| dc.creator |
Goold, Susan Dorr |
|
| dc.creator |
Myers, C. Daniel |
|
| dc.creator |
Szymecko, Lisa |
|
| dc.creator |
Cunningham Collins, Carla |
|
| dc.creator |
Martinez, Sal |
|
| dc.creator |
Ledón, Charo |
|
| dc.creator |
Campbell, Terrance R. |
|
| dc.creator |
Danis, Marion |
|
| dc.creator |
Cargill, Stephanie Solomon |
|
| dc.creator |
Kim, Hyungjin Myra |
|
| dc.creator |
Rowe, Zachary |
|
| dc.date |
2017-04-14T15:12:16Z |
|
| dc.date |
2018-05-15T21:02:51Z |
|
| dc.date |
2017-04 |
|
| dc.date.accessioned |
2022-05-19T11:50:00Z |
|
| dc.date.available |
2022-05-19T11:50:00Z |
|
| dc.identifier |
Goold, Susan Dorr; Myers, C. Daniel; Szymecko, Lisa; Cunningham Collins, Carla; Martinez, Sal; Ledón, Charo ; Campbell, Terrance R.; Danis, Marion; Cargill, Stephanie Solomon; Kim, Hyungjin Myra; Rowe, Zachary (2017). "Priorities for Patient‐Centered Outcomes Research: The Views of Minority and Underserved Communities." Health Services Research 52(2): 599-615. |
|
| dc.identifier |
0017-9124 |
|
| dc.identifier |
1475-6773 |
|
| dc.identifier |
http://hdl.handle.net/2027.42/136533 |
|
| dc.identifier |
10.1111/1475-6773.12505 |
|
| dc.identifier |
Health Services Research |
|
| dc.identifier |
Danis, M., M.M. Ginsburg, and S. Goold. 2010. “ Experience in the United States with Public Deliberation about Health Insurance Benefits Using the Small Group Decision Exercise, CHAT.” The Journal of Ambulatory Care Management 33 ( 3 ): 205. |
|
| dc.identifier |
Burkhalter, S., J. Gastil, and T. Kelshaw. 2002. “ A Conceptual Definition and Theoretical Model of Public Deliberation in Small Face to Face Groups.” Communication Theory 12: 398 – 422. |
|
| dc.identifier |
National Science Foundation. 2010. “ Open Government Initiative 2010 ” [accessed on December 2, 2010]. Available at http://www.nsf.gov/open/ |
|
| dc.identifier |
Goold, S.D., A.K. Biddle, G. Klipp, C.N. Hall, and M. Danis. 2005. “ Choosing Healthplans All Together: A Deliberative Exercise for Allocating Limited Health Care Resources.” Journal of Health Politics, Policy and Law 30 ( 4 ): 563 – 602. |
|
| dc.identifier |
Goold, S.D. 1996. “ Allocating Health Care Resources: Cost Utility Analysis, Informed Democratic Decision Making, or the Veil of Ignorance? ” Journal of Health Politics, Policy and Law 21 ( 1 ): 69 – 98. |
|
| dc.identifier |
Fleck, L.M.. 2001 “ Healthcare Justice and Rational Democratic Deliberation.” American Journal of Bioethics 1 ( 2 ): 20 – 1. |
|
| dc.identifier |
Fleck, L.M. 1992. “ Just Health Care Rationing: A Democratic Decision Making Approach.” University of Pennsylvania Law Review 140 ( 5 ): 1597 – 636. |
|
| dc.identifier |
Fishkin, J.F. 1997. The Voice of the People. New Haven, CT: Yale University Press. |
|
| dc.identifier |
Cohen, J. 1997. “ Deliberation and Democratic Legitimacy.” In Deliberative Democracy: Essays on Reasons and Politics, edited by J.F. Bohman, and W. Rehg, pp. 321 – 48. Cambridge, MA: The Massachusetts Institute of Technology Press. |
|
| dc.identifier |
Vayena, E. 2014. “ The Next Step in the Patient Revolution: Patients Initiating and Leading Research.” British Medical Journal 349: g4318. |
|
| dc.identifier |
Tallon, D., J. Chard, and P. Dieppe. 2000. “ Relation between Agendas of the Research Community and the Research Consumer.” The Lancet 355 ( 9220 ): 2037 – 40. |
|
| dc.identifier |
StataCorp. 2013. Stata Statistical Software: Release 13. College Station, TX: StataCorp LP. |
|
| dc.identifier |
Solomon, S., and J. Abelson. 2012. “ Why and When Should We Use Public Deliberation? ” Hastings Center Report 42 ( 2 ): 17 – 20. |
|
| dc.identifier |
Rowe, G., D. Rawsthorne, T. Scarpello, and J.R. Dainty. 2010. “ Public Engagement in Research Funding: A Study of Public Capacities and Engagement Methodology.” Public Understanding of Science 19 ( 2 ): 225 – 39, 1: 1‐15. |
|
| dc.identifier |
PPACA Sec. 6301 D Sec 1181 (d) (1) |
|
| dc.identifier |
Patient Protection and Affordable Care Act. 2010. |
|
| dc.identifier.uri |
http://localhost:8080/xmlui/handle/CUHPOERS/107012 |
|
| dc.description |
Peer Reviewed |
|
| dc.description |
https://deepblue.lib.umich.edu/bitstream/2027.42/136533/1/hesr12505_am.pdf |
|
| dc.description |
https://deepblue.lib.umich.edu/bitstream/2027.42/136533/2/hesr12505.pdf |
|
| dc.description |
https://deepblue.lib.umich.edu/bitstream/2027.42/136533/3/hesr12505-sup-0001-AppendixSA1.pdf |
|
| dc.description |
https://deepblue.lib.umich.edu/bitstream/2027.42/136533/4/hesr12505-sup-0002-AppendixSA2.pdf |
|
| dc.format |
application/pdf |
|
| dc.format |
application/pdf |
|
| dc.format |
application/pdf |
|
| dc.format |
application/pdf |
|
| dc.publisher |
Wiley Periodicals, Inc. |
|
| dc.publisher |
The Massachusetts Institute of Technology Press |
|
| dc.rights |
IndexNoFollow |
|
| dc.subject |
decision making |
|
| dc.subject |
minority groups |
|
| dc.subject |
Patient‐centered outcomes research |
|
| dc.subject |
resource allocation |
|
| dc.subject |
research priorities |
|
| dc.subject |
Public Health |
|
| dc.subject |
Health Sciences |
|
| dc.title |
Priorities for Patient‐Centered Outcomes Research: The Views of Minority and Underserved Communities |
|
| dc.type |
Article |
|