Connecting your patients to Parkinson's research
People with Parkinson's want to hear about research. Explore practical tools to help you share opportunities with patients.
- Research
- Publications
- Tools
- Care manager
- Care worker
- Dietitian
- Doctor (geriatrician)
- Doctor (gp)
- Doctor (neurologist)
- Doctor (other)
- Healthcare assistant
- Nurse (Parkinson's nurse)
- Nurse (other)
- Occupational therapist
- Pharmacist
- Physiotherapist
- Psychiatrist
- Psychologist
- Social care assessor
- Social worker
- Speech and language therapist
- Complex
- Diagnosis
- End of life
- Maintenance
To find new Parkinson's treatments, we need people of all ages, genders and ethnicities to take part in research. By sharing opportunities with your patients, you'll help us find better treatments faster. And you'll help them gain a sense of purpose, community and control right now.
Whether you’re looking for leaflets to share or want to boost your research conversation skills, we have the tools to support you.
Got 5 minutes?
Get updates on the latest Parkinson's research news, events and research opportunities to share with patients.
Our introductory leaflet helps Parkinson's patients understand what research involves, the benefits of participating, and how to get involved.
Got 10 minutes?
Match research trials to your patient’s stage
Research participation ranges from quick questionnaires at home to trialling new treatments at a local hospital. Guide your patients toward an opportunity that matches their current journey.
A clinical trial called TOP HAT testing a treatment for Parkinson's-related hallucinations.
A clinical trial called EJS ACT-PD evaluating different repurposed drugs to slow progression.
A clinical trial testing a new drug to slow progression for medication-naive patients.
Remote genetic screening to identify candidates for future precision trials.
Got 30 minutes?
Learn how to lead research conversations
Boost your skills on your own schedule. Designed for all health and care professionals, this free, self-directed course gives you the tools to discuss research value, answer patient questions, and champion diverse participation in Parkinson's studies.
Get in touch
If you or your patients have any questions, please get in touch with our Research team. Email [email protected] or phone 020 7963 3606.