Relationship of Patient-Specific Functional Scale With Shoulder Functions: A Prospective Study
NCT ID: NCT04538118
Last Updated: 2020-09-07
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
36 participants
OBSERVATIONAL
2019-01-05
2019-05-25
Brief Summary
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Detailed Description
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Conditions
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Study Design
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COHORT
PROSPECTIVE
Study Groups
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Patient with a shoulder problem
Patients with shoulder problems between 18-65 years of age and being volunteered
Shoulder disability
Shoulder disability was evaluated with Patient-specific functional scale, the disabilities of the shoulder, arm and hand questionnaire, and the upper extremity functional index.
First assessment was applied when patients came to physical therapy clinic at first.
Second assessment was repeated after 6 weeks.
Shoulder Range of Motion
Shoulder range of motion was evaluated with universal goniometer. First assessment was applied when patients came to physical therapy clinic at first.
Second assessment was repeated after 6 weeks.
Pain Intensity
Pain intensity was evaluated with Numeric Pain Rating Scale. First assessment was applied when patients came to physical therapy clinic at first.
Second assessment was repeated after 6 weeks.
Interventions
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Shoulder disability
Shoulder disability was evaluated with Patient-specific functional scale, the disabilities of the shoulder, arm and hand questionnaire, and the upper extremity functional index.
First assessment was applied when patients came to physical therapy clinic at first.
Second assessment was repeated after 6 weeks.
Shoulder Range of Motion
Shoulder range of motion was evaluated with universal goniometer. First assessment was applied when patients came to physical therapy clinic at first.
Second assessment was repeated after 6 weeks.
Pain Intensity
Pain intensity was evaluated with Numeric Pain Rating Scale. First assessment was applied when patients came to physical therapy clinic at first.
Second assessment was repeated after 6 weeks.
Eligibility Criteria
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Inclusion Criteria
* being volunteer
* having shoulder pain at least 3 months
* being literate
Exclusion Criteria
* having an upper extremity pathology involving the neck and trunk
* having a neurological finding
18 Years
65 Years
ALL
No
Sponsors
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Ankara Yildirim Beyazıt University
OTHER
Responsible Party
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Principal Investigators
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Hidayet Cuha, MSc
Role: STUDY_CHAIR
Ankara Yildirim Beyazıt University
Locations
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Ankara Yıldırım Beyazıt University
Ankara, , Turkey (Türkiye)
Countries
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Other Identifiers
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363-37
Identifier Type: -
Identifier Source: org_study_id
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