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The Cerebral Mechanisms of Re-emergent Tremor in Parkinson's Disease

The Cerebral Mechanisms of Re-emergent Tremor in Parkinson's Disease - RET-PD

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
NL-OMON
Registry ID
NL-OMON57007
Enrollment
40
Registered
2024-04-09
Start date
2025-02-26
Completion date
Unknown
Last updated
2026-06-01

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Parkinson's disease

Interventions

Sponsors

Radboud Universitair Medisch Centrum
Lead Sponsor

Eligibility

Age
18 Years to 99 Years

Inclusion criteria

Inclusion criteria:  - A diagnosis of idiopathic PD made by a movement disorder specialist - PD disease duration of 7 years or less, defined as time since diagnosis by a  neurologist - A history of both resting and re-emergent postural tremor in the same arm 

Exclusion criteria

Exclusion criteria:  - Severe neurological co-morbidity - Co-existing other tremor (e.g., functional tremor, dystonic tremor, essential  tremor) - Significant cognitive impairment: Montreal Cognitive Assessment (MoCA) <21  points - Contra-indications for MRI - Moderate to severe head tremor - Tremor latency duration >20 seconds after abrupt voluntary movement - Unclear tremor suppression after voluntary movement - Taking dopamine-agonists with a levodopa equivalent dose of more than 150mg  per day 

Design outcomes

Primary

MeasureTime frame
Re-emergent postural tremor-related cerebral activity, as measured by combined electrophysiology-fMRI. This robust technique has already been widely applied to several different tremor syndromes, including Parkinsonian resting tremor, essential tremor, and dystonic tremor

Secondary

MeasureTime frame
Clinical assessments: disease severity using MDS-UPDRS Part III (motor examination), most-affected side, most-tremulous side, handedness (Edinburgh Handedness Inventory), and cognitive function (MoCA). Structural MRI: T1 and T2-weighted structural images, diffusion-tensor imaging (DTI) scan, and neuromelanin scan. The anatomical T1-image will be used for registration of the fMRI-scans and the T2-image for improved cerebellar segmentation. The DTI and neuromelanin scans will be used to look for the integrity of the substantia nigra and locus coeruleus (LC). These measures are then correlated to clinical and electrophysiological tremor characteristics, as well as cerebral tremor-related activity (see below). Functional MRI: the fMRI experiment will be used to investigate and localize cerebral tremor-related activity. Moreover, within-subject differences in cerebral activity patterns and connectivity strengths between resting tremor and re-emergent postural tremor will be investigated. The extent of activity and effective connectivity parameters of the tremor-circuit will be correlated with electrophysiological tremor characteristics (e.g., tremor amplitude, the duration of the latency, etc). Electrophysiology: tremor will be measured from surface-electromyography (EMG) and accelerometery. Surface EMG electrodes will be placed on the first dorsal interosseus, abductor pollicis brevis, extensor carpi radialis, flexor carpi radialis, biceps, and triceps on the most-tremulous side. In case of clear leg tremor, surface EMG-electrode may be placed on the gastrocnemius and/or tibialis anterior muscles. A tri-axial accelerometer will be placed on both the most and least-tremulous side (dorsum of the hand). These peripheral tremor measures will be used to characterize tremor, assess tremor-specific eligibility for the fMRI session, and during scanning to compute scan-by-scan fluctuations of tremor power, which will be used to obtain cerebral tremor-related activity, as done

Countries

Netherlands

Contacts

Public ContactR.C.G. Helmich

Radboud Universitair Medisch Centrum

rick.helmich@radboudumc.nl0650155762

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP) · Data processed: Jun 11, 2026