Preferences and Insights for Participation in a Rheumatoid Arthritis Clinical Prevention Trial: A Mixed‐Methods Study. Issue 11 (16th September 2022)

• Record Type: Journal Article
• Authors: Fleischer, Chelsie L.; Bemis, Elizabeth A.; Feser, Marie L.; Kormendi, Vasilisa A.; Zhang, Alvina; Ketcham, Katherine; White, Sharon D.; Striebich, Christopher C.; Deane, Kevin D.; Harrison, Mark
• Is Part Of: ACR open rheumatology. Volume 4:Issue 11(2022)
• Page Start: 974
• Page End: 982
• Publication Date: 2022-09-16
• Subjects: Rheumatology -- Periodicals; 616.723005
• DOI: 10.1002/acr2.11500
• Languages: English
• ISSNs: 2578-5745

Abstract

Abstract : Objective: In rheumatoid arthritis (RA), anti–citrullinated protein antibodies (ACPA) can be elevated prior to inflammatory arthritis (IA). The potential to intervene in people with ACPA positivity underpins the development of prevention trials in RA. The Research Participation Influences Study examined factors influencing the decisions of individuals who are ACPA(+) to participate in a prevention trial using qualitative and quantitative methods. Methods: Individuals with ACPA positivity without IA were provided information regarding their risk for future RA, were provided a description of a clinical prevention trial using hydroxychloroquine, and were asked if they would participate in the trial. After agreeing to or declining participation, they were surveyed on what influenced their decision using Likert scales and open‐response questions. Results: Thirty‐nine individuals who agreed to trial participation (enrollees) and 31 individuals who declined (nonenrollees) completed surveys. Enrollees expressed greater perceived risk for RA and greater perception of benefit to themselves or others than nonenrollees. Nonenrollees expressed greater concern about medication effects and less personal or family experience with RA than enrollees. There was a higher proportion of first‐degree relatives (FDRs) of people with RA in enrollees versus nonenrollees (54% vs. 23%, P = 0.01). Conclusion: Enrollees were more likely than nonenrollees to be FDRs, exhibit stronger concern for personal risk for RA, and have less concern about adverse effects. Further exploration is needed to determine why these differences were present, including exploration of symptoms and the role of family history. Understanding these issues will better inform researchers and individuals who are candidates for prevention.