Shoulder
Conditions
Interventions
It will be a prospective, controlled, randomized, double-blind clinical trial, including volunteers with complaint of shoulder pain
Athletes complaining of shoulder pain
and volunteers diagnosed with Carpal Tunnel Syndrome. Volunteers from each category of the study will be divided into two groups, Intervention Group and Control Group. Each category will be divided in
Other
Sponsors
Universidade Federal do Triângulo Mineiro
Universidade Federal do Triângulo Mineiro
Eligibility
Age
18 Years to 60 Years
Inclusion 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
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.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| As a primary outcome or direct outcome pain relief of the selected volunteers for the study evaluated by the visual analog pain scale after the treatment protocol is expected. | — |
Secondary
| Measure | Time frame |
|---|---|
| As a secondary endpoint, we expect to gain range of motion and functional improvement of the affected limb that will be identified in the physical evaluation and through questionnaires before and after the treatment protocol. | — |
Countries
Brazil
Contacts
Public ContactLuciane Martinho Fernandes
Universidade Federal do Triângulo Mineiro
Outcome results
None listed