University of São Paulo, Ribeirão Preto Medical School
Ribeirão Preto, São Paulo, 14049-900, Brazil
NCT Number: NCT02695524
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.
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Notify Me18 year–60 year
All sexes
Interventional
Not applicable
Ribeirão Preto, São Paulo, 14049-900, Brazil
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.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
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
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
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.
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
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
Time frame: baseline, four and eight weeks and sixteen weeks after randomization
abduction, adduction, internal and external rotation of the shoulder
Time frame: four, eight weeks and sixteen weeks after randomization
Medrisk Questionnaire ranging 13 to 80 points. High scores indicate satisfaction with treatment
Time frame: baseline, four and eight weeks and sixteen weeks after randomization
upward rotation and tilt of the scapula
University of Sao Paulo
Other
Effect of Scapula-focused Treatment With Additional Motor Control Exercises on Pain and Disability in Patients With Subacromial Pain Syndrome: A Randomized Controlled Trial
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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.
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