Skip to main content
OpenTrials
Completed

NCT Number: NCT02695524

Exercise Application in the Treatment of Patients With Subacromial Pain Syndrome

This study evaluate the effectiveness of adding neuromuscular exercises with tactile, visual and auditory feedback to a scapula-focused treatment, both emphasizing the periscapular muscles on improvement of disability in patients with subacromial pain syndrome compared to patients receiving only strengthening exercise protocol.

Completed

Looking for future studies?

Notify Me

Key information

Age range

18 year–60 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

University of São Paulo, Ribeirão Preto Medical School

Ribeirão Preto, São Paulo, 14049-900, Brazil

About this study

Evidence of the effectiveness conservative treatments in shoulder impingement are in favor the application of specific exercises for scapulothoracic muscles and rotator cuff on pain reduction and improvement of upper limb function, supervised or performed at home, and these same exercises associated with other therapies promote a greater reduction in pain and improvement in disability.

Currently, the evidence of better methodological quality present in the literature13 points out that the performance of motor control exercises focused on the scapula associated with mobilization and stretching generate pain improvement and clinically relevant improvement of the function. The few studies in this area have great methodological diversity with significant limitations. The hypothesis is that patients with subacromial pain syndrome who will receive traditional exercise protocol with the addition of neuromuscular training will show less functional disability, a greater reduction in pain intensity, increase muscle strength and range of motion when compared to the patient group that will receive only the protocol without neuromuscular training, immediately after the intervention, four and eight weeks and four months after randomization and that these benefits are clinically relevant.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Diagnosis of subacromial pain syndrome with confirmed positivity in at least three of the five specific orthopedic impact tests: Neer test, Hawkins- Kennedy test, painful arc, external rotation resistance and empty can. Present history of pain in the shoulder lasting more than a week located in the proximal area of the shoulder

Exclusion criteria

  • Subjects with a history of trauma or shoulder surgery, total rupture of the rotator cuff tendon and biceps, physically active involving the upper limbs or considered active accordance with the short version International Physical Activity Questionnaire (IPAQ). Subjects who have neurological diseases, referred pain in arms (indicative of involvement in the cervical or thoracic region), systemic disease involving the joints such as rheumatoid arthritis or fibromyalgia, the presence of disorders in the wrist such as carpal tunnel syndrome, and have done physical therapy in the shoulder the last six months.

Treatment and study plan

Scapula-focused exercises

Other

Motor control exercises

Other

Primary outcomes

  1. Change in Functionality Evaluated With Specific Questionnaire

    Time frame: baseline, four and eight weeks and sixteen weeks after randomization

    The Brazilian version of Shoulder Pain and Disability Index ranging 0 to 100 points. Lower scores indicate better functionality

Secondary outcomes

  1. Change in Intensity of Pain Evaluated by a Scale

    Time frame: baseline, four and eight weeks and sixteen weeks after randomization

    Pain Numerical Rating Scale from 0 to 10. Lower values indicate improvement in pain

  2. Change in Strength Evaluated by Hand Held Dynamometer and the Measures Provided in Kilogram-force (KgF)

    Time frame: baseline, four and eight weeks and sixteen weeks after randomization

    Strength of serratus anterior, trapezius muscles, abduction, adduction, internal and external rotation movements the arm with hand held Dynamometer.

  3. Perceived Change Evaluated by Numerical Scale

    Time frame: four, eight weeks and sixteen weeks of randomization

    Global Perceived Effect Scale ranging -5 to +5 points. Positive values indicate improvement and negative values indicate worsening of symptoms

  4. Change in Kinesiophobia Evaluated With Specific Questionnaire

    Time frame: baseline, four and eight weeks and sixteen weeks after randomization

    Tampa Scale of Kinesiophobia ranging 17 to 68 points. High scores indicate high degree kinesiophobia

  5. Range of Motion Evaluated by Digital Inclinometer and the Measures Provided in Degrees

    Time frame: baseline, four and eight weeks and sixteen weeks after randomization

    abduction, adduction, internal and external rotation of the shoulder

  6. Satisfaction With Treatment Evaluated With Specific Questionnaire

    Time frame: four, eight weeks and sixteen weeks after randomization

    Medrisk Questionnaire ranging 13 to 80 points. High scores indicate satisfaction with treatment

  7. Scapula Position Evaluated by Digital Inclinometer and the Measures Provided in Degrees

    Time frame: baseline, four and eight weeks and sixteen weeks after randomization

    upward rotation and tilt of the scapula

Sponsors and collaborators

Lead sponsor

University of Sao Paulo

Other

Registry information

Official study title

Effect of Scapula-focused Treatment With Additional Motor Control Exercises on Pain and Disability in Patients With Subacromial Pain Syndrome: A Randomized Controlled Trial

Important dates

Study start
2016
Primary completion
2017
Study completion
2017
First posted
Mar 1, 2016
Registry last updated
Aug 19, 2019

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Published trials that share one or more normalized conditions with this study.