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SF-QUALIVEEN Turkish Validity and Reliability Study

Multiple Sclerosis Clinical Trial

Official title:
SF-QUALIVEEN Turkish Cultural Adaptation, Validity and Reliability Study

Clinical Trial Summary

Urological dysfunction is common in patients with Multiple Sclerosis (MS) and its prevalence has been reported at a high rate of 32-97%. Bladder dysfunction is associated with a significant deterioration in the quality of life of people with MS. In chronic diseases such as MS, patients experiences need to be measured directly in order to have information about patients perceptions about the effect of the disease on quality of life. However, there are a small number of valid and reliable Turkish scales on this subject.SF-Qualiveen is a validated scale for patients with MS who assess the urinary-specific quality of life by examining the impact of a wide range of bladder problems.The aim of our study is to make the Turkish cultural adaptation, validity and reliability of the SF-Qualiveen scale.

Clinical Trial Description

The aim of this study is to reveal the Turkish cultural adaptation, validity and reliability of the SF-Qualiveen scale. In our study, Sf-Qualiveen and Urogenital Distress Inventory (UDI-6) scales will be used. Pre-testing will be done in 10 patients with multiple sclerosis.Then, the validity and reliability of the scale will be performed in 80 patients with multiple sclerosis. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT04483609
Study type Observational
Source Istanbul Aydin University
Contact
Status Completed
Phase
Start date July 30, 2020
Completion date October 30, 2020
View Details
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