Resources
For patients
You can provide these resources to patients to help them before, during and post screening. See the full resource library.
Before screening appointment
- Video yarning about Aboriginal Women’s Health Business
- Fact sheet explaining self-collection and the Cervical Screening Test
During screening appointment
- Instructional video on how to take a Cervical Screening Test sample
- Visual guide on how to collect your own vaginal sample for a Cervical Screening Test
Post screening appointment
For health care providers
You can use these resources to prepare for an appointment with an Aboriginal and Torres Strait Islander woman:
- Collecting self-identified status data from Aboriginal and Torres Strait Islander patients and patients from culturally and linguistically diverse (CALD) backgrounds (PDF, 70 KB)
- An introduction to Aboriginal and Torres Strait Islander health cultural protocols and perspectives (PDF, 3.8 MB) – The Royal Australian College of General Practitioners Limited.
Considerations
Compared to non-Indigenous people, Aboriginal and Torres Strait Islander women are more likely to:
- develop invasive cervical cancer
- die from cervical cancer.
We have limited data on Indigenous women’s participation in screening. Studies suggest participation in cervical screening is 18% lower for Indigenous women than for non-Indigenous women.
It’s likely that the higher incidence and mortality from cervical cancer among Aboriginal and or Torres Strait Islander women is linked to:
- under-screening
- late detection of pre-cancerous lesions.
Barriers
There are general barriers that people face in participating in cervical screening. Aboriginal and Torres Strait Islander women face extra barriers relating to:
- shame, fear and embarrassment about cervical screening and cancer
- distrust of healthcare providers, mainstream providers and government services.
- lack of culturally sensitive and appropriate health services.
- lack of Indigenous and female healthcare providers.
- negative cultural perceptions about cancer – for example fatalistic and superstitious attitudes
- perceptions of cervical screening as unnecessary
- lack of access to health services due to distance, remoteness and transport.
- limited knowledge or awareness of the importance and benefits of cancer screening.
- prioritisation of family needs before their own health
- lack of Indigenous-specific, culturally relevant educational resources (e.g speaking posters, as very few local Central Australian languages are written or read)
- history of sexual assault
- language and literacy barriers.
Ways to engage
The strategies below are effective in engaging Aboriginal and Torres Strait Islander women in cervical screening.
| Strategy | Details |
|---|---|
| Cultural safety training | Cultural safety training for healthcare providers and practice staff will help to build an understanding of culturally-based attitudes towards:
|
| Culturally safe environment |
|
| Service flexibility |
|
| Choice of provider |
|
| Choice of screening method |
|
| Appropriate communication |
|