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Table 2 Prevalence of virtual care use in PLWD, Care partners and Family Physicians

From: Virtual primary care for people living with dementia in Canada: cross-sectional surveys of patients, care partners, and family physicians

Variable n (%)

PLWD

Care partner (N = 341)

All

(N = 131)

Completed by PLWDs

(N = 55)

Completed by proxies

(N = 76)

Receiving virtual care

   

Yes, and I’m (we’re) already using it

81 (61.8)

38 (69.1)

43 (56.6)

209 (61.3)

Yes, but I’m (we’re) not interested

15 (11.5)

6 (10.9)

9 (11.8)

16 (4.7)

Yes, but I (we) don’t know how it works

8 (6.1)

3 (5.5)

5 (6.6)

10 (2.9)

No, and I (we) don’t want this service

5 (3.8)

1 (1.8)

4 (5.3)

32 (9.4)

No, but I (we) would like this service

7 (5.3)

1 (1.8)

6 (7.9)

25 (7.3)

Don’t know

15 (11.5)

6 (10.9)

9 (11.8)

49 (14.4)

Type of virtual care useda

   

Any virtual care (phone and/or video)

79 (61.2)

38 (69.1)

41 (55.4)

194 (59.5)

Only phone

61 (47.2)

29 (52.7)

32 (43.2)

161 (47.2)

Only video

2 (1.6)

1 (1.8)

1 (1.4)

5 (1.5)

Combination of phone and video

16 (12.4)

8 (14.5)

8 (10.8)

28 (8.5)

Missing/Don’t know what type of virtual care

2

-

2

15

 

Family Physicians (N = 125)

Providing virtual care

 

Providing any type of virtual care for all patients

109 (87.2)

Providing any type of virtual care for PLWD

96 (77.4)

Will keep using virtual care for PLWD after the COVID-19 pandemic

92 (74.2)

Missing

1

Type of virtual care provided for PWLD

 

Any virtual care (phone or video)

96 (77.4)

Only phone

48 (38.7)

Only video

2 (1.6)

Combination of phone and video

46 (37.1)

Missing

1

  1. PLWD: A person living with dementia, consenting to and completing the survey on own behalf
  2. Proxy: A caregiver, family member, or other decision-maker consenting to and completing the survey on behalf of the person living with dementia
  3. a Of those who said “Yes, and I am (we’re) already using it” and specified it