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. 2020 Nov 11;23(12):1631–1638. doi: 10.1089/jpm.2020.0103

Table 1.

Patient and Caregiver Characteristics

  Patients (N = 11) Caregivers (N = 11)
Age, mean (SD) 84.7 (5.7) 57.2 (13.8)
Gender, n (%)
 Male 2 (18.2) 5 (45.5)
 Female 9 (81.8) 6 (54.5)
Race/ethnicity, n (%)
 White 8 (72.7) 8 (72.7)
 Black/African American 2 (18.2) 0 (0)
 Asian/Pacific Islander 1 (9.1) 2 (18.2)
 Other 0 (0) 1 (9.1)
Education, n (%)
 ≤ High school 2 (18.2) 2 (18.2)
 Some college or technical 4 (36.4) 3 (27.3)
 College graduate 1 (9.1) 3 (27.3)
 Graduate school 4 (36.4) 3 (27.3)
Limited finances, n (%)a 0 (0) 1 (9.1)
Limited health literacy, n (%)b 5 (45.5) 0 (0)
Cognitive status, n (%)c
 Normal mental function 9 (81.8)
 Mild-to-moderate impairment 2 (18.2)
Self-reported health status, n (%)
 Fair/Poor 5 (45.5)
 Good/Very good 6 (54.5)
Positive depression or anxiety screend 4 (36.4)
Live alone, n (%) 4 (36.4)
Social support, mean (SD)e 17.2 (2.8)
Self-reported quality-of-life, n (%)
 Fair/Poor 3 (27.3)
 Good/Very good/Excellent 8 (72.7)
Experience (years) working as caregiver, mean (SD) 7.8 (5.1)
a

“Limited” if reported not having enough finances to make ends meet.

b“

Limited” if answered not at all/a little/somewhat in response to confidence about filling out medical forms.

c

By convention based on adjusted Short Portable Mental Status Questionnaire scores.

d

Positive if Patient Health Questionnaire-2 or Generalized Anxiety Disorder 2-item scale score ≥3.

e

Social support was measured using a 4-item version of the Medical Outcomes Study Social Support Survey. Scores range from 4 to 20, with 20 indicating higher support.

SD, standard deviation.