Volume 132, Issue 9 pp. 1835-1842
Original Reports

An Exploration of Online Support Community Participation Among Patients With Vestibular Disorders

Erik B. Vanstrum BA

Erik B. Vanstrum BA

Keck School of Medicine, University of Southern California, Los Angeles, California, U.S.A.

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Joni K. Doherty MD, PhD

Joni K. Doherty MD, PhD

Caruso Department of Otolaryngology – Head and Neck Surgery, University of Southern California, Los Angeles, California, U.S.A.

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Uttam K. Sinha MD

Uttam K. Sinha MD

Caruso Department of Otolaryngology – Head and Neck Surgery, University of Southern California, Los Angeles, California, U.S.A.

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Courtney C. J. Voelker MD, PhD

Courtney C. J. Voelker MD, PhD

Caruso Department of Otolaryngology – Head and Neck Surgery, University of Southern California, Los Angeles, California, U.S.A.

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Alaina M. Bassett AuD, PhD

Corresponding Author

Alaina M. Bassett AuD, PhD

Caruso Department of Otolaryngology – Head and Neck Surgery, University of Southern California, Los Angeles, California, U.S.A.

Send correspondence to Alaina M. Bassett, 1640 Marengo St. Los Angeles, CA 90033. E-mail: [email protected]

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First published: 10 December 2021
Citations: 3

Editor's Note: This Manuscript was accepted for publication on November 26, 2021.

The authors have no funding, financial relationships, or conflicts of interest to disclose.

Abstract

Objectives/Hypothesis

To formally document online support community (OSC) use among patients with vestibular symptoms and gain an appreciation for the perceived influence of participation on psychosocial outcomes and the impact on medical decision-making.

Study Design

Self reported internet-based questionnaire.

Methods

The Facebook search function was paired with a comprehensive list of vestibular diagnoses to systematically collect publicly available information on vestibular OSCs. Next, a survey was designed to gather clinicodemographic information, OSC characteristics, participation measures, perceived outcomes, and influence on medical decision-making. The anonymous instrument was posted to two OSCs that provide support for patients with general vestibular symptoms.

Results

Seventy-three OSCs were identified with >250,000 cumulative members and >10,000 posts per month. The survey was completed by 549 participants, a cohort of primarily educated middle-aged (median = 50, interquartile range 40–60), non-Hispanic white (84%), and female (89%) participants. The participants' most cited initial motivation and achieved goal of participants was to hear from others with the same diagnosis (89% and 88%, respectively). Daily users and those who reported seeing ≥5 providers before receiving a diagnosis indicated that OSC utilization significantly influenced their requested medical treatments (72% daily vs. 61% nondaily, P = .012; 61% <5 providers vs. 71% ≥5 providers P = .019, respectively). Most participants agreed that OSC engagement provides emotional support (74%) and helps to develop coping strategies (68%). Membership of ≥1 year was associated with a higher rate of learned coping skills (61% membership <1-year vs. 71% ≥1-year P = .016).

Conclusions

The use of OSCs is widespread among vestibular diagnoses. A survey of two OSCs suggests these groups provide a significant source of peer support and can influence users' ability to interface with the medical system.

Level of Evidence

NA Laryngoscope, 132:1835–1842, 2022

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