Ireland
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Recruiting Observational

Validity and Reliability of the Turkish Duke Activity Status Index in Women With Lipedema

NCT07803913 · tracked via the Priya Life Science Turkey tracker
Phase
Observational
Started
2026-08-25
Last updated
2026-09-10

Condition(s) studied

Lipedema

Investigational drug(s) / intervention(s)

Duke Activity Status Index (DASI)

Duke Activity Status Index (DASI): The Duke Activity Status Index (DASI) is a 12-item self-administered questionnaire used to assess functional capacity based on activities of daily living. The total score ranges from 0 to 58.2, with higher scores indicating better functional capacity. The Turkish version of the DASI will be administered at the initial assessment and repeated after 7 days to evaluate test-retest reliability.

Study summary

This study aims to evaluate the validity and reliability of the Turkish version of the Duke Activity Status Index (DASI) in women with lipedema. DASI is a 12-item questionnaire designed to assess functional capacity based on activities of daily living. The study will examine the test-retest reliability and internal consistency of the Turkish DASI and investigate its validity by examining its relationships with functional exercise capacity, lower extremity function, and health-related quality of life. The findings are expected to determine whether the Turkish DASI is a valid and reliable tool for assessing functional capacity in women with lipedema.

Eligibility

Sex
FEMALE
Min age
18 Years
Max age
65 Years
Healthy volunteers
No
Inclusion Criteria: * Female sex. * Aged 18 to \<65 years. * Diagnosis of lipedema. * No participation in a physiotherapy program within the previous 3 months. * No history of liposuction surgery. * Not currently following a weight-loss diet. * No change in body weight greater than 10% within the previous 6 months. * Willing to participate in the study and able to provide informed consent. Exclusion Criteria: * Severe visual or cognitive impairment. * Severe cardiovascular disease. * Musculoskeletal disorders or injuries affecting the lower extremities, including osteoarthritis, contracture, or osteoporosis, that may interfere with study assessments. * Skin conditions that may interfere with the assessments, such as pressure ulcers. * Uncontrolled endocrine disorders, including type 1 or type 2 diabetes mellitus or hypothyroidism. * Obesity secondary to endocrine disorders or medication-induced obesity. * Use of estrogen-progestin therapy within the previous 2 months. * Pregnancy or a positive pregnancy test. * Breastfeeding. * Concurrent participation in another clinical trial.

Primary outcome measure(s)

  • Test-Retest Reliability of the Turkish Duke Activity Status Index — Baseline and 7 days
    Test-retest reliability of the Turkish version of the Duke Activity Status Index (DASI) will be evaluated by administering the questionnaire twice, with a 7-day interval. The DASI consists of 12 items assessing functional capacity during activities of daily living, with a total score ranging from 0 to 58.2; higher scores indicate better functional capacity. Test-retest reliability will be assessed using the intraclass correlation coefficient (ICC).
  • Construct Validity of the Turkish Duke Activity Status Index — Baseline-7 days
    Construct validity of the Turkish DASI will be evaluated by examining the relationships between DASI scores and the Six-Minute Walk Test (6MWT), Lower Extremity Functional Scale (LEFS), and 36-Item Short Form Health Survey (SF-36). Correlation analyses will be used to determine the strength and direction of the relationships between these measures.

Trial sites (1)

FacilityCityRegionStatus
Bezmialem Vakif University Istanbul Eyupsultan 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 NCT07803913 on ClinicalTrials.gov ↗ ← All trials in Turkey