<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>14(8)</volume><submitter>Bibeau K</submitter><funding>Incyte</funding><pubmed_abstract>&lt;h4>Introduction&lt;/h4>This study reports psychometric testing of the facial and total Vitiligo Area Scoring Index quantitative clinical instruments (F-VASI [range: 0-3], T-VASI [range: 0-100], respectively) using data from two phase 3 randomized, vehicle-controlled studies of ruxolitinib cream (TRuE-V1/TRuE-V2), the largest vitiligo trials conducted to date. Because VASI assessment is required by regulatory authorities, we evaluated the psychometric properties of the VASI instruments and confirmed thresholds for clinically meaningful change.&lt;h4>Methods&lt;/h4>The TRuE-V1/TRuE-V2 full analysis set population included 652 patients (≥ 12 years old with nonsegmental vitiligo affecting ≤ 10% total body surface area, F-VASI ≥ 0.5, and T-VASI ≥ 3 at baseline). Data collected using the facial and tota</pubmed_abstract><journal>Dermatology and therapy</journal><pagination>2223-2234</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC11333635</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Psychometric Evaluation of the Facial and Total Vitiligo Area Scoring Index Instruments in the TRuE-V Phase 3 Studies.</pubmed_title><pmcid>PMC11333635</pmcid><pubmed_authors>Wang M</pubmed_authors><pubmed_authors>Hamzavi IH</pubmed_authors><pubmed_authors>Skaltsa K</pubmed_authors><pubmed_authors>Butler K</pubmed_authors><pubmed_authors>Bibeau K</pubmed_authors></additional><is_claimable>false</is_claimable><name>Psychometric Evaluation of the Facial and Total Vitiligo Area Scoring Index Instruments in the TRuE-V Phase 3 Studies.</name><description>&lt;h4>Introduction&lt;/h4>This study reports psychometric testing of the facial and total Vitiligo Area Scoring Index quantitative clinical instruments (F-VASI [range: 0-3], T-VASI [range: 0-100], respectively) using data from two phase 3 randomized, vehicle-controlled studies of ruxolitinib cream (TRuE-V1/TRuE-V2), the largest vitiligo trials conducted to date. Because VASI assessment is required by regulatory authorities, we evaluated the psychometric properties of the VASI instruments and confirmed thresholds for clinically meaningful change.&lt;h4>Methods&lt;/h4>The TRuE-V1/TRuE-V2 full analysis set population included 652 patients (≥ 12 years old with nonsegmental vitiligo affecting ≤ 10% total body surface area, F-VASI ≥ 0.5, and T-VASI ≥ 3 at baseline). Data collected using the facial and tota</description><dates><release>2024-01-01T00:00:00Z</release><publication>2024 Aug</publication><modification>2026-06-02T04:47:29.18Z</modification><creation>2025-05-18T12:15:33.512Z</creation></dates><accession>S-EPMC11333635</accession><cross_references><pubmed>39078582</pubmed><doi>10.1007/s13555-024-01223-y</doi></cross_references></HashMap>