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Table 2 Demographics of the Web-based survey participants

From: Impact of Alzheimer’s Disease on Caregiver Questionnaire: internal consistency, convergent validity, and test-retest reliability of a new measure for assessing caregiver burden

Type of characteristics

Baseline web-based survey (N = 200)

Re-test web-based survey (N = 50)

Age

n

%

n

%

 18–29 years

22

11.0%

6

12.0%

 30–49 years

79

39.5%

22

44.0%

 50–69 years

94

47.0%

21

42.0%

 ≥ 70 years

5

2.5%

1

2.0%

Gender

    

 Male

80

40.0%

19

38.0%

 Female

120

60.0%

31

62.0%

Race

    

 White

169

84.5%

42

84.0%

 Black/African American

14

7.0%

4

8.0%

 Asian

9

4.5%

4

8.0%

 American Indian/Alaskan Native

2

1.0%

0

0.0%

 Other

6

3.0%

0

0.0%

History being an AD caregiver

    

 < 6 months

20

10.0%

2

4.0%

 6–12 months

45

22.5%

6

12.0%

 13–24 months

51

25.5%

14

28.0%

 > 2 years

84

42.0%

28

56.0%

Employment status

    

 Full-time homemaker

16

8.0%

4

8.0%

 Employed full time (≥30 hours per week)

85

42.5%

26

52.0%

 Employed part time because of caregiving responsibilities (<30 hours per week)

26

13.0%

9

18.0%

 Employed part time not because of caregiving responsibilities (<30 hours per week)

11

5.5%

5

10.0%

 Unemployed because of caregiving responsibilities

17

8.5%

4

8.0%

 Unemployed not because of caregiving responsibilities

11

5.5%

0

0.0%

 Volunteer/Student

4

2.0%

0

0.0%

 Retired

26

13.0%

1

2.0%

 Other

4

2.0%

1

2.0%

Days per month missed from work due to caregiving duties

    

 0–5 days

82

67.2%

22

44.0%

 6–10 days

28

22.9%

16

32.0%

 11–15 days

8

6.6%

1

2.0%

 16–20 days

1

0.8%

1

2.0%

 21–24 days

3

2.5%

0

0.0%

  1. Abbreviation: AD, Alzheimer’s disease.