 months

Study Arms (1)

Eccentric training

EXPERIMENTAL
Device: Isokinetic eccentric training

Interventions

Isokinetic eccentric trainingDEVICE

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

Eccentric training

Eligibility Criteria

Age18 Years - 60 Years
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64)

You may qualify if:

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

You may not qualify if:

  • 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

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Universidade Federal de Sao Carlos

São Carlos, São Paulo, 13565-905, Brazil

Location

MeSH Terms

Conditions

Shoulder Impingement Syndrome

Condition Hierarchy (Ancestors)

Joint DiseasesMusculoskeletal DiseasesShoulder InjuriesWounds and Injuries

Study Officials

  • Tânia TS Salvini, PhD

    Universidade Federal de Sao Carlos (Sao Paulo - Brazil)

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
interventional
Phase
not applicable
Allocation
NON RANDOMIZED
Masking
SINGLE
Who Masked
OUTCOMES ASSESSOR
Purpose
TREATMENT
Intervention Model
SINGLE GROUP
Sponsor Type
OTHER

Study Record Dates

First Submitted

March 18, 2010

First Posted

March 19, 2010

Study Start

October 1, 2007

Primary Completion

June 1, 2008

Study Completion

June 1, 2008

Last Updated

March 19, 2010

Record last verified: 2007-09

Locations

BR(1)