Patient-reported outcomes via electronic health record portal versus telephone: a pragmatic randomized pilot trial of anxiety or depression symptoms in epilepsy

Author:

Munger Clary Heidi M1ORCID,Snively Beverly M2,Topaloglu Umit3ORCID,Duncan Pamela1,Kimball James4,Alexander Halley1,Brenes Gretchen A5

Affiliation:

1. Department of Neurology, Wake Forest School of Medicine , Winston-Salem, North Carolina, USA

2. Department of Biostatistics and Data Science, Wake Forest School of Medicine , Winston-Salem, North Carolina, USA

3. Department of Cancer Biology, Wake Forest School of Medicine , Winston-Salem, North Carolina, USA

4. Department of Psychiatry, Wake Forest School of Medicine , Winston-Salem, North Carolina, USA

5. Department of Internal Medicine, Section of Gerontology and Geriatric Medicine, Wake Forest School of Medicine , Winston-Salem, North Carolina, USA

Abstract

Abstract Objective To close gaps between research and clinical practice, tools are needed for efficient pragmatic trial recruitment and patient-reported outcome collection. The objective was to assess feasibility and process measures for patient-reported outcome collection in a randomized trial comparing electronic health record (EHR) patient portal questionnaires to telephone interview among adults with epilepsy and anxiety or depression symptoms. Materials and Methods Recruitment for the randomized trial began at an epilepsy clinic visit, with EHR-embedded validated anxiety and depression instruments, followed by automated EHR-based research screening consent and eligibility assessment. Fully eligible individuals later completed telephone consent, enrollment, and randomization. Participants were randomized 1:1 to EHR portal versus telephone outcome assessment, and patient-reported and process outcomes were collected at 3 and 6 months, with primary outcome 6-month retention in EHR arm (feasibility target: ≥11 participants retained). Results Participants (N = 30) were 60% women, 77% White/non-Hispanic, with mean age 42.5 years. Among 15 individuals randomized to EHR portal, 10 (67%, CI 41.7%–84.8%) met the 6-month retention endpoint, versus 100% (CI 79.6%–100%) in the telephone group (P = 0.04). EHR outcome collection at 6 months required 11.8 min less research staff time per participant than telephone (5.9, CI 3.3–7.7 vs 17.7, CI 14.1–20.2). Subsequent telephone contact after unsuccessful EHR attempts enabled near complete data collection and still saved staff time. Discussion In this randomized study, EHR portal outcome assessment did not meet the retention feasibility target, but EHR method saved research staff time compared to telephone. Conclusion While EHR portal outcome assessment was not feasible, hybrid EHR/telephone method was feasible and saved staff time.

Funder

National Center for Advancing Translational Sciences

National Institute of Neurological Disorders and Stroke

Publisher

Oxford University Press (OUP)

Subject

Health Informatics

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