Skip to main content

Table 4 Investigated influences

From: Influences on the access to and use of formal community care by people with dementia and their informal caregivers: a scoping review

Main topic n = 94

Quantitative studies

Qualitative studies

Mixed method

Attitudes towards services

n = 18

[17, 51, 71, 73, 74, 78, 87, 91]

n = 8

[103, 106, 107, 111, 117,118,119, 128, 129]

n = 9

[131]

n = 1

Ethnicity

n = 14

[28, 46, 52, 64, 88, 94]

n = 6

[97, 108, 113, 121, 123, 125, 126, 130]

n = 8

 

Various influences

n = 12

[48,49,50, 59,60,61, 65, 77, 82, 86, 92]

n = 11

 

[134]

n = 1

Influences according to the BM/adapted BM

n = 10

[23, 27, 58, 63, 66, 67, 69, 74, 83, 89]

n = 10

  

Region of residence

n = 7

[54, 55, 64, 80]

n = 4

[99, 115, 116]

n = 3

 

Gender

n = 7

[56, 79]

n = 2

[100,101,102, 105, 124]

n = 5

 

Experiences with services

n = 5

 

[82, 109, 110, 120, 122]

n = 5

[132]

n = 1

Early-onset dementia

n = 5

[47, 57, 68]

n = 3

[98, 126]

n = 2

 

Recommendations of healthcare professionals

n = 4

[93, 95, 96]

n = 3

 

[133]

n = 1

Living alone

n = 4

[52, 53, 84, 90]

n = 4

  

Barriers to service use

n = 3

[62]

n = 1

[104, 127]

n = 2

 

Needs of people with dementia or informal carers

n = 3

[70, 81, 85]

n = 3

  

Financial factors

n = 2

[75, 76]

n = 2

  

Religiousness

n = 2

[79]

n = 1

[113]

n = 1

 

Psychosocial factors

n = 1

[72]

n = 1