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Clinical Trial Summary

The purpose of this single arm study is to evaluate the feasibility and safety of treatments with a non-invasive neuromodulation device in adults diagnosed with mild/moderate Parkinson's disease dementia (PDD). A non-invasive device is a device that stays outside of the body and is not implanted and does not penetrate the skin. Neuromodulation means that the device stimulates activity in the brain.


Clinical Trial Description

Up to 12 participants will self-administer treatments twice daily in the home setting over a period of 12 weeks. There are 4 study center visits, including an eligibility visit, as well as multiple phone calls. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05987540
Study type Interventional
Source Scion NeuroStim
Contact Kara Richardson
Phone 984-884-1020
Email krichardson@scionneurostim.com
Status Recruiting
Phase N/A
Start date May 8, 2024
Completion date November 1, 2025

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