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Results: 1 to 20 of 122

Similar articles for PubMed (Select 23324203)

1.

Improving informed consent with minority participants: results from researcher and community surveys.

Quinn SC, Garza MA, Butler J, Fryer CS, Casper ET, Thomas SB, Barnard D, Kim KH.

J Empir Res Hum Res Ethics. 2012 Dec;7(5):44-55. doi: 10.1525/jer.2012.7.5.44.

2.

Reasons for enrollment, the informed consent process, and trust among low-income women participating in a community-based participatory research study.

Kneipp SM, Lutz BJ, Means D.

Public Health Nurs. 2009 Jul-Aug;26(4):362-9. doi: 10.1111/j.1525-1446.2009.00791.x.

PMID:
19573215
3.

A qualitative study using traditional community assemblies to investigate community perspectives on informed consent and research participation in western Kenya.

Vreeman R, Kamaara E, Kamanda A, Ayuku D, Nyandiko W, Atwoli L, Ayaya S, Gisore P, Scanlon M, Braitstein P.

BMC Med Ethics. 2012 Sep 25;13:23. doi: 10.1186/1472-6939-13-23.

4.

Are racial and ethnic minorities less willing to participate in health research?

Wendler D, Kington R, Madans J, Van Wye G, Christ-Schmidt H, Pratt LA, Brawley OW, Gross CP, Emanuel E.

PLoS Med. 2006 Feb;3(2):e19. Epub 2005 Dec 6. Review.

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6.

Securing recruitment and obtaining informed consent in minority ethnic groups in the UK.

Lloyd CE, Johnson MR, Mughal S, Sturt JA, Collins GS, Roy T, Bibi R, Barnett AH.

BMC Health Serv Res. 2008 Mar 30;8:68. doi: 10.1186/1472-6963-8-68.

7.

An exploration of community leader perspectives about minority involvement in chiropractic clinical research.

Polipnick J, Hondras MA, Delevan SM, Lawrence DJ.

J Altern Complement Med. 2005 Dec;11(6):1015-20.

PMID:
16398592
8.

Race, medical researcher distrust, perceived harm, and willingness to participate in cardiovascular prevention trials.

Braunstein JB, Sherber NS, Schulman SP, Ding EL, Powe NR.

Medicine (Baltimore). 2008 Jan;87(1):1-9. doi: 10.1097/MD.0b013e3181625d78.

PMID:
18204365
9.

Cultivating a cycle of trust with diverse communities in practice-based research: a report from PRIME Net.

Getrich CM, Sussman AL, Campbell-Voytal K, Tsoh JY, Williams RL, Brown AE, Potter MB, Spears W, Weller N, Pascoe J, Schwartz K, Neale AV.

Ann Fam Med. 2013 Nov-Dec;11(6):550-8. doi: 10.1370/afm.1543.

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11.

Procedures of recruiting, obtaining informed consent, and compensating research participants in Qatar: findings from a qualitative investigation.

Killawi A, Khidir A, Elnashar M, Abdelrahim H, Hammoud M, Elliott H, Thurston M, Asad H, Al-Khal AL, Fetters MD.

BMC Med Ethics. 2014 Feb 4;15:9. doi: 10.1186/1472-6939-15-9.

12.

Attitudes, understanding, and concerns regarding medical research amongst Egyptians: a qualitative pilot study.

Khalil SS, Silverman HJ, Raafat M, El-Kamary S, El-Setouhy M.

BMC Med Ethics. 2007 Aug 29;8:9.

13.

Increasing minority research participation through community organization outreach.

Alvarez RA, Vasquez E, Mayorga CC, Feaster DJ, Mitrani VB.

West J Nurs Res. 2006 Aug;28(5):541-60; discussion 561-3. Review.

14.

African American children's perceptions of HIV-focused community-based participatory research.

Traube DE, Cederbaum JA, Kerkorian D, Bhupali C, McKay MM.

J Empir Res Hum Res Ethics. 2013 Feb;8(1):79-90. doi: 10.1525/jer.2013.8.1.79.

PMID:
23485673
15.

Views of US researchers about informed consent in international collaborative research.

Dawson L, Kass NE.

Soc Sci Med. 2005 Sep;61(6):1211-22. Epub 2005 Apr 9.

PMID:
15970232
16.

A rural community's involvement in the design and usability testing of a computer-based informed consent process for the Personalized Medicine Research Project.

Mahnke AN, Plasek JM, Hoffman DG, Partridge NS, Foth WS, Waudby CJ, Rasmussen LV, McManus VD, McCarty CA.

Am J Med Genet A. 2014 Jan;164A(1):129-40. doi: 10.1002/ajmg.a.36220. Epub 2013 Nov 22.

17.

Improving the informed consent process for research subjects with low literacy: a systematic review.

Tamariz L, Palacio A, Robert M, Marcus EN.

J Gen Intern Med. 2013 Jan;28(1):121-6. doi: 10.1007/s11606-012-2133-2. Epub 2012 Jul 11. Review.

18.

Impact of social stigma on the process of obtaining informed consent for genetic research on podoconiosis: a qualitative study.

Tekola F, Bull S, Farsides B, Newport MJ, Adeyemo A, Rotimi CN, Davey G.

BMC Med Ethics. 2009 Aug 22;10:13. doi: 10.1186/1472-6939-10-13.

19.

Attitudes and beliefs of African Americans toward participation in medical research.

Corbie-Smith G, Thomas SB, Williams MV, Moody-Ayers S.

J Gen Intern Med. 1999 Sep;14(9):537-46.

20.

Ethnic minority older adults participating in clinical research: developing trust.

Moreno-John G, Gachie A, Fleming CM, Nápoles-Springer A, Mutran E, Manson SM, Pérez-Stable EJ.

J Aging Health. 2004 Nov;16(5 Suppl):93S-123S.

PMID:
15448289
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