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Table 3 Barriers to cancer screening uptake as well as follow-up and treatment in Indigenous populations

From: Australia's National Bowel Cancer Screening Program: does it work for Indigenous Australians?

Socio-cultural and behavioural barriers

Structural barriers

Individual barriers

Access barriers

Poor knowledge and awareness of cancer and screening services

Poor coordination of services, from screening to follow-up and treatment

Low levels of health literacy

Lack of transportation

Language/literacy barriers

Distance barriers/rural residence

Low perceived risk

Frequent moving, changing address

Negative attitude

Child care commitments (family responsibilities)

Worry or fear of cancer

Inflexible clinic schedules

Fatalism regarding cancer

Lack of Indigenous staff

Low priority of screening

Difficulties negotiating/communicating with providers and organizations due to language/literacy or cultural differences

Perceived self efficacy

 

Lack of appropriate health information

 

Presence of co-morbidities

Lack of health promotion material in Indigenous languages

History of racism and distrust in medical institutions

 

Discomfort with mainstream services/alienating hospital environment

 

Absence of holistic, culturally appropriate cancer services

 
 

Economic

 

Cost of seeing a GP including transport

 

Unsure of potential costs of follow-up and treatment

 

Costs for travel and accommodation to hospital

 

Provider-related

 

Lack of understanding of cultural needs

 

Poor identification of Indigenous status

 

Lack of appropriate resources