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Abstract Number: 1926

Effects of Social Networking on Chronic Disease Management in Rheumatoid Arthritis

Maria A. Lopez-Olivo1, Jessica Foreman2, Heather Lin3, Cheuk Hong Leung4, Tiffany Westrich-Robertson5, Catherine Hofstetter6, Susan K. Peterson7, Anne Lyddiatt8, Amye L. Leong9, Irmgard U. Willcockson10 and Maria Suarez-Almazor1, 1Section of Rheumatology and Clinical Immunology, Department of General Internal Medicine, The University of Texas MD Anderson Cancer Center, Houston, TX, 2Section of Rheumatology and Clinical Immunology, Department of General Internal Medicine, The University of Texas MD Anderson Cancer Center, Houston, Texas, USA, Houston, TX, 3Biostatistics, Department of Biostatistics, The University of Texas MD Anderson Cancer Center, Houston, TX, USA, Houston, TX, 4Department of Biostatistics, Department of Biostatistics, The University of Texas MD Anderson Cancer Center, Houston, TX, USA, Houston, TX, 5International Foundation for Autoimmune and Autoinflammatory Arthritis, Saint Louis, Missouri, USA, St Louis, MO, 6OMERACT patient research partner group, Ottawa, ON, Canada, 7Department of Behavioral Science, The University of Texas MD Anderson Cancer Center, Houston Texas, USA, Houston, TX, 8Musculoskeletal Group, Cochrane Collaboration, Hamilton, ON, Canada, 9Spokesperson; Strategic Relations, Bone and Joint Decade, Santa Barbara, CA, 10School of Biomedical Informatics, University of Texas Health Science Center at Houston, Houston, TX

Meeting: 2018 ACR/ARHP Annual Meeting

Keywords: online patient engagement, RCT, Rheumatoid arthritis (RA), social media and social support

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Session Information

Date: Monday, October 22, 2018

Title: 4M104 ACR Abstract: Patient Outcomes, Preferences, & Attitudes I: Beliefs & Behaviors (1923–1928)

Session Type: ACR Concurrent Abstract Session

Session Time: 4:30PM-6:00PM

Background/Purpose: We evaluated a social networking intervention to help patients with rheumatoid arthritis become active partners in their own care. We developed a closed independent community in Facebook® for patients with rheumatoid arthritis. Three patient advocates with expertise in health communication moderated the Facebook® community.

Methods: In a randomized controlled trial we compared the use of Facebook® as an educational platform providing evidence-based health information and social networking to a static non-participatory website offering the same educational materials as Facebook but without the interactive components of social networking (intervention = Facebook® + website and control = website alone). Inclusion criteria were: (i) adults diagnosed with rheumatoid arthritis by a rheumatologist, and ongoing or prior treatment with traditional disease-modifying antirheumatic drugs or biologic agents, (ii) able to communicate in English; (iii) internet access and a personal email account; (iv) current use of internet-based social media platforms (Facebook® or similar); and (v) disease duration ≤ 10 years. Our primary outcome measures were patients’ disease knowledge, self-efficacy and empowerment. Follow-up assessment were conducted at 3 and 6 months. Repeated measures ANOVA was used to compare the primary outcome measures between two study groups at 3-month and 6-month follow-up. All analyses were done on an intention-to-treat basis.

Results: 210 patients agreed to participate and completed the baseline questionnaire. After completion of the baseline questionnaire, participants were randomly assigned at 1:1 ratio; 105 were randomized to the intervention arm and 105 were randomized to the control arm. No statistically significant differences between the two study groups were detected at baseline. At the 3-month assessment, 90 patients from the intervention arm and 93 patients from the control arm completed the survey (87% response rate). At the 6-month assessment, 89 patients from the intervention arm and 89 patients from the control arm completed the survey (85% response rate). No statistically significant differences were observed between groups for patient knowledge, self-efficacy, or empowerment at 3 or 6 months. However, the intervention group reported more satisfaction with their perceived peer support compared with the control group at 3 and 6 months. This was reflected in the various subscales including perceived availability of peer support (i.e., peer supporter being present and ready to help), perceived assistance in daily management (i.e., peer supporter assistance in the actions needed to take every day to control the disease and protect the patients’ health), social & emotional support (i.e., peer supporter addressing the emotional aspects of living with rheumatoid arthritis), and linkage to clinical care (i.e., peer supporter helping to make effective use of health services).

Conclusion: The perceived receipt of direct and nondirective support was higher in patients using Facebook®, but this was not translated into greater knowledge, self-efficacy or empowerment.


Disclosure: M. A. Lopez-Olivo, None; J. Foreman, None; H. Lin, None; C. H. Leung, None; T. Westrich-Robertson, None; C. Hofstetter, None; S. K. Peterson, None; A. Lyddiatt, None; A. L. Leong, None; I. U. Willcockson, None; M. Suarez-Almazor, None.

To cite this abstract in AMA style:

Lopez-Olivo MA, Foreman J, Lin H, Leung CH, Westrich-Robertson T, Hofstetter C, Peterson SK, Lyddiatt A, Leong AL, Willcockson IU, Suarez-Almazor M. Effects of Social Networking on Chronic Disease Management in Rheumatoid Arthritis [abstract]. Arthritis Rheumatol. 2018; 70 (suppl 9). https://acrabstracts.org/abstract/effects-of-social-networking-on-chronic-disease-management-in-rheumatoid-arthritis/. Accessed .
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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.

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