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Study identifier: NCT06174948 Synced from ClinicalTrials.gov · July 29, 2026
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The Use of the CUE1/CUE1+ in People With Parkinson's Disease and Related Disorders

Condition: Parkinson's Disease and Parkinsonism · Progressive Supranuclear Palsy · Different Types of Tremor Including Essential Tremor  ·  Sponsor: Queen Mary University of London

PhaseNA
Planned participants70
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersNo

About this study

People with Parkinson's disease (PD) commonly experience a range of both motor (e.g., bradykinesia, rigidity, tremor, and postural instability) and non-motor (e.g., fatigue, psychiatric and behavioural disturbances, autonomic dysfunction, cognitive impairment, sleep dysfunction and olfactory loss) features. Currently, it is challenging to alleviate these symptoms with first-line treatment, the medications such as levodopa. The CUE1 is a non-invasive device, which is approved for sale in the UK market as a Class I low risk device. It is worn on the sternum or other part of the body such as the forearm and attaches to the skin via an adhesive patch which has been dermatologically tested and approved. The CUE1 delivers pulsing cueing and vibrotactile stimulation to help improve symptoms in people with PD and it has shown to be effective in doing so in previous small case studies. This 9-week feasibility study aims to investigate the feasibility, safety, tolerability and effect of using the CUE1 as an intervention to improve motor and non-motor symptoms in people with PD and related movement disorders. People with clinical diagnosis of idiopathic PD and related disorders including those with progressive supranuclear palsy, multiple system atrophy, corticobasal degeneration, orthostatic tremor and vascular Parkinsonism as well as atypical dystonias and tremor disorders aged over 18 years old who have the capacity to provide a written consent form to take part in the study, will r…

This description comes directly from the study's public registry record.

Talk to the study team

Cristina Simonet, PhD  ·  020 7882 3543  ·  c.simonet@qmul.ac.uk

Viktoria Azoidou, PhD  ·  020 7882 3850  ·  v.azoidou@qmul.ac.uk

Always discuss trial participation with your own doctor first.

Locations (1)

Queen Mary University of LondonLondon, United KingdomRecruiting

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Source record: clinicaltrials.gov/study/NCT06174948