ClinicalTrials.Veeva

Menu

Effects of Overload Progressive in the Treatment of Shoulder

U

University of Nove de Julho

Status

Completed

Conditions

Shoulder Impingement Syndrome

Treatments

Other: Strengthening protocol without progressive load
Other: Strengthening protocol with progressive load

Study type

Interventional

Funder types

Other

Identifiers

NCT02870257
1.487.198

Details and patient eligibility

About

Seventy subjects with shoulder impingement syndrome associated with scapular dyskinesis will be recruited and randomized into two groups of treatment. The group "a" will receive a strenghtening protocol with progressive overload during 20 sessions and group "b" will receive the same protocol with minimal load, without change during the 20 sessions. The primary outcomes measures will be pain, function, quality of life, global impression of recovery. The change will be measure from baseline at 10 weeks (after 20 sessions), 3 and 6 months (follow-up). The secundary outcomes will be disability, quality of life measure by other instruments, shoulder muscle strength and scapular 3d kinematic variables. For these data, change will be measure from baseline at 10 weeks (after 20 sessions).

Enrollment

70 patients

Sex

All

Ages

35 to 70 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • People with diagnosis shoulder impingement syndrome or supraspinatus/rotator cuff tendinopathy or subacromial bursitis
  • shoulder pain for more than 4 months, at least 4 points of pain in 0-10 NPRS
  • at least 130° shoulder active elevation
  • 3 or more positive of 5 physical examination tests (painful arc, external rotation resistence, Neer, empty can (Jobe) and Hawkins-Kennedy
  • positive dynamic scapular dyskinesis in clinical observation

Exclusion criteria

  • Referred pain from vertebral spine
  • previous shoulder, elbow or neck surgery
  • complete rotator cuff tear (positive drop arm sign or substantial shoulder elevation or rotation weakness)
  • neoplastic or neurological disorders
  • previous fracture or dislocation injury (shoulder, humerus, clavicle)
  • adhesive capsulitis signs
  • inflammatory diseases
  • specific treatment for the shoulder in the previous four months (injection, physiotherapy)
  • using drugs in the previous week
  • inability to understand portuguese language

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Double Blind

70 participants in 2 patient groups

Progressive overload strengthening group
Experimental group
Description:
Strengthening protocol with progressive load Strengthening muscle exercises for the shoulder and scapular with progressive increase of load during 10 weeks (20 sessions)
Treatment:
Other: Strengthening protocol with progressive load
Strengthening group
Active Comparator group
Description:
Strengthening protocol without progressive load Strengthening muscle exercises for the shoulder and scapular without increase of load (minimal load) during 10 weeks (20 sessions)
Treatment:
Other: Strengthening protocol without progressive load

Trial contacts and locations

1

Loading...

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2024 Veeva Systems