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Clinical Trials/RBR-8k98md3
RBR-8k98md3
Not yet recruiting
未知

Efficacy of adding Self-Efficacy Strategies to Strengthening Exercises and Manual Therapy for disability and self-efficacy of individuals with chronic shoulder pain: a randomized controlled trial with economic evaluation

Faculdade de Medicina de Ribeirão Preto - Universidade de São Paulo0 sitesJanuary 18, 2023

Overview

Phase
未知
Intervention
Not specified
Conditions
Subacromial Impingement Syndrome
Sponsor
Faculdade de Medicina de Ribeirão Preto - Universidade de São Paulo
Status
Not yet recruiting
Last Updated
2 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
January 18, 2023
End Date
August 1, 2025
Last Updated
2 years ago
Study Type
Intervention

Investigators

Sponsor
Faculdade de Medicina de Ribeirão Preto - Universidade de São Paulo

Eligibility Criteria

Inclusion Criteria

  • Individuals who have one of the following diagnostic terms Anterior shoulder pain”; Subacromial Impingement Syndrome”; Subacromial Impingement Syndrome”; Painful shoulder”; Shoulder Tendinitis” or specific rotator cuff tendonitis; Subacromial bursitis” or Subdeltoid bursitis” in the diagnostic field; Both sexes; Age from 18 years old; Shoulder pain for more than 12 weeks; 3 or more positive findings in the Painful arch in flexion or abduction” tests; Neer”; Hawkins\-Kennedy Test”; pain on resisted external humeral rotation” or Jobe's Test”

Exclusion Criteria

  • Previous history of shoulder surgery or injuries caused by external forces; full\-thickness tear of the rotator cuff as evidenced by imaging (US or MRI); shoulder instability; adhesive capsulitis; or if they are involved in cognitive\-behavioral and cognitive\-functional therapy due to conflicting literature on possible changes in self\-efficacy in this population; Cardiovascular and neurological disorders including cervical and arm nerve entrapment syndromes; pregnant women; those who are unable to perform the required clinical assessment tasks, answer the questionnaires, or attend the required assessment and intervention sessions

Outcomes

Primary Outcomes

Not specified

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