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Clinical Trials/NCT04409756
NCT04409756
Completed
Not Applicable

Validity and Reliability of the Turkish Version of the Shoulder Rating Questionnaire

Betül Tepeli1 site in 1 country122 target enrollmentDecember 1, 2018
ConditionsShoulder Pain

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Shoulder Pain
Sponsor
Betül Tepeli
Enrollment
122
Locations
1
Primary Endpoint
reliability of SRQ-T questionnaire
Status
Completed
Last Updated
5 years ago

Overview

Brief Summary

The purpose of this study is to determine the Turkish version of the Shoulder Rating Questionnaire (SRQ) and assign reliability and validity in Turkish patients.

Detailed Description

Shoulder pain is one of the common musculoskeletal disorders. A self- administered patient-based questionnaire has an important role for evaluate shoulder disabilities and also it is helpful for assess the treatment success.The purpose of this study is to determine the Turkish version of the Shoulder Rating Questionnaire (SRQ) and assign reliability and validity in Turkish patients.The Turkish version of the Shoulder Rating Questionnaire (SRQ-T) will be applied to patients after translation from English into Turkish. 122 patients will be participate to the study. Patients who were over 18 years with various shoulder pain complaints will be included into the study. The patients with mixed-type pain, cancer pain, headache, substance abuse, severe depression and fibromyalgia syndrome will be excluded. The musculoskeletal and neurological examinations of the patients will be performed. The Turkish version of the Shoulder Rating Questionnaire (SRQ-T) and Disabilities of arm, shoulder, hands-T (DASH-T) will be applied to all patients. SRQ-T and DASH-T will be collected in two sessions with at last three days between the sessions for pre-assessment and post-assessment. Reliability of SRQ-T questionnaire will be tested by internal consistency and test-retest reliability. Internal consistency will be evaluated by determining intraclass correlation coefficient (ICC) with 95% confidence interval, ranged between 0 and 1. To determine the internal consistency of the five domains of SRQ-T, Cronbach's alfa coefficient will be computed for both pre- and post-assessment of the questionnaire. The test-retest method with Wilcoxon Signed Rank Test will be used to determine reliability of SRQ-T and its domains. Then, Spearman correlation coefficients will be used to assess the discriminant validity of SRQ-T for evaluation of shoulder pain. The Spearman correlation coefficient score more than 0.70 will be accepted for reliability

Registry
clinicaltrials.gov
Start Date
December 1, 2018
End Date
March 1, 2019
Last Updated
5 years ago
Study Type
Interventional
Study Design
Single Group
Sex
All

Investigators

Sponsor
Betül Tepeli
Responsible Party
Sponsor Investigator
Principal Investigator

Betül Tepeli

Department of Physical Medicine And Rehabilitation, Private Balkan Hospital,Principal Investigator,

Namik Kemal University

Eligibility Criteria

Inclusion Criteria

  • Patients who were over 18 years with various shoulder pain complaints

Exclusion Criteria

  • The patients with mixed-type pain, cancer pain, headache, substance abuse, severe depression and fibromyalgia syndrome

Outcomes

Primary Outcomes

reliability of SRQ-T questionnaire

Time Frame: through study completion, an average of 1 month

Reliability of SRQ-T questionnaire will be tested by internal consistency and test-retest reliability. Internal consistency will be evaluated by determining intraclass correlation coefficient (ICC) with 95% confidence interval, ranged between 0 and 1.

Study Sites (1)

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