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An Integrated, Scalable, Electronic Video Consent Process to Power Precision Health Research: Large, Population-Based, Cohort Implementation and Scalability Study.
Lajonchere, Clara; Naeim, Arash; Dry, Sarah; Wenger, Neil; Elashoff, David; Vangala, Sitaram; Petruse, Antonia; Ariannejad, Maryam; Magyar, Clara; Johansen, Liliana; Werre, Gabriela; Kroloff, Maxwell; Geschwind, Daniel.
  • Lajonchere C; Institute for Precision Health, David Geffen School of Medicine at UCLA, Los Angeles, CA, United States.
  • Naeim A; Center for SMART Health, Institute for Precision Health, David Geffen School of Medicine at UCLA, Los Angeles, CA, United States.
  • Dry S; Department of Pathology and Laboratory Medicine, David Geffen School of Medicine at UCLA, Los Angeles, CA, United States.
  • Wenger N; Department of Medicine, David Geffen School of Medicine at UCLA, Los Angeles, CA, United States.
  • Elashoff D; Department of Medicine, David Geffen School of Medicine at UCLA, Los Angeles, CA, United States.
  • Vangala S; Department of Medicine, David Geffen School of Medicine at UCLA, Los Angeles, CA, United States.
  • Petruse A; Embedded Clinical Research and Innovation Unit, Clinical and Translational Science Institute, David Geffen School of Medicine at UCLA, Los Angeles, CA, United States.
  • Ariannejad M; Institute for Precision Health, David Geffen School of Medicine at UCLA, Los Angeles, CA, United States.
  • Magyar C; Department of Pathology and Laboratory Medicine, David Geffen School of Medicine at UCLA, Los Angeles, CA, United States.
  • Johansen L; Embedded Clinical Research and Innovation Unit, Clinical and Translational Science Institute, David Geffen School of Medicine at UCLA, Los Angeles, CA, United States.
  • Werre G; Embedded Clinical Research and Innovation Unit, Clinical and Translational Science Institute, David Geffen School of Medicine at UCLA, Los Angeles, CA, United States.
  • Kroloff M; Department of Medicine, David Geffen School of Medicine at UCLA, Los Angeles, CA, United States.
  • Geschwind D; Institute for Precision Health, David Geffen School of Medicine at UCLA, Los Angeles, CA, United States.
J Med Internet Res ; 23(12): e31121, 2021 12 08.
Article en En | MEDLINE | ID: mdl-34889741
BACKGROUND: Obtaining explicit consent from patients to use their remnant biological samples and deidentified clinical data for research is essential for advancing precision medicine. OBJECTIVE: We aimed to describe the operational implementation and scalability of an electronic universal consent process that was used to power an institutional precision health biobank across a large academic health system. METHODS: The University of California, Los Angeles, implemented the use of innovative electronic consent videos as the primary recruitment tool for precision health research. The consent videos targeted patients aged ≥18 years across ambulatory clinical laboratories, perioperative settings, and hospital settings. Each of these major areas had slightly different workflows and patient populations. Sociodemographic information, comorbidity data, health utilization data (ambulatory visits, emergency room visits, and hospital admissions), and consent decision data were collected. RESULTS: The consenting approach proved scalable across 22 clinical sites (hospital and ambulatory settings). Over 40,000 participants completed the consent process at a rate of 800 to 1000 patients per week over a 2-year time period. Participants were representative of the adult University of California, Los Angeles, Health population. The opt-in rates in the perioperative (16,500/22,519, 73.3%) and ambulatory clinics (2308/3390, 68.1%) were higher than those in clinical laboratories (7506/14,235, 52.7%; P<.001). Patients with higher medical acuity were more likely to opt in. The multivariate analyses showed that African American (odds ratio [OR] 0.53, 95% CI 0.49-0.58; P<.001), Asian (OR 0.72, 95% CI 0.68-0.77; P<.001), and multiple-race populations (OR 0.73, 95% CI 0.69-0.77; P<.001) were less likely to participate than White individuals. CONCLUSIONS: This is one of the few large-scale, electronic video-based consent implementation programs that reports a 65.5% (26,314/40,144) average overall opt-in rate across a large academic health system. This rate is higher than those previously reported for email (3.6%) and electronic biobank (50%) informed consent rates. This study demonstrates a scalable recruitment approach for population health research.
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Medicina de Precisión / Laboratorios Clínicos Tipo de estudio: Etiology_studies / Incidence_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Límite: Adolescent / Adult / Humans Idioma: En Año: 2021 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Medicina de Precisión / Laboratorios Clínicos Tipo de estudio: Etiology_studies / Incidence_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Límite: Adolescent / Adult / Humans Idioma: En Año: 2021 Tipo del documento: Article