Literature DB >> 30899094

Disability inclusion in precision medicine research: a first national survey.

Maya Sabatello1, Ying Chen2, Yuan Zhang3, Paul S Appelbaum4.   

Abstract

PURPOSE: Including people with disabilities in precision medicine research (PMR) is key for increasing cohorts' diversity, improving understanding of population health, and attaining social justice for the United States' largest health disparities group. We conducted a national survey to explore the views of people with disabilities about PMR.
METHODS: An online survey was developed in disability-accessible formats. Key questions included views on PMR, willingness to participate and to provide data, perceived barriers to participation and potential remedies, and interest in engagement in the study. Analyses described results for all participants and compared results for key demographic characteristics.
RESULTS: In total, 1294 participants completed the survey. Participants expressed strong support for PMR, and willingness to participate in PMR; to provide lifestyle, biological, and medical information; and to engage with the study. However, 76% identified a total of 3 to 8 barriers to participation, and most would not provide environmental samples or information from their social media account(s) and activity trackers. Differences were observed across racial, ethnic, and gender groups and are discussed.
CONCLUSIONS: Barriers to disability inclusion need to be removed, and further research conducted to better understand concerns about PMR and to develop studies that resonate with the interests and needs of this population.

Entities:  

Keywords:  barriers; disability; engagement; precision medicine research

Mesh:

Year:  2019        PMID: 30899094      PMCID: PMC6755064          DOI: 10.1038/s41436-019-0486-1

Source DB:  PubMed          Journal:  Genet Med        ISSN: 1098-3600            Impact factor:   8.822


  27 in total

1.  Conducting Accessible Research: Including People With Disabilities in Public Health, Epidemiological, and Outcomes Studies.

Authors:  Dianne Rios; Susan Magasi; Catherine Novak; Mark Harniss
Journal:  Am J Public Health       Date:  2016-10-13       Impact factor: 9.308

Review 2.  Health disparities between women with and without disabilities: a review of the research.

Authors:  Jennifer P Wisdom; Marjorie G McGee; Willi Horner-Johnson; Yvonne L Michael; Elizabeth Adams; Michelle Berlin
Journal:  Soc Work Public Health       Date:  2010-05

3.  Universal design of research: inclusion of persons with disabilities in mainstream biomedical studies.

Authors:  Ann S Williams; Shirley M Moore
Journal:  Sci Transl Med       Date:  2011-05-11       Impact factor: 17.956

4.  Balancing the risks and benefits of genomic data sharing: genome research participants' perspectives.

Authors:  J M Oliver; M J Slashinski; T Wang; P A Kelly; S G Hilsenbeck; A L McGuire
Journal:  Public Health Genomics       Date:  2011-12-30       Impact factor: 2.000

5.  "If I could in a small way help": motivations for and beliefs about sample donation for genetic research.

Authors:  Marsha Michie; Gail Henderson; Joanne Garrett; Giselle Corbie-Smith
Journal:  J Empir Res Hum Res Ethics       Date:  2011-06       Impact factor: 1.742

6.  "You can't be cold and scientific": community views on ethical issues in intellectual disability research.

Authors:  Katherine E McDonald; Nicole M Schwartz; Colleen M Gibbons; Robert S Olick
Journal:  J Empir Res Hum Res Ethics       Date:  2015-03-13       Impact factor: 1.742

7.  Biobanking for research: a survey of patient population attitudes and understanding.

Authors:  Alanna Kulchak Rahm; Michelle Wrenn; Nikki M Carroll; Heather Spencer Feigelson
Journal:  J Community Genet       Date:  2013-04-20

8.  Public opinion about the importance of privacy in biobank research.

Authors:  David J Kaufman; Juli Murphy-Bollinger; Joan Scott; Kathy L Hudson
Journal:  Am J Hum Genet       Date:  2009-10-29       Impact factor: 11.025

9.  Increasing genomic literacy among adolescents.

Authors:  Maya Sabatello; Ying Chen; Saskia C Sanderson; Wendy K Chung; Paul S Appelbaum
Journal:  Genet Med       Date:  2018-09-14       Impact factor: 8.822

10.  A Survey of U.S Adults' Opinions about Conduct of a Nationwide Precision Medicine Initiative® Cohort Study of Genes and Environment.

Authors:  David J Kaufman; Rebecca Baker; Lauren C Milner; Stephanie Devaney; Kathy L Hudson
Journal:  PLoS One       Date:  2016-08-17       Impact factor: 3.240

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  11 in total

Review 1.  International Society of Psychiatric Genetics Ethics Committee: Issues facing us.

Authors:  Gabriel Lázaro-Muñoz; Maya Sabatello; Laura Huckins; Holly Peay; Franziska Degenhardt; Bettina Meiser; Todd Lencz; Takahiro Soda; Anna Docherty; David Crepaz-Keay; Jehannine Austin; Roseann E Peterson; Lea K Davis
Journal:  Am J Med Genet B Neuropsychiatr Genet       Date:  2019-05-23       Impact factor: 3.568

2.  "Just tell me what's going on": The views of parents of children with genetic conditions regarding the research use of their child's electronic health record.

Authors:  Sara M Andrews; Melissa Raspa; Anne Edwards; Rebecca Moultrie; Lauren Turner-Brown; Laura Wagner; Alexandra Alvarez Rivas; Mary Katherine Frisch; Anne C Wheeler
Journal:  J Am Med Inform Assoc       Date:  2020-03-01       Impact factor: 4.497

3.  Facilitating the inclusion of adults with intellectual disability as direct respondents in research: Strategies for fostering trust, respect, accessibility and engagement.

Authors:  Katherine E McDonald; Colleen Gibbons; Nicole Conroy; Robert S Olick
Journal:  J Appl Res Intellect Disabil       Date:  2021-09-24

Review 4.  Addressing underrepresentation in genomics research through community engagement.

Authors:  Amy A Lemke; Edward D Esplin; Aaron J Goldenberg; Claudia Gonzaga-Jauregui; Neil A Hanchard; Julie Harris-Wai; Justin E Ideozu; Rosario Isasi; Andrew P Landstrom; Anya E R Prince; Erin Turbitt; Maya Sabatello; Samantha A Schrier Vergano; Matthew R G Taylor; Joon-Ho Yu; Kyle B Brothers; Nanibaa' A Garrison
Journal:  Am J Hum Genet       Date:  2022-09-01       Impact factor: 11.043

5.  In Different Voices: The Views of People with Disabilities about Return of Results from Precision Medicine Research.

Authors:  Maya Sabatello; Yuan Zhang; Ying Chen; Paul S Appelbaum
Journal:  Public Health Genomics       Date:  2020-04-15       Impact factor: 2.000

6.  Preferences for Accessing Electronic Health Records for Research Purposes: Views of Parents Who Have a Child With a Known or Suspected Genetic Condition.

Authors:  Melissa Raspa; Ryan S Paquin; Derek S Brown; Sara Andrews; Anne Edwards; Rebecca Moultrie; Laura Wagner; MaryKate Frisch; Lauren Turner-Brown; Anne C Wheeler
Journal:  Value Health       Date:  2020-10-26       Impact factor: 5.725

Review 7.  Long overdue: including adults with brain disorders in precision health initiatives.

Authors:  Brenda M Finucane; Scott M Myers; Christa L Martin; David H Ledbetter
Journal:  Curr Opin Genet Dev       Date:  2020-06-13       Impact factor: 5.578

8.  Teenagers and Precision Psychiatry: A Window of Opportunity.

Authors:  Maya Sabatello; Ying Chen; Carmen Fiorella Herrera; Erika Brockhoff; Jehannine Austin; Paul S Appelbaum
Journal:  Public Health Genomics       Date:  2021-01-27       Impact factor: 2.000

Review 9.  Ethical, Legal, and Social Issues Related to the Inclusion of Individuals With Intellectual Disabilities in Electronic Health Record Research: Scoping Review.

Authors:  Melissa Raspa; Rebecca Moultrie; Laura Wagner; Anne Edwards; Sara Andrews; Mary Katherine Frisch; Lauren Turner-Brown; Anne Wheeler
Journal:  J Med Internet Res       Date:  2020-05-21       Impact factor: 5.428

10.  A survey study of the attitudes and experiences of adults with intellectual disability regarding participation in research.

Authors:  N E Conroy; K E McDonald; R S Olick
Journal:  J Intellect Disabil Res       Date:  2021-08-09
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