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