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Behavioural Intervention
Cerebellar transcranial direct current stimulation at 4 mA for Parkinson's Disease
N/A
Waitlist Available
Led By Craig D Workman, PhD
Research Sponsored by University of Iowa
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up through study completion, up to 12 months
Awards & highlights
Study Summary
Multiple Sessions of Transcranial Direct Current Stimulation in People With Parkinson's Disease
Eligible Conditions
- Parkinson's Disease
- Healthy Adults
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ through study completion, up to 12 months
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~through study completion, up to 12 months
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Primary outcome measures
30-meter walk test, dual-task (30mWT-DT; 2 trials)
30-meter walk test, single-task (30mWT-ST; 2 trials)
6-minute walk test (6MWT; 1 trial)
+9 moreSecondary outcome measures
Brain activity PET Imaging with [18F]Fluorodeoxyglucose (FDG)
Trial Design
4Treatment groups
Experimental Treatment
Active Control
Placebo Group
Group I: PD-ctDCSExperimental Treatment1 Intervention
People with Parkinson's disease will have both electrodes placed 1-2 cm below and 3 cm to either side of the inion, with the anode assigned to the most PD-affected side and the cathode assigned to the less PD-affected side. Stimulation is ramped up to 4 mA over the first 30 seconds and stays at 4 mA for the remainder of the stimulation time.
Group II: NH-ctDCSActive Control1 Intervention
Neurologically healthy older adults will have both electrodes placed 1-2 cm below and 3 cm to either side of the inion, with the anode assigned to the most PD-affected side and the cathode assigned to the non-dominant side. Stimulation is ramped up to 4 mA over the first 30 seconds and stays at 4 mA for the remainder of the stimulation time.
Group III: PD-shamPlacebo Group1 Intervention
People with Parkinson's disease will have both electrodes placed 1-2 cm below and 3 cm to either side of the inion, with the anode assigned to the most PD-affected side and the cathode assigned to the less PD-affected side. Stimulation is turned on (4 mA) for 30 seconds at the beginning and the end of the trial, but it turned to 0 mA in the intervening time.
Group IV: NH-shamPlacebo Group1 Intervention
Neurologically healthy older adults will have both electrodes placed 1-2 cm below and 3 cm to either side of the inion, with the anode assigned to the most PD-affected side and the cathode assigned to the non-dominant side. Stimulation is turned on (4 mA) for 30 seconds at the beginning and the end of the trial, but it turned to 0 mA in the intervening time.
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Who is running the clinical trial?
University of IowaLead Sponsor
447 Previous Clinical Trials
879,722 Total Patients Enrolled
Craig D Workman, PhDPrincipal InvestigatorUniversity of Iowa
2 Previous Clinical Trials
42 Total Patients Enrolled
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