There is currently a significant unmet need for effective and efficiently delivered care for people living with Parkinson’s. Through this new care pathway, we have shown the benefits of empowering people with knowledge and understanding of their condition. These benefits are felt not only by the people with Parkinson’s and their partners, but also the healthcare teams and organisations providing their care. With support from NHSE Transformation, we are now creating a digital version of this care pathway, which we hope will eventually enable it to be made available through Parkinson’s services across the UK.
Professor Camille Carroll
Professor of Clinical Neuroscience
People with Parkinson’s know the current model – where you travel to a hospital to see a neurologist once a year, if you’re lucky – is not working for them or their doctors. How much better to have a flexible home-based system where you’re able to contact a variety of healthcare professionals as and when the need arises, backed up by new technology to give a far more granular readout of your symptoms than that provided by that annual walk around the doctor’s office. It’s fantastic to see such an approach working for people with Parkinson’s in the South West – the challenge we now need to overcome is how to ensure everyone with the condition, wherever they are living, can benefit in a similar fashion.
Podcaster and technology writer, who chairing an Advisory Group looking at ways to roll out the Home Based Care pathway more widely
Parkinson’s UK provides grants to projects that aim to improve Parkinson's health and care services across the UK through the Parkinson’s Excellence Network. We were pleased to award a grant to this project in 2018. The study clearly shows that the remotely-delivered Parkinson's care pathway is a safe and feasible model and we are excited by the potential benefits for people with Parkinson's, particularly those from underserved communities. We look forward to seeing the work progress including the results of formal comparisons with standard care.
Associate Director of Policy & Health Strategy at Parkinson’s UK
- The full study – Kehagia, Carroll et al: Real-World Evaluation of the Feasibility, Acceptability and Safety of a Remote, Self-Management Parkinson’s Disease Care Pathway: A Healthcare Improvement Initiative – is published in the Journal of Parkinson’s Disease, DOI: 10.3233/JPD-230205.
A patient perspective on the Home Based Care pathway
“I always remember one of my first consultants telling me that I, and my wife, would possibly be the two key people when it comes to managing my Parkinson’s. So we have always been closely aware of any changes in how I am feeling or behaving, and the HBC programme encourages that as well. It does help you feel more confident and empowered, and I know that if I have any issues the doctors and nurses are just a phone call away.”
“Through these groups, people often say to me that they wish the Home Based Care pathway was offered across the UK. Making more people aware of it, and ensuring they understand what can be gained from it, is always going to be a challenge but hopefully these results will help that.”
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