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The Reliability and Validity of the Turkish Version of the LSQ

Completed
Conditions
Lipedema
Women
Registration Number
NCT07061808
Lead Sponsor
Gazi University
Brief Summary

Abstract Background/ Aim: The aim of this study was to investigate the reliability and validity of the Turkish version of the Lipedema Screening Questionnaire (T-LSQ). Method: The study involved 59 female volunteers diagnosed with lipedema by a cardiovascular surgeon. Key demographics such as age, onset age, lipedema types and stages, clinical features, and BMI were recorded. The Turkish adaptation of the LSQ was performed in accordance with the protocol of Beaton. Confirmatory factor analysis was performed for structural validity. For concurrent validity, T- LSQ, the Lower Extremity Functional Scale (LEFS), the Lymphedema Life Impact Scale (LLIS), and the Lymphoedema Functioning, Disability and Health Quastionnaire for Lower Extremity Lymphedema (Lymph-ICF-LL) were applied and the correlation between the scale responses was analyzed. Test-retest and internal consistency reliability were performed.

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
Female
Target Recruitment
59
Inclusion Criteria
  • 18 years of age or older
  • had no communication cognitive and mental problem
  • participant in Turkish
Exclusion Criteria
  • Patients with diagnoses of renal and heart failure
  • individuals with history of lower extremity surgery
  • individuals with severe arterial venous disease involving the lower extremity
  • individuals with active cancer disease or metastasis
  • individuals with severe acute infective disease

Study & Design

Study Type
OBSERVATIONAL
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
The Validity and Reliability of Turkish version of the Lipedema Screening Questionnaireat 10-day intervals.

The Validity and Reliability of Turkish version of the Lipedema Screening Questionnaire: For validity, T-LSQ, Lower Extremity Functional Scale (LEFS), Lymphedema Life Impact Scale (LLIS) and Lymphedema Function, Disability and Health Questionnaire for Lower Extremity Lymphedema (Lymph-ICF-LL) were applied and correlation analysis between scale responses will be done. The LSQ questionnaire, whose reliability we measured, was applied at the beginning of the study and again after 10 days.

Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

aDepartment of Physiotherapy and Rehabilitation, Health Science Faculty, Gazi University, Ankara, Turkey

🇹🇷

Ankara, Turkey

aDepartment of Physiotherapy and Rehabilitation, Health Science Faculty, Gazi University, Ankara, Turkey
🇹🇷Ankara, Turkey

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