movement disorders shaking
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: - Newly implanted patient with the Medtronic Percept* PC neurostimulator, and diagnosed with Parkinson*s disease, tremor or dystonia (nb this can be during the first DBS lead implantation or during the repacement of the prior DBS neurostimulator). - Informed consent - Age 18 years or older
Exclusion criteria
Exclusion criteria: - Patients implanted with the Medtronic Percept* PC neurostimulator with other other indications than Parkinson's disease, tremor or dystonia - Patients implanted with a Medtronic DBS Pocket Adaptor Model 64001 or 64002. These DBS systems are not compatible with BrainSenseTM technology.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Primary end points per study part: Part A: correlation of disease specific neural oscillations ON and OFF stimulation (full-spectrum (0-125 Hz) recordings) with symptom severity. Part B: relation between neural oscillations with DBS switched ON and OFF, their interaction with symptom severity, and their stability during multiple measurements over time. Part C: relation between PD motor and non-motor symptoms, motivational state, smartwatch kinematics and neural oscillations over a 2-week at-home intervalrelation between the presence of disease | — |
Secondary
| Measure | Time frame |
|---|---|
| - | — |
Countries
Netherlands
Contacts
Amsterdam UMC