The Support, Educate, Empower personalized glaucoma coaching trial design

Author:

Newman-Casey Paula Anne12ORCID,Resnicow Ken23,Winter Suzanne1,Niziol Leslie M1,Darnley-Fisch Deborah4,Imami Nauman4,McHaney-Conner Phalatha1,Musch David C125ORCID,Mitchell Jamie6,Heisler Michele237

Affiliation:

1. Department of Ophthalmology and Visual Sciences, University of Michigan, Ann Arbor, MI, USA

2. Institute for Healthcare Policy and Innovation, University of Michigan, Ann Arbor, MI, USA

3. Department of Health Behavior and Health Education, University of Michigan School of Public Health, Ann Arbor, MI, USA

4. Department of Ophthalmology, Henry Ford Health System, Detroit, MI, USA

5. Department of Epidemiology, University of Michigan School of Public Health, Ann Arbor, MI, USA

6. School of Social Work, University of Michigan, Ann Arbor, MI, USA

7. Department of Internal Medicine, University of Michigan, Ann Arbor, MI, USA

Abstract

Background: Glaucoma is a chronic disease that affects 3 million Americans. Glaucoma is most often asymptomatic until very late in its course when treatment is more difficult and extensive peripheral vision loss has already occurred. Taking daily medications can mitigate this vision loss, but at least half of people with glaucoma do not take their prescribed medications regularly. The purpose of this study is to improve glaucoma medication adherence among those with medically treated glaucoma and poor self-reported adherence using the Support, Educate, Empower personalized coaching program. Methods/design: This study is a two-site randomized controlled trial enrolling 230 participants with poor self-reported glaucoma medication adherence. The trial has two arms, an intervention arm and a control arm. Participants in the intervention arm receive personalized glaucoma education and motivational interviewing-based coaching over 6 months from a trained non-physician interventionist for three in-person sessions with between visit phone calls for check-ins where current adherence level is reported to participants. Participants also can elect to have visual, audio, text or automated phone call medication dose reminders. Participants in the control arm continue usual care with their physician and receive non-personalized glaucoma educational materials via mail in parallel to the three in-person coaching sessions to control for glaucoma knowledge content. All participants receive a medication adherence monitor. The primary outcome is the proportion of prescribed doses taken on schedule during the 6-month period. The secondary outcome is glaucoma related distress. The exploratory outcome is intraocular pressure. Discussion: The personalized education and motivational-interviewing-based intervention that we are testing is comprehensive in that it addresses the wide range of barriers to adherence that people with glaucoma encounter. Leveraging a custom-built web-based application to generate the personalized content and the motivational-interviewing-based prompts to guide the coaching sessions will make this program both replicable and scalable and can be integrated into clinical care utilizing trained non-physician providers. Although this type of self-management support is not currently reimbursed for glaucoma as it is for diabetes, this trial could help shape future policy change should the intervention be found effective.

Funder

National Eye Institute

Publisher

SAGE Publications

Subject

Pharmacology,General Medicine

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