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. Author manuscript; available in PMC: 2024 Aug 1.
Published in final edited form as: Palliat Support Care. 2024 Feb;22(1):10–18. doi: 10.1017/S1478951523000901

Table 2.

Patient and caregiver demographic characteristics

Characteristic Patient N (%) Caregiver N (%)
Age (continuous) [M(SD)] 59.6 (8.7) 55.3 (14.0)
Gender identity
  Male 10 (45.5%) 11 (50.0%)
  Female 12 (54.5%) 11 (50.0%)
Race
  White/Caucasian 4 (18.2%) 6 (27.3%)
  Black/African American 13 (59.1%) 12 (54.5%)
  Asian -- 1 (4.5%)
  Other (Hispanic or Latino/Latina) 5 (22.7%) 2 (9.1%)
Ethnicity
  Hispanic or Latino/Latina 6 (27.3%) 4 (18.2%)
  Not Hispanic or Latino/Latina 16 (72.7%) 18 (81.8%)
Employed
  Yes 6 (27.3%) 12 (54.5%)
  No 16 (72.7%) 10 (45.5%)
Married or partnered
  Yes 12 (54.6%) 13 (59.1%)
  No 10 (45.4%) 11 (40.9%)
Have children
  Yes 17 (77.3%) 14 (63.6%)
  No 5 (22.7%) 8 (36.4%)
College degree or higher
  Yes 12 (54.5%) 11 (50.0%)
  No 10 (45.5%) 11 (50.0%)
Income (<$21,000)
  Yes 5 (22.7%) 4 (18.2%)
  No 14 (63.6%) 11 (49.9%)
  Don’t know 1 (4.5%) 3 (13.6%)
  Refuse to answer 2 (9.1%) 4 (18.2%)
Health insurance coverage
  Yes 22 (100.0%) --
  No 0 (0.0%) --
Informal caregiver type
  Spouse or partner 11 (50.0%) 9 (40.9%)
  Sibling 3 (13.6%) 2 (9.1%)
  Parent 3 (13.6%) 0 (0.0%)
  Son or daughter 2 (9.1%) 5 (22.7%)
  Friend 3 (13.6%) 4 (18.2%)
  Other 0 (0.0%) 1 (4.5%)