ACR Meeting Abstracts

ACR Meeting Abstracts

  • Meetings
    • ACR Convergence 2024
    • ACR Convergence 2023
    • 2023 ACR/ARP PRSYM
    • ACR Convergence 2022
    • ACR Convergence 2021
    • ACR Convergence 2020
    • 2020 ACR/ARP PRSYM
    • 2019 ACR/ARP Annual Meeting
    • 2018-2009 Meetings
    • Download Abstracts
  • Keyword Index
  • Advanced Search
  • Your Favorites
    • Favorites
    • Login
    • View and print all favorites
    • Clear all your favorites
  • ACR Meetings

Abstract Number: 833

Effect of a Mobile App to Monitor Patient Reported Outcomes in Rheumatoid Arthritis: A Randomized Controlled Trial

Yvonne Lee1, Fengxin Lu 2, Joshua Colls 2, Meredith Murray 2, Dong Suh 2, Jing Song 3, Julia (Jungwha) Lee 4, Dorothy Dunlop 4 and Daniel Solomon 5, 1Northwestern University Feinberg School of Medicine, Chicago, 2Brigham and Women's Hospital, Boston, MA, 3Northwestern University Feinberg School of Medicine, Worthington, OH, 4Northwestern University Feinberg School of Medicine, Chicago, IL, 5Brigham and Women´s Hospital, Div. of Rheumatology, Immunology and Allergy, Boston, MA

Meeting: 2019 ACR/ARP Annual Meeting

Keywords: Patient Satisfaction and Disease Activity, patient-reported outcome measures, Rheumatoid arthritis (RA)

  • Tweet
  • Click to email a link to a friend (Opens in new window) Email
  • Click to print (Opens in new window) Print
Session Information

Date: Sunday, November 10, 2019

Title: 3S076: Patient Outcomes, Preferences, & Attitudes I: Patient Reported Outcomes (833–838)

Session Type: ACR Abstract Session

Session Time: 2:30PM-4:00PM

Background/Purpose: Treat to target (TTT) is an effective strategy to improve outcomes in rheumatoid arthritis (RA). However, barriers to TTT include frequent clinic visits, poor access to rheumatologists, and poor patient acceptance of treatment escalation. Mobile technology may provide a solution by enabling collection of patient-reported outcomes (PROs) between clinic visits. The objectives of this study were to examine the effects of a mobile application (app) to monitor PROs on: 1) patient satisfaction and 2) disease activity in RA.

Methods: We conducted a 6-month randomized controlled trial of an app + population manager vs. population manager alone in 191 RA patients. Participants in the app group were prompted to answer daily questionnaires on disease activity, function, pain, fatigue, sleep, and mood, using an app. Both groups were assigned a population manager who spoke with participants on the telephone at 6 and 18 weeks. Population managers also communicated with participants in the app group if responses to the daily assessments indicated a sustained increase in disease activity. The analysis followed an intent-to-treat principle. Missing data were imputed using last observation carried forward. To address the aim of improving patient satisfaction, the main outcomes were the global satisfaction score from the Treatment Satisfaction Questionnaire for Medication (TSQM) and the Perceived Efficacy in Patient-Physician Interactions (PEPPI) score. To address the aim of decreasing disease activity, the primary outcome was the Clinical Disease Activity Index (CDAI). Treatment effects were estimated with repeated measures analyses (baseline, 3-month, 6-month), using bootstrapped quantile regression models, adjusted for age, sex, and race.

Results: Of the 191 participants, 156 (82%) were women. 29% were at least 65 years old. Baseline global TSQM and PEPPI scores were high, with a median of 83.3 (interquartile range [IQR] 66.7-100) and 50 (IQR 47-50), respectively ( Table ). The median baseline CDAI was 8 (IQR 4-14), indicating low disease activity. After 6 months, median TSQM scores were 83.3 (IQR 66.7-100) in both groups, and median PEPPI scores were 50 (IQR 47-50) in the app group and 50 (IQR 48-50) in the no app group ( Figure ). Median 6-month CDAI scores were 8 (IQR 4-14) in the app group vs. 10 (IQR 3-16) in the no app group. Quantile regression analyses indicated no group (app vs. no app) differences at 6-months in medians of: TSQM β 0.00, 95% confidence interval [CI] -9.18, 9.18; PEPPI β 0.00, 95% CI -0.16, 0.16; and CDAI β -0.50, 95% CI -3.82, 2.82. Adherence with the app was over 75% during the 6-month follow-up.

Conclusion: A mobile app designed to collect PRO data on RA symptoms did not improve patient satisfaction or disease activity. However, baseline satisfaction scores were high and disease activity was low, suggesting ceiling and floor effects. Adherence with the app was strong.  Future studies are needed to determine: a) if the app would be beneficial in a population with lower baseline satisfaction and/or more disease activity, and b) if improvements in the app (e.g., voice-enabled system, personalized frequency of data collection) would enhance efficacy.


Disclosure: Y. Lee, Cigna Corp, 1, Eli Lilly, 2, 5, Eli Lilly and Company, 2, Express Scripts, 4, Pfizer, 2; F. Lu, None; J. Colls, None; M. Murray, None; D. Suh, None; J. Song, None; J. Lee, None; D. Dunlop, None; D. Solomon, AbbVie, 2, Abbvie, 2, Amgen, 2, AstraZeneca, 2, Corrona, 2, Genentech, 2, Janssen, 2, Lilly, 2, Pfizer, 2.

To cite this abstract in AMA style:

Lee Y, Lu F, Colls J, Murray M, Suh D, Song J, Lee J, Dunlop D, Solomon D. Effect of a Mobile App to Monitor Patient Reported Outcomes in Rheumatoid Arthritis: A Randomized Controlled Trial [abstract]. Arthritis Rheumatol. 2019; 71 (suppl 10). https://acrabstracts.org/abstract/effect-of-a-mobile-app-to-monitor-patient-reported-outcomes-in-rheumatoid-arthritis-a-randomized-controlled-trial/. Accessed .
  • Tweet
  • Click to email a link to a friend (Opens in new window) Email
  • Click to print (Opens in new window) Print

« Back to 2019 ACR/ARP Annual Meeting

ACR Meeting Abstracts - https://acrabstracts.org/abstract/effect-of-a-mobile-app-to-monitor-patient-reported-outcomes-in-rheumatoid-arthritis-a-randomized-controlled-trial/

Advanced Search

Your Favorites

You can save and print a list of your favorite abstracts during your browser session by clicking the “Favorite” button at the bottom of any abstract. View your favorites »

All abstracts accepted to ACR Convergence are under media embargo once the ACR has notified presenters of their abstract’s acceptance. They may be presented at other meetings or published as manuscripts after this time but should not be discussed in non-scholarly venues or outlets. The following embargo policies are strictly enforced by the ACR.

Accepted abstracts are made available to the public online in advance of the meeting and are published in a special online supplement of our scientific journal, Arthritis & Rheumatology. Information contained in those abstracts may not be released until the abstracts appear online. In an exception to the media embargo, academic institutions, private organizations, and companies with products whose value may be influenced by information contained in an abstract may issue a press release to coincide with the availability of an ACR abstract on the ACR website. However, the ACR continues to require that information that goes beyond that contained in the abstract (e.g., discussion of the abstract done as part of editorial news coverage) is under media embargo until 10:00 AM ET on November 14, 2024. Journalists with access to embargoed information cannot release articles or editorial news coverage before this time. Editorial news coverage is considered original articles/videos developed by employed journalists to report facts, commentary, and subject matter expert quotes in a narrative form using a variety of sources (e.g., research, announcements, press releases, events, etc.).

Violation of this policy may result in the abstract being withdrawn from the meeting and other measures deemed appropriate. Authors are responsible for notifying colleagues, institutions, communications firms, and all other stakeholders related to the development or promotion of the abstract about this policy. If you have questions about the ACR abstract embargo policy, please contact ACR abstracts staff at [email protected].

Wiley

  • Online Journal
  • Privacy Policy
  • Permissions Policies
  • Cookie Preferences

© Copyright 2025 American College of Rheumatology