Literature DB >> 25954442

Sharing my health data: a survey of data sharing preferences of healthy individuals.

Elizabeth A Bell1, Lucila Ohno-Machado2, M Adela Grando3.   

Abstract

We interviewed 70 healthy volunteers to understand their choices about how the information in their health record should be shared for research. Twenty-eight survey questions captured individual preferences of healthy volunteers. The results showed that respondents felt comfortable participating in research if they were given choices about which portions of their medical data would be shared, and with whom those data would be shared. Respondents indicated a strong preference towards controlling access to specific data (83%), and a large proportion (68%) indicated concern about the possibility of their data being used by for-profit entities. The results suggest that transparency in the process of sharing is an important factor in the decision to share clinical data for research.

Mesh:

Year:  2014        PMID: 25954442      PMCID: PMC4419941     

Source DB:  PubMed          Journal:  AMIA Annu Symp Proc        ISSN: 1559-4076


  15 in total

1.  Ethical questions must be considered for electronic health records.

Authors:  Merle Spriggs; Michael V Arnold; Christopher M Pearce; Craig Fry
Journal:  J Med Ethics       Date:  2012-05-09       Impact factor: 2.903

2.  Nuffield Council opens consultation on use of personal biological and health data.

Authors:  Matthew Limb
Journal:  BMJ       Date:  2013-10-18

3.  Patient confidentiality in a time of care.data.

Authors:  Julian Sheather; Sophie Brannan
Journal:  BMJ       Date:  2013-11-27

4.  Consumer experience with and attitudes toward health information technology: a nationwide survey.

Authors:  Jessica S Ancker; Michael Silver; Melissa C Miller; Rainu Kaushal
Journal:  J Am Med Inform Assoc       Date:  2012-07-30       Impact factor: 4.497

Review 5.  From patients to partners: participant-centric initiatives in biomedical research.

Authors:  Jane Kaye; Liam Curren; Nick Anderson; Kelly Edwards; Stephanie M Fullerton; Nadja Kanellopoulou; David Lund; Daniel G MacArthur; Deborah Mascalzoni; James Shepherd; Patrick L Taylor; Sharon F Terry; Stefan F Winter
Journal:  Nat Rev Genet       Date:  2012-04-03       Impact factor: 53.242

6.  National survey of British public's views on use of identifiable medical data by the National Cancer Registry.

Authors:  Geraldine Barrett; Jackie A Cassell; Janet L Peacock; Michel P Coleman
Journal:  BMJ       Date:  2006-04-28

7.  Patient informed governance of distributed research networks: results and discussion from six patient focus groups.

Authors:  Laura A Mamo; Dennis K Browe; Holly C Logan; Katherine K Kim
Journal:  AMIA Annu Symp Proc       Date:  2013-11-16

8.  Giving patients granular control of personal health information: using an ethics 'Points to Consider' to inform informatics system designers.

Authors:  Eric M Meslin; Sheri A Alpert; Aaron E Carroll; Jere D Odell; William M Tierney; Peter H Schwartz
Journal:  Int J Med Inform       Date:  2013-09-04       Impact factor: 4.046

9.  A dynamic model of patient consent to sharing of medical record data.

Authors:  William G Dixon; Karen Spencer; Hawys Williams; Caroline Sanders; David Lund; Edgar A Whitley; Jane Kaye
Journal:  BMJ       Date:  2014-02-05

10.  Alternatives to project-specific consent for access to personal information for health research: insights from a public dialogue.

Authors:  Donald J Willison; Marilyn Swinton; Lisa Schwartz; Julia Abelson; Cathy Charles; David Northrup; Ji Cheng; Lehana Thabane
Journal:  BMC Med Ethics       Date:  2008-11-19       Impact factor: 2.652

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  20 in total

1.  Patient Preferences Regarding Informed Consent Models for Participation in a Learning Health Care System for Oncology.

Authors:  Rochelle D Jones; Chris Krenz; Michele Gornick; Kent A Griffith; Rebecca Spence; Angela R Bradbury; Raymond De Vries; Sarah T Hawley; Rodney A Hayward; Robin Zon; Sage Bolte; Navid Sadeghi; Richard L Schilsky; Reshma Jagsi
Journal:  JCO Oncol Pract       Date:  2020-04-30

2.  Use of the National Heart, Lung, and Blood Institute Data Repository.

Authors:  Sean A Coady; George A Mensah; Elizabeth L Wagner; Miriam E Goldfarb; Denise M Hitchcock; Carol A Giffen
Journal:  N Engl J Med       Date:  2017-03-29       Impact factor: 91.245

3.  Children's rare disease cohorts: an integrative research and clinical genomics initiative.

Authors:  Shira Rockowitz; Nicholas LeCompte; Mary Carmack; Andrew Quitadamo; Lily Wang; Meredith Park; Devon Knight; Emma Sexton; Lacey Smith; Beth Sheidley; Michael Field; Ingrid A Holm; Catherine A Brownstein; Pankaj B Agrawal; Susan Kornetsky; Annapurna Poduri; Scott B Snapper; Alan H Beggs; Timothy W Yu; David A Williams; Piotr Sliz
Journal:  NPJ Genom Med       Date:  2020-07-06       Impact factor: 8.617

4.  Perspectives of Patients With Cancer on the Ethics of Rapid-Learning Health Systems.

Authors:  Reshma Jagsi; Kent A Griffith; Aaron Sabolch; Rochelle Jones; Rebecca Spence; Raymond De Vries; David Grande; Angela R Bradbury
Journal:  J Clin Oncol       Date:  2017-05-24       Impact factor: 44.544

5.  Effect of Public Deliberation on Patient Attitudes Regarding Consent and Data Use in a Learning Health Care System for Oncology.

Authors:  Reshma Jagsi; Kent A Griffith; Rochelle D Jones; Chris Krenz; Michele Gornick; Rebecca Spence; Raymond De Vries; Sarah T Hawley; Robin Zon; Sage Bolte; Navid Sadeghi; Richard L Schilsky; Angela R Bradbury
Journal:  J Clin Oncol       Date:  2019-10-02       Impact factor: 44.544

6.  State of the art and a mixed-method personalized approach to assess patient perceptions on medical record sharing and sensitivity.

Authors:  Hiral Soni; Adela Grando; Anita Murcko; Sabrina Diaz; Madhumita Mukundan; Nassim Idouraine; George Karway; Michael Todd; Darwyn Chern; Christy Dye; Mary Jo Whitfield
Journal:  J Biomed Inform       Date:  2019-11-11       Impact factor: 6.317

7.  Research Use of Electronic Health Records: Patients' Views on Alternative Approaches to Permission.

Authors:  Catherine M Hammack-Aviran; Kathleen M Brelsford; Kevin C McKenna; Ross D Graham; Zachary M Lampron; Laura M Beskow
Journal:  AJOB Empir Bioeth       Date:  2020-04-27

8.  Sharing data for future research-engaging participants' views about data governance beyond the original project: a DIRECT Study.

Authors:  Nisha Shah; Victoria Coathup; Harriet Teare; Ian Forgie; Giuseppe Nicola Giordano; Tue Haldor Hansen; Lenka Groeneveld; Michelle Hudson; Ewan Pearson; Hartmut Ruetten; Jane Kaye
Journal:  Genet Med       Date:  2018-09-28       Impact factor: 8.822

9.  Stakeholders' views on data sharing in multicenter studies.

Authors:  Kathleen M Mazor; Allison Richards; Mia Gallagher; David E Arterburn; Marsha A Raebel; W Benjamin Nowell; Jeffrey R Curtis; Andrea R Paolino; Sengwee Toh
Journal:  J Comp Eff Res       Date:  2017-08-14       Impact factor: 1.744

10.  Privacy versus Convenience: A Historical Perspective, Analysis of Risks, and an Informatics Call to Action.

Authors:  Larry Ozeran; Anthony Solomonides; Richard Schreiber
Journal:  Appl Clin Inform       Date:  2021-05-05       Impact factor: 2.342

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