Evaluation of Functional Status, Physical Activity and Quality of Life in Patients With Rotator Cuff Syndrome

Study Results

Results pending

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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Recruitment Status

COMPLETED

Total Enrollment

40 participants

Study Classification

OBSERVATIONAL

Study Start Date

2015-03-25

Study Completion Date

2016-12-22

Brief Summary

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Pain is one of the most important factors affecting the quality of life. The quality of life of patients with pain and restricted shoulder movements can be affected in patients with Rotator Cuff Syndrome (RCS).

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Detailed Description

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The aim of our study is to examine the effect of the pain on functional status, quality of life and physical activity levels in daily life activities of RCS patients.

Conditions

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Rotator Cuff Syndrome

Study Design

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Observational Model Type

CASE_ONLY

Study Time Perspective

OTHER

Study Groups

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Evaluation tests

RCS cases between the ages of 19-64 (n:40) who agreed to participate were included in the study. Pain severity (Visual Analogue Scale - VAS), range of motion (Universal Goniometer), muscle test (Manual muscle test), upper extremity functional status and disability (Quick-DASH questionnaire), physical activity level (International Physical Activity Questionnaire - UFAA) ) and quality of life (Short Form-36 - SF-36) were evaluated

Quality of life and daily living activities assessment tests

Intervention Type OTHER

Interventions

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Quality of life and daily living activities assessment tests

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

* Patients presenting with shoulder pain problems and diagnosed with RCS.
* Individuals between the ages of 19-64 were included in the study.

Exclusion Criteria

* Those who have mental disability at the level of understanding the test and preventing interviews.
* Those with any chronic problems (such as cancer, kidney failure)
* Those who receive special medical treatment (steroid therapy, chemotherapy, insulin use.)
* Those who had a pregnancy status were excluded from the study.

Minimum Eligible Age

19 Years

Maximum Eligible Age

64 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes