The assessment of the quality of movement control in patients with Parkinson*s disease receiving deep brain stimulation.

Completed

• Conditions: Parkinson's disease; 10028037

• Registration Number: NL-OMON30995
• Lead Sponsor: Medisch Spectrum Twente

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Last Update Posted: 13 May 2024

Recruitment & Eligibility

• Status: Completed
• Sex: Not specified
• Target Recruitment: 10

Inclusion Criteria

- Parkinson patients having a deep brain stimulator in the subthalamic nucleus
- Patients experiencing a good clinical result from DBS
- Patients having no major fluctuations in symptoms due to medication
- Patients being in good physical condition
- Patients responding within 5 minutes to changes in the stimulator settings

Exclusion Criteria

- Patients not being able to fully cooperate with the experiments
- Patients suffering from dementia
- Patients suffering from severe dyskinesia

Study & Design

• Study Type: Observational non invasive
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
<p>Parameters (obtained from the inertial sensors) relating to the UPDRS-scores<br /><br>for tremor, bradykinesia, and akinesia during three conditions are compared.<br /><br>These conditions are stimulator on with normal settings, stimulator on with<br /><br>altered settings, and stimulator off.<br /><br>The correlations of these parameters to the UPDRS-scores of tremor,<br /><br>bradykinesia, and akinesia is also assessed.</p><br>

Secondary Outcome Measures

Name	Time	Method
<p>not applicable</p><br>