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Clinical Trials/NCT02104401
NCT02104401
Completed
Phase 1

Pilot Study: Open Label Treatment With tDCS for Parkinson's and Related Disorders for Improvement of Speech, Gait and Mood

Georgetown University1 site in 1 country10 target enrollmentOctober 2013

Overview

Phase
Phase 1
Intervention
Not specified
Conditions
Parkinson's Disease
Sponsor
Georgetown University
Enrollment
10
Locations
1
Primary Endpoint
Improvement of Motor and Speech Symptoms of Parkinson's Disease or Related Disorders
Status
Completed
Last Updated
11 years ago

Overview

Brief Summary

This research will help us to understand whether transcranial direct current stimulation (tDCS) can safely improve recovery of speech and language abilities, gait , and mood in people with Parkinson's disease and related disorders. Some of the disorders that will be studied to understand if tDCS can be useful include Parkinson's Disease, Multi-System Atrophy (MSA) and progressive supranuclear palsy (PSP).

Registry
clinicaltrials.gov
Start Date
October 2013
End Date
March 2014
Last Updated
11 years ago
Study Type
Interventional
Study Design
Single Group
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Parkinson's disease or a related disorder (e.g. Multiple Systems Atrophy) as diagnosed by a neurologist specializing in Movement Disorders
  • Age \>= 18 years

Exclusion Criteria

  • Skull defect at or near site of tDCS delivery.
  • History of a significant stroke or traumatic brain injury.
  • History of other brain conditions that could impact interpretation of results (such as MS, brain tumor, encephalitis).
  • Presence of implanted electrical or metallic devices in the head or body (examples include cardiac pacemakers or defibrillators, Baclofen pumps, deep brain stimulators, ventricular shunts with metallic parts, vagus nerve stimulators)
  • Presence of ferrous metal in the head (except titanium; for instance shrapnel)
  • History of psychiatric disease requiring hospitalization, electroconvulsive therapy, or ongoing medication use (other than common antidepressants)
  • Pregnancy

Outcomes

Primary Outcomes

Improvement of Motor and Speech Symptoms of Parkinson's Disease or Related Disorders

Time Frame: 16 weeks

We will perform an assessment of motor function using Part III of the Unified Parkinson's Disease Rating Scale (UPDRS), timed test of gait, and patient self-assessment. Speech functions will be assessed with sentence repetition,evaluation of spontaneous speech, and other standard language tests. The assessment will also include other measures and questionnaires (e.g. Bech Depression Inventory) to be filled out by the patient and his/her family.

Secondary Outcomes

  • Improvement of Neuropsychiatric Symptoms of Parkinson's Disease or Related Disorders(16 weeks)

Study Sites (1)

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