For many older Australians, and particularly those with dementia, relinquishing their driver’s licence is a pivotal and potentially overwhelming event.
The decision to hand over the car keys can prove difficult, leaving many feeling as if they have lost their independence. It also presents a challenge to primary carers, and GPs – often tasked with delivering the difficult news.
Dr Theresa Scott, NHMRC-ARC Research Development Fellow at the University of Queensland, is working with a research team to develop CarFreeMe – a program that will provide practical and emotional support for those advised they should stop driving.
Dr Scott has found that timing is everything when it comes to relinquishing a driver’s licence.
“The transition to non-driving comes at significant personal cost, including increased risk of depression, anxiety, loneliness and isolation, identity loss, and grief. As symptoms of dementia progress, people lose insight into their driving ability and how it may affect others. Therefore, the ideal situation is for voluntary and gradual driving cessation,” notes Dr Scott.
“Changes to driving status not only impact the individual stopping driving but also their family members supporting them. Often people are less upset with the process if they come to the conclusion themselves earlier rather than later.”
With trials currently underway, CarFreeMe is an evidence-based approach to supporting people living with dementia who are adjusting to life without driving. It is focused on the emotional and practical issues. CarFreeMe participants collaborate with a trained health professional, one-to-one and in small group sessions, to develop tailored solutions to individual needs based on their location and access to alternative forms of transport.
In addition to the trials underway in Queensland, Dr Scott’s team is developing a telehealth resource for general practitioners, primary carers and health professionals to manage this significant change.
Dr Scott hopes that this resource will be particularly helpful for general practitioners in rural and remote areas, where transport options are limited, and practitioners have often developed a relationship with patients over a significant period. In these instances, delivering the news that a patient can no longer drive can have long-term care implications, fundamentally changing the relationship and sometimes resulting in patients seeking care elsewhere.
“Clearly this is upsetting and damages the doctor-patient relationship,” says Dr Scott.
Ultimately, the CarFreeMe program and resources aim to involve families and carers in the intervention process, resulting in better outcomes for people with dementia.
“This resource will help people realise they have a life outside of driving. It was developed with input from people who have experienced driving cessation and what they said they needed to adjust and remain active and connected to their community.”
The CarFreeMe program is currently being trialled in Queensland and the ACT. If you would like further information or to participate, please visit https://www.dementia.org.au/node/82231
I commend the research program. I am a competent, considerate and careful driver. I believe my husband is not a competent driver now and so do passengers who have been with him. I have urged him to go to have his driving assessed but he laughs at the suggestion and WILL NOT allow me to drive either with him or by myself. Can you suggest a solution please. Regards Lorraine
It would have been helpful to know what “tailored solutions” have been developed. Including where the potential locations are, and what “alternative” forms of travel is to be available, and how they are to be accessed based on “individual needs?”
Nice work. We did something similar with the RMS in NSW, as one of the projects of #KiamaDFC.
I am one of the developers of the CarFreeMe program - it is available for other groups of people as well. Information about the program including the background research is at www.carfreeme.com.au and you can also contact the team about the current trials for people living with dementia. In answer to Mary's question - transport and licensing bodies within each state do not release this kind of information. We know people can feel very shocked and isolated so it is good to let people in this situation know that support is out there!
Hi Mary, you raise a really important point which is echoed in the feedback that we have received from people involved in our research. I do not know of a register of people who have just lost their licences, but please email me if you would like to discuss it further.
We have a friend with Parkinson's who is contemplating relinquishing his license. This program sounds as if it could be beneficial for more than dementia patients.
It would be so good if someone could call over and ask "how are you coping?" when one has been invalidated in yet another area of one's life. It is a most crippling experience for the driver and the carer. Do you have some kind of register of people who have just lost their licences because of Dementia?