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. Author manuscript; available in PMC: 2020 Oct 1.
Published in final edited form as: J Empir Res Hum Res Ethics. 2019 Jul 22;14(4):328–337. doi: 10.1177/1556264619862467

Table 1:

Demographic characteristics of study participants assigned to simulation of consent to a (hypothetical) depression or diabetes genetic protocol

Simulated Genetics Protocol Depression Diabetes P value
N=47 N=30
Gender %, (n) 0.9
   Men 45% (21) 43% (13)
   Women 55% (26) 57% (17)
Age* (yrs) 39 [32, 48] 41 [36, 51] 0.309
Education %, (n) 0.059
   Less than HS 6% (3) 9% (3)
   HS or GED 38% (18) 23% (7)
   Some college or 2-year
degree 40% (18) 38% (12)
   College 2% (1) 20% (6)
   Graduate degree 15% (7) 7% (2)
Marital Status %, (n) 0.006
   Single 47% (22) 13% (4)
   Divorced or widowed 21% (10) 23% (7)
   Married/Partner 32% (15) 63% (19)
Race %, (n) 0.006
   Hispanic 26% (11) 52% (14)
   Native American 19% (8) 30% (8)
   White 56% (24) 19% (5)
*

mean and interquartile range reported