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. Author manuscript; available in PMC: 2011 Jun 14.
Published in final edited form as: Genet Med. 2010 Feb;12(2):116–121. doi: 10.1097/GIM.0b013e3181cd6689

Table 3.

Associations between race and participant responses to questions on trust and discrimination

General Questions on Trust/Discrimination n % African American % White p value

Lose insurance coverage by taking part in study
 Agree 153 28 19 0.014
 Do Not Agree/Don’t Know 608 72 81

Lose privacy when giving a sample for research
 Agree 179 29 22 0.067
 Do Not Agree/Don’t Know 585 71 18

Shouldn’t do research until we know how info used
 Agree 368 67 44 <0.001
 Do Not Agree/Don’t Know 391 33 56

Government can’t be trusted to regulate use of genetic info
 Agree 287 49 35 <0.001
 Do Not Agree/Don’t Know 468 51 65

Trust medical researchers
 Agree 707 87 94 0.007
 Do Not Agree/Don’t Know 56 13 6

Research participants may be deceived by researchers
 Agree 226 44 27 <0.001
 Do Not Agree/Don’t Know 533 56 73

Researchers want to know more than they need to know
 Agree 145 36 15 <0.001
 Do Not Agree/Don’t Know 619 64 18

Researchers do harmful experiments w/o pt’s knowledge
 Agree 194 40 22 <0.001
 Do Not Agree/Don’t Know 569 60 78

Medical researchers use minorities as guinea pigs
 Agree 77 27 6 <0.001
 Do Not Agree/Don’t Know 684 73 94