This investigation is undertaken to:
* Evaluate the accuracy and reliability of the device in measuring and recording motor symptoms associated with Parkinson's Disease (PD), and
* To assess the safety and tolerability of the device in patients with PD.
Trial Locations
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Eligibility Criteria
Inclusion Criteria:
1. Parkinson disease: Clinically diagnosed
2. Age ≥ 50 (not in the childbearing aged as defined by Statistics Denmark, 15-49)
3. Experiencing at least two of following symptoms and/or side effect on a daily basis:
* Rigidity
* Tremor
* Bradykinesia
* Dyskinesia (tre…
Inclusion Criteria:
1. Parkinson disease: Clinically diagnosed
2. Age ≥ 50 (not in the childbearing aged as defined by Statistics Denmark, 15-49)
3. Experiencing at least two of following symptoms and/or side effect on a daily basis:
* Rigidity
* Tremor
* Bradykinesia
* Dyskinesia (treatment side effect)
4. Provision of informed consent, i.e., the subject must be able to:
* Read and understand the Patient Information and Consent Form
* Sign the Patient Information and Consent Form.
Exclusion Criteria:
1. Known allergy/hypersensitivity to any material in direct contact with the skin (stainless steel, silicone and polyester)
2. MMSE \<24
3. Other neurological diseases
Contacts
No contact information available.
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