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Clinical Trials/RBR-5pg989
RBR-5pg989
Recruiting
未知

Assessment and intervention of shoulder Dysfunction

niversidade Federal do Triângulo Mineiro0 sitesJuly 25, 2018

Overview

Phase
未知
Intervention
Not specified
Conditions
Shoulder
Sponsor
niversidade Federal do Triângulo Mineiro
Status
Recruiting
Last Updated
2 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
July 25, 2018
End Date
TBD
Last Updated
2 years ago
Study Type
Intervention

Investigators

Sponsor
niversidade Federal do Triângulo Mineiro

Eligibility Criteria

Inclusion Criteria

  • Category 1 volunteers will be included, adults 18 and older, of both sexes; patients with shoulder pain associated with range of motion limitation; we will not include patients diagnosed with cervical hernia, cervical stenosis, cervical spine degenerative diseases, cervical spine arthrodesis and Benign Paroxysmal Positional Vertigo; non\-athletes or regular physical activity practitioners who perform aerial launch movements; pregnant or reporting pregnancy will not be included; Acceptance in the Informed Consent Form.
  • Category 2 volunteers will be included, adults 18 and older, of both sexes; patients with shoulder pain associated with range of motion limitation; we will not include patients diagnosed with cervical hernia, cervical stenosis, cervical spine degenerative diseases, cervical spine arthrodesis and Benign Paroxysmal Positional Vertigo; athletes practicing regular physical activity that perform aerial launch movements; Acceptance in the Informed Consent Form.
  • Volunteers will be included for category 3, adults over 18 years of age, female; volunteers with complaints of wrist and hand pain with irradiation in the upper limb diagnosed as compressive syndrome will not include patients diagnosed with cervical hernia, cervical stenosis, cervical spine degenerative diseases, cervical spine arthrodesis and Benign Paroxysmal Positional Vertigo; non\-athletes or regular physical activity practitioners who perform aerial launch movements; pregnant or reporting pregnancy will not be included; Acceptance in the Informed Consent Form.

Exclusion Criteria

  • Participants who do not attend the reevaluations, do not carry out the proposed home protocol will be excluded; failure to complete the questionnaires; unable to perform the proposed exercises on the first day of the assessment; discomfort during the performance of exercises such as dizziness and nausea.

Outcomes

Primary Outcomes

Not specified

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