Table 1.
Description of study population (N=316).a
Characteristics | n (%) | ||
Out-of-home caregivers |
|
||
|
Age |
|
|
|
|
18-29 | 38 (12.0) |
|
|
30-44 | 86 (27.2) |
|
|
45-59 | 101 (32.0) |
|
|
≥60 | 91 (28.8) |
|
Female | 199 (63.0) | |
|
Education |
|
|
|
|
Less than high school | 29 (9.2) |
|
|
High school degree | 72 (22.8) |
|
|
Some college | 112 (35.4) |
|
|
College degree or higher | 103 (32.6) |
|
Race/ethnicity |
|
|
|
|
White, Non-Hispanic | 189 (59.8) |
|
|
Black, Non-Hispanic | 71 (22.5) |
|
|
Hispanic | 56 (17.7) |
|
Geographic Region |
|
|
|
|
Northwest | 57 (18.0) |
|
|
Midwest | 62 (19.6) |
|
|
South | 130 (41.1) |
|
|
West | 67 (21.2) |
|
Out-of-home caregiving activities (time frame) |
|
|
|
|
Assistance with independent activities of daily living (past 3 months) (N=314) | 138 (44.0) |
|
|
Assistance with health-related tasks (past 3 months) (N=312) | 69 (22.1) |
|
|
Frequent discussions about health with care recipient (N=316) | 131 (41.5) |
|
|
Phone conversations with care recipient’s doctor (past 12 months) (N=310) | 43 (13.9) |
|
|
Suggested questions for care recipient to ask health care provider (past 12 months) (N=308) | 262 (85.1) |
|
Independent Internet accessb | 241 (76.3) | |
|
Comfort with technology |
|
|
|
|
Very low/low | 88 (27.9) |
|
|
Moderate | 114 (36.1) |
|
|
High | 114 (36.1) |
Care recipients c |
|
||
|
Age (N=313) |
|
|
|
|
<50 | 68 (21.7) |
|
|
60-64 | 90 (28.8) |
|
|
65-74 | 83 (26.5) |
|
|
≥75 | 72 (23.0) |
|
Use Internet | 183 (57.9) | |
|
Health status |
|
|
|
|
Very good or excellent | 53 (16.8) |
|
|
Good | 121 (38.3) |
|
|
Fair or poor | 142 (44.9) |
|
Relationship with caregiver |
|
|
|
|
Spouse/partner | 4 (1.3) |
|
|
Adult child | 26 (8.2) |
|
|
Sibling | 88 (27.9) |
|
|
Parent or parent-in-law | 124 (39.2) |
|
|
Other relative/friend | 74 (23.4) |
|
Distance from caregiver (N=312) |
|
|
|
|
<5 miles | 74 (23.7) |
|
|
5-20 | 85 (27.2) |
|
|
21-100 | 44 (14.1) |
|
|
>100 | 109 (34.9) |
aN=316 unless otherwise specified.
bKnowledge Networks provides Internet access to panel participants who do not have independent access.
cAll care recipient characteristics are caregiver-reported.