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. Author manuscript; available in PMC: 2018 May 23.
Published in final edited form as: J Palliat Care. 2018 Mar 7;33(2):100–108. doi: 10.1177/0825859718758120

Table 1b.

Caregiver Descriptive Statistics: Overall and by Care Recipient Race

Race p-value

Full Sample Black Non-Black
(N=1279) (N = 112) (N = 1167)
N (%) Mean (SD) N (%) Mean (SD) N (%) Mean (SD)
Demographics
Sex (Female) 820 (64.10) 86 (76.80) 734 (62.90) .003
Education 9.65 (3.13) 9.27 (3.40) 9.70 (3.41) .168
Relationship to Care recipient
 Spouse 459 (35.90) 19 (17.00) 440 (37.70) .000
 Son/Daughter 616 (48.20) 59 (52.70) 557 (47.70)
 Brother/Sister 49 (3.80) 10 (8.90) 39 (3.40)
 Other Relationships 155 (12.10) 24 (21.40) 131 (11.20)
Social Exchange Perspective Measure
Physical Exchange Good (Yes) 882 (69.00) 79 (70.50) 803 (68.80) .706
Social Exchange Good (Yes) 1047 (81.90) 96 (85.70) 951 (81.50) .268
Psychological Exchange Good (Yes) 1127 (88.10) 102 (91.10) 1025 (87.8) .312
Caregiver burden measures
Subjective 2.09 (2.75) 2.21 (3.10) 2.08 (2.72) .612
Objective 3.42 (4.92) 4.16 (5.37) 3.35 (4.87) .096

Note. SD, standard deviation; Subjective burden scale ranges from 0 to 12; Objective burden scale ranges from 0 to 45. p-values <. 05 are bolded to denote statistical significance.