Ireland
--:--IST
Recruiting Observational

Turkish Validation of the Rapprich Lipedema Symptomatic Assessment Questionnaire

NCT07725146 · tracked via the Priya Life Science Turkey tracker
Phase
Observational
Started
2026-07-17
Last updated
2026-07-24

Condition(s) studied

Lipedema

Investigational drug(s) / intervention(s)

QuestionnairesPhysical Examination and Functional Testing

Questionnaires: Turkish version of Rapprich Lipedema Symptomatic Assessment Questionnaire: A 15-item scale used to evaluate the severity of lipedema symptoms (such as pain, tension, tenderness, bruising, and heaviness) on a 0-10 point rating scale. Short Form-36 (SF-36) Health Survey: A widely used, validated scale to assess the general health status and quality of life across eight sub-dimensions, used in this study for criterion validity

Physical Examination and Functional Testing: * Anthropometric and Vital Measurements: Recording of demographic data (age, height, weight, BMI), as well as arterial blood pressure and pulse rate. * Lipedema-Specific Assessment: Clinical determination of the lipedema stage (Stages I-III) and type (Types I-V). * Morphometric Measurements: Measurement of waist and hip circumferences (for waist-to-hip ratio) and actual leg length. * Lower Extremity Volume Calculation: Circular circumference measurements taken at 4 cm intervals starting from the ankle to calculate the total volume of both lower extremities. * 6-Minute Walk Test (6MWT): A functional test to evaluate the total walking distance and heart rate response, assessing the patient's functional capacity.

Study summary

Lipedema is a chronic disease characterized by abnormal fat accumulation, primarily in the lower extremities, affecting women. This study aims to evaluate the validity and reliability of the Turkish version of the Rapprich Lipedema Symptomatic Assessment Questionnaire, which was originally developed by Rapprich et al. in 2010. Since a validated Turkish version is currently unavailable, this research will provide a standardized tool for clinicians to assess symptomatic severity in Turkish-speaking lipedema patients.

Eligibility

Sex
FEMALE
Min age
18 Years
Max age
75 Years
Healthy volunteers
No
Inclusion Criteria: * Female patients aged 18-75. * Diagnosed with lipedema by a clinician. * Willingness to participate and sign the informed consent form. Exclusion Criteria: * Positive Stemmer sign or presence of advanced-stage lymphedema. * Diagnosis of Heart Failure. * Chronic Kidney Disease. * Pregnancy. * BMI \> 50 kg/m².

Primary outcome measure(s)

  • Internal Consistency (Cronbach's Alpha) — At baseline (Day 0).
    Evaluation of the internal consistency of the 15-item Turkish Rapprich Lipedema Questionnaire.

Trial sites (2)

FacilityCityRegionStatus
Sultan 2. Abdülhamid Han Training and Research Hospital, Physical Medicine and Rehabilitation Clinic, Istanbul, Turkey. Istanbul Kadıköy Recruiting
Marmara University Pendik Training and Research Hospital, Physical Medicine and Rehabilitation Department, Istanbul, Turkey. Istanbul Pendik Recruiting
Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07725146 on ClinicalTrials.gov ↗ ← All trials in Turkey