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Electronic Video Consent to Power Precision Health Research: A Pilot Cohort Study

BACKGROUND: Developing innovative, efficient, and institutionally scalable biospecimen consent for remnant tissue that meets the National Institutes of Health consent guidelines for genomic and molecular analysis is essential for precision medicine efforts in cancer. OBJECTIVE: This study aims to pi...

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Autores principales: Naeim, Arash, Dry, Sarah, Elashoff, David, Xie, Zhuoer, Petruse, Antonia, Magyar, Clara, Johansen, Liliana, Werre, Gabriela, Lajonchere, Clara, Wenger, Neil
Formato: Online Artículo Texto
Lenguaje:English
Publicado: JMIR Publications 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8459215/
https://www.ncbi.nlm.nih.gov/pubmed/34313247
http://dx.doi.org/10.2196/29123
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author Naeim, Arash
Dry, Sarah
Elashoff, David
Xie, Zhuoer
Petruse, Antonia
Magyar, Clara
Johansen, Liliana
Werre, Gabriela
Lajonchere, Clara
Wenger, Neil
author_facet Naeim, Arash
Dry, Sarah
Elashoff, David
Xie, Zhuoer
Petruse, Antonia
Magyar, Clara
Johansen, Liliana
Werre, Gabriela
Lajonchere, Clara
Wenger, Neil
author_sort Naeim, Arash
collection PubMed
description BACKGROUND: Developing innovative, efficient, and institutionally scalable biospecimen consent for remnant tissue that meets the National Institutes of Health consent guidelines for genomic and molecular analysis is essential for precision medicine efforts in cancer. OBJECTIVE: This study aims to pilot-test an electronic video consent that individuals could complete largely on their own. METHODS: The University of California, Los Angeles developed a video consenting approach designed to be comprehensive yet fast (around 5 minutes) for providing universal consent for remnant biospecimen collection for research. The approach was piloted in 175 patients who were coming in for routine services in laboratory medicine, radiology, oncology, and hospital admissions. The pilot yielded 164 completed postconsent surveys. The pilot assessed the usefulness, ease, and trustworthiness of the video consent. In addition, we explored drivers for opting in or opting out. RESULTS: The pilot demonstrated that the electronic video consent was well received by patients, with high scores for usefulness, ease, and trustworthiness even among patients that opted out of participation. The revised more animated video pilot test in phase 2 was better received in terms of ease of use (P=.005) and the ability to understand the information (P<.001). There were significant differences between those who opted in and opted out in their beliefs concerning the usefulness of tissue, trusting researchers, the importance of contributing to science, and privacy risk (P<.001). The results showed that “I trust researchers to use leftover biological specimens to promote the public’s health” and “Sharing a biological sample for research is safe because of the privacy protections in place” discriminated opt-in statuses were the strongest predictors (both areas under the curve were 0.88). Privacy concerns seemed universal in individuals who opted out. CONCLUSIONS: Efforts to better educate the community may be needed to help overcome some of the barriers in engaging individuals to participate in precision health initiatives.
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spelling pubmed-84592152021-10-18 Electronic Video Consent to Power Precision Health Research: A Pilot Cohort Study Naeim, Arash Dry, Sarah Elashoff, David Xie, Zhuoer Petruse, Antonia Magyar, Clara Johansen, Liliana Werre, Gabriela Lajonchere, Clara Wenger, Neil JMIR Form Res Original Paper BACKGROUND: Developing innovative, efficient, and institutionally scalable biospecimen consent for remnant tissue that meets the National Institutes of Health consent guidelines for genomic and molecular analysis is essential for precision medicine efforts in cancer. OBJECTIVE: This study aims to pilot-test an electronic video consent that individuals could complete largely on their own. METHODS: The University of California, Los Angeles developed a video consenting approach designed to be comprehensive yet fast (around 5 minutes) for providing universal consent for remnant biospecimen collection for research. The approach was piloted in 175 patients who were coming in for routine services in laboratory medicine, radiology, oncology, and hospital admissions. The pilot yielded 164 completed postconsent surveys. The pilot assessed the usefulness, ease, and trustworthiness of the video consent. In addition, we explored drivers for opting in or opting out. RESULTS: The pilot demonstrated that the electronic video consent was well received by patients, with high scores for usefulness, ease, and trustworthiness even among patients that opted out of participation. The revised more animated video pilot test in phase 2 was better received in terms of ease of use (P=.005) and the ability to understand the information (P<.001). There were significant differences between those who opted in and opted out in their beliefs concerning the usefulness of tissue, trusting researchers, the importance of contributing to science, and privacy risk (P<.001). The results showed that “I trust researchers to use leftover biological specimens to promote the public’s health” and “Sharing a biological sample for research is safe because of the privacy protections in place” discriminated opt-in statuses were the strongest predictors (both areas under the curve were 0.88). Privacy concerns seemed universal in individuals who opted out. CONCLUSIONS: Efforts to better educate the community may be needed to help overcome some of the barriers in engaging individuals to participate in precision health initiatives. JMIR Publications 2021-09-08 /pmc/articles/PMC8459215/ /pubmed/34313247 http://dx.doi.org/10.2196/29123 Text en ©Arash Naeim, Sarah Dry, David Elashoff, Zhuoer Xie, Antonia Petruse, Clara Magyar, Liliana Johansen, Gabriela Werre, Clara Lajonchere, Neil Wenger. Originally published in JMIR Formative Research (https://formative.jmir.org), 08.09.2021. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work, first published in JMIR Formative Research, is properly cited. The complete bibliographic information, a link to the original publication on https://formative.jmir.org, as well as this copyright and license information must be included.
spellingShingle Original Paper
Naeim, Arash
Dry, Sarah
Elashoff, David
Xie, Zhuoer
Petruse, Antonia
Magyar, Clara
Johansen, Liliana
Werre, Gabriela
Lajonchere, Clara
Wenger, Neil
Electronic Video Consent to Power Precision Health Research: A Pilot Cohort Study
title Electronic Video Consent to Power Precision Health Research: A Pilot Cohort Study
title_full Electronic Video Consent to Power Precision Health Research: A Pilot Cohort Study
title_fullStr Electronic Video Consent to Power Precision Health Research: A Pilot Cohort Study
title_full_unstemmed Electronic Video Consent to Power Precision Health Research: A Pilot Cohort Study
title_short Electronic Video Consent to Power Precision Health Research: A Pilot Cohort Study
title_sort electronic video consent to power precision health research: a pilot cohort study
topic Original Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8459215/
https://www.ncbi.nlm.nih.gov/pubmed/34313247
http://dx.doi.org/10.2196/29123
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