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. Author manuscript; available in PMC: 2022 May 1.
Published in final edited form as: Palliat Med. 2021 Mar 29;35(5):952–961. doi: 10.1177/02692163211004216

Table 4.

Participant characteristics

Intervention Control
Patients N=101 Caregivers N=101 Patients N=101 Caregivers N=101
Age, M(SD) 62.84 (10.34) 57.11 (12.83) 62.18 (12.44) 58.19 (12.61)
Gender, n (%)
 Female 42 (41.6%) 73 (72.3%) 41 (40.6%) 69 (68.3%)
 Male 59 (58.4%) 28 (27.7%) 60 (59.4%) 32 (31.7%)
Race, n (%)
 Black of African American 15 (16.0%) 17 (18.9%) 16 (16.5%) 16 (17.0%)
 White 78 (83.0%) 72 (80.0%) 81 (83.5%) 77 (81.9%)
 Other/unknown 1 (1.1%) 1 (1.1%) 0 (0.0%) 1 (1.1%)
Ethnicity, n (%)
 Hispanic or Latino 2 (2.0%) 4 (2.0%) 1 (1.0%) 4 (2.0%)
 Not Hispanic or Latino 99 (98.0%) 198 (98.0%) 100 (99.0%) 198 (98.0%)
Relationship to patient, n (%)
 Spouse/partner 69 (68.3%) 77 (76.2%)
 Adult child 16 (15.8%) 8 (7.9%)
 Sibling 6 (5.9%) 6 (5.9%)
 Other/unknown 10 (9.9%) 10 (9.9%)
Cancer type, n (%)
 Blood 1 (1.0%) 3 (3.0%)
 Bone 5 (5.0%) 2 (2.0%)
 Breast 7 (6.9%) 5 (5.0%)
 Gastrointestinal 32 (31.7%) 27 (26.7%)
 Lung 15 (14.8%) 24 (23.8%)
 Prostate 19 (18.8%) 13 (12.9%)
 Other/multiple 22 (21.8%) 27 (26.7%)