How did we do our research?
To do our research, we wanted to work with:
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We did this by: | |
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We explain each of these on the following pages.
Our co-design group
Co-design is when people work together to plan something new. | |
When our research project started, we made a co‑design group. | |
The co-design group included people with different disabilities. | |
At the start of our research project, the co‑design group gave us ideas about how to connect with people with disability. |
And at the end of our research project, the co-design group had a meeting about:
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We used the ideas from their meeting to write this report. |
Research participants
A research participant is someone who takes part in a research project. We also call them participants. | |
We had 36 participants in our research. | |
Most of the participants lived in Adelaide. | |
And the participants had lots of different disabilities. | |
We had participants with a physical disability. A physical disability affects how someone moves and uses their body. | |
We also had participants with a cognitive disability. A cognitive disability affects how someone:
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And we had participants with an intellectual disability. An intellectual disability affects how someone can:
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We had participants with a disability that affects how they see or hear. | |
We also had participants with a brain injury. A brain injury can happen when someone:
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We had participants with autism. Autism is a disability that might affect how you:
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And we had participants with a psychosocial disability. A psychosocial disability comes from a person’s mental health. | |
10 of these participants were culturally and linguistically diverse (CaLD) people. |
CaLD people: | |
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But we didn’t have any Aboriginal or Torres Strait Islander participants. |
Our focus groups
We ran 7 focus groups in October 2021. | ||
5 of these focus groups were on a video call. | ||
And 2 of these focus groups were in Adelaide. | ||
The co-design group told us we should run focus groups for different groups of people. | ||
This helps us understand what opinions these groups of people have. | ||
We also had focus groups that everyone could take part in. This meant lots of people with different experiences. |
Doing our research the right way
Before participants took part in a focus group, we asked them to give their consent. When you give your consent, you say it’s okay to do something. | |
And we gave the participants information that:
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This information was about: | |
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We recorded the focus groups that were online. All participants gave their consent for us to record the session. | |
All the data we collect is saved on a computer. It is protected by a password. |
The data doesn’t say who the participants are. | |
And only we can use the data. |
What affected the research?
There were some things that affected our research. It’s important we explain what these things are. | |
Most participants were from South Australia. This means we don’t know what people with disability in other parts of Australia think about the NDDA. |
The people in the CaLD focus group were from the Bhutanese community. This means we only know what the Bhutanese community thinks about the NDDA. | |
It’s important we connect with more CaLD communities to know what they think about the NDDA. | |
We didn’t have many participants with: | |
| |
|
And we didn’t have anyone in the focus groups tell us they were Aboriginal or Torres Strait Islander. | |
It’s important we try to connect with these groups to find out what they think. |
How did we do our research?
To do our research, we wanted to work with:
| |
We did this by: | |
| |
| |
|
We explain each of these on the following pages.
Our co-design group
Co-design is when people work together to plan something new. | |
When our research project started, we made a co‑design group. | |
The co-design group included people with different disabilities. | |
At the start of our research project, the co‑design group gave us ideas about how to connect with people with disability. |
And at the end of our research project, the co-design group had a meeting about:
| |
We used the ideas from their meeting to write this report. |
Research participants
A research participant is someone who takes part in a research project. We also call them participants. | |
We had 36 participants in our research. | |
Most of the participants lived in Adelaide. | |
And the participants had lots of different disabilities. | |
We had participants with a physical disability. A physical disability affects how someone moves and uses their body. | |
We also had participants with a cognitive disability. A cognitive disability affects how someone:
| |
And we had participants with an intellectual disability. An intellectual disability affects how someone can:
| |
We had participants with a disability that affects how they see or hear. | |
We also had participants with a brain injury. A brain injury can happen when someone:
|
We had participants with autism. Autism is a disability that might affect how you:
| |
And we had participants with a psychosocial disability. A psychosocial disability comes from a person’s mental health. | |
10 of these participants were culturally and linguistically diverse (CaLD) people. |
CaLD people: | |
| |
| |
But we didn’t have any Aboriginal or Torres Strait Islander participants. |
Our focus groups
We ran 7 focus groups in October 2021. | ||
5 of these focus groups were on a video call. | ||
And 2 of these focus groups were in Adelaide. | ||
The co-design group told us we should run focus groups for different groups of people. | ||
This helps us understand what opinions these groups of people have. | ||
We also had focus groups that everyone could take part in. This meant lots of people with different experiences. |
Doing our research the right way
Before participants took part in a focus group, we asked them to give their consent. When you give your consent, you say it’s okay to do something. | |
And we gave the participants information that:
| |
This information was about: | |
| |
| |
We recorded the focus groups that were online. All participants gave their consent for us to record the session. | |
All the data we collect is saved on a computer. It is protected by a password. |
The data doesn’t say who the participants are. | |
And only we can use the data. |
What affected the research?
There were some things that affected our research. It’s important we explain what these things are. | |
Most participants were from South Australia. This means we don’t know what people with disability in other parts of Australia think about the NDDA. |
The people in the CaLD focus group were from the Bhutanese community. This means we only know what the Bhutanese community thinks about the NDDA. | |
It’s important we connect with more CaLD communities to know what they think about the NDDA. | |
We didn’t have many participants with: | |
| |
|
And we didn’t have anyone in the focus groups tell us they were Aboriginal or Torres Strait Islander. | |
It’s important we try to connect with these groups to find out what they think. |