Psychometric Evaluation of the Scleroderma Skin Questionnaire: A Novel Patient-Reported Outcome for Skin Disease in Patients With Systemic Sclerosis

Jeong Min Yu*, John M. VanBuren, Angela Child, Jessica S. Alvey, Lisa A. Mandl, Laura C. Pinheiro, Shervin Assassi, Elana J. Bernstein, Flavia V. Castelino, Lorinda Chung, Luke Evnin, Tracy M. Frech, Faye N. Hant, Laura K. Hummers, Dinesh Khanna, Kimberly S. Lakin, Dorota Lebiedz-Odrobina, Yiming Luo, Ashima Makol, Jerry A. MolitorDuncan F. Moore, Carrie Richardson, Nora Sandorfi, Ami A. Shah, Ankoor Shah, Victoria K. Shanmugam, Brian Skaug, Virginia D. Steen, Elizabeth R. Volkmann, Jessica K. Gordon

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

Abstract

Objective. We aimed to evaluate the psychometric properties of the Scleroderma Skin Questionnaire (SSQ), a novel patient-reported outcome (PRO) to assess systemic sclerosis (SSc)–related skin symptoms. Methods. Participants were recruited from the SSc Collaborative National Quality and Efficacy Registry (CONQUER). Internal consistency was determined using Cronbach α and McDonald ω total (ωt). The correlation of the SSQ was assessed with the modified Rodnan skin score (mRSS), physician global assessment (PGA), Scleroderma Health Assessment Questionnaire, 29-item Patient-Reported Outcomes Measurement Information System (PROMIS-29), and patient global assessment to assess criterion, convergent, and divergent validity. Correlations were also assessed between patients’ self-reported recall of skin changes over the past 6 months (“SSQ 6-Month”) and 6-month change in mRSS. Results. The SSQ was administered to 799 adults (mean age 52.7; 83% female) enrolled in CONQUER. Cronbach α was 0.90 and ωt was 0.92, indicating high internal consistency. The SSQ was moderately correlated with mRSS (r 0.56), with stronger correlations in diffuse (r 0.54) vs limited cutaneous subtypes (r 0.24; all P < 0.05). The SSQ was also moderately-to-strongly correlated with PROMIS-29 physical function (r –0.50) and pain interference subscales (r 0.61), strongly with Health Assessment Questionnaire score (r 0.63) and severity subscale (r 0.62), and moderately with PGA SSc activity score (r 0.48; all P < 0.05). SSQ 6-Month correlated weakly with the 6-month change in mRSS (r 0.26; P < 0.05). Conclusion. SSQ demonstrated high reliability and moderate correlation with mRSS and legacy PROs. This study provides initial support for SSQ, but not SSQ 6-Month, to assess skin symptoms in patients with SSc.

Original languageEnglish (US)
Pages (from-to)263-269
Number of pages7
JournalJournal of Rheumatology
Volume52
Issue number3
DOIs
StatePublished - Mar 1 2025

Funding

The work described in this manuscript was completed while JY was employed at The Hospital for Special Surgery. The opinions expressed in this article do not reflect the view of the US Food and Drug Administration, the Department of Health and Human Services, or the US government. The work described in this manuscript was completed while VDS was employed at The George Washington University Medical Faculty Associates. The opinions expressed in this article do not reflect the view of the National Institutes of Health, the Department of Health and Human Services, or the US government.

Keywords

  • outcome assessment
  • outcomes
  • registries
  • scleroderma
  • skin
  • systemic sclerosis

ASJC Scopus subject areas

  • Rheumatology
  • Immunology and Allergy
  • Immunology

Fingerprint

Dive into the research topics of 'Psychometric Evaluation of the Scleroderma Skin Questionnaire: A Novel Patient-Reported Outcome for Skin Disease in Patients With Systemic Sclerosis'. Together they form a unique fingerprint.

Cite this