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Testing electrical brain stimulation for thinking difficulties

Researchers study whether electrical stimulation applied through the head affects thinking abilities in Parkinson’s.

Testing a treatment or activity · Study reference: NCT03025334

Plain-language introduction written with AI from the registry; not independently checked by a clinician. Read the original details below ↓

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Looking for volunteers

Start (reported actual date)
2017-03-22
Main measurements finished (planned)
2027-08-31
Study finished (planned)
2027-08-31

Planned dates can move. A study finishing does not tell us when a paper will be published.

No results summary has been confirmed in the registry records we imported. See connected papers below; we keep checking after recruitment ends.

Changes we have recorded
  • 2026-10-11 — recruiting

These are dates we observed a change, not necessarily the dates it happened.

Papers connected to this study

No connected paper has been found yet. The tracker checks the growing library for study identifiers and registry-linked publications.

Who can join?

Age 40 years and over · Does not accept healthy volunteers

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Read all the rules for taking part

Sex eligibility reported by registry: all

Inclusion Criteria: * Patients must meet diagnostic criteria for idiopathic Parkinson's disease, defined as the presence of two or more of the cardinal clinical features of PD in the absence of known causes of parkinsonism such as encephalitis or neuroleptic treatment * Ability to provide written informed consent * defined by the Diagnostic and Statistical Manual of Mental Disorders; DSM-5) * Age \> 40 * fluent in English. * Patients' cognitive statuses will be evaluated by the participating neuropsychiatrist or a trained psychiatry or neurology resident. Exclusion Criteria: * Patients with dementia (defined as a Montreal Cognitive Assessment score \< 18) * Atypical parkinsonian features including myoclonus, apraxia, oculomotor abnormalities, ataxia, sensory loss, or pyramidal signs. * Abnormal MRI * metal implants or a cardiac pacemaker * Pregnant or breastfeeding women (female subjects of child bearing potential will be screened for pregnancy before MRI imaging). * severe dyskinesia that may interfere with the quality of the scan (e.g., dyskinesia involving head movement). * severe hypertension. * cardiovascular disease. * Patients with a history of seizure, stroke, moderate to severe head injury, high intracranial pressure, severe headaches, or presence of other neurologic disease that may be associated with an altered seizure threshold; or concurrent medication use, such as tricyclic antidepressants, neuroleptic medications, or other drugs that are known to lower seizure threshold * secondary conditions that may significantly alter electrolyte balance or lower seizure threshold. * Family history of epilepsy.
Full study name & original research details

Official study title

Transcranial Direct Current Stimulation Treatment of Cognitive Dysfunction in Parkinson's Disease

Short title used by the registry

tDCS on Parkinson's Disease Cognition

Original description

Parkinson's disease (PD) has been classically regarded as a "movement disorder", so earlier work has focused on treating motor symptoms only. As PD patients now have longer life expectancy, the relatively slowly progressing cognitive deficits (compared to their motor deficits) have become one of the major challenges. Approximately 80% of PD patients eventually become demented. Therefore cognitive dysfunction is one of the most significant factors affecting the quality of life of patients with PD. While dementia in Parkinson's disease is routinely treated by cholinesterase inhibitors (e.g., donepezil and rivastigmine), their efficacy on mild cognitive impairment found in non-demented PD is questionable. Alternative approaches have been proposed including transcranial direct current stimulation (tDCS) but no consensus has been reached. This can be attributed mainly to: (1) imprecise knowledge of the underlying functional circuitry mediating this disease manifestation and (2) inter-individual variability. Here, the investigators will utilize a novel personalized network analysis approach to elucidate on the underlying mechanisms of the effect of tDCS on cognitive dysfunction in non-demented PD patients. It has been well documented that the caudate nucleus plays an important role in cognitive dysfunction found in PD. In the investigators' preliminary resting-state functional magnetic resonance imaging (fMRI) study, they have shown that the connectivity of the right caudate nucleus is correlated to cognitive status of PD patients measured by the Montreal Cognitive Assessment (MoCA). The investigators hypothesize that tDCS on the left and/or right dorsolateral prefrontal cortex may restore the functional connectivity of the right caudate nucleus which may in turn improve patients' cognitive performance.

Conditions reported: Parkinson Disease; Mild Cognitive Impairment

Registry records for this study

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Study type
Interventional
Interventions
High-definition transcranial direct current stimulation
Phases
NA
Sponsor
University of Manitoba
Start date reported by registry
2017-03-22 (actual)

Registry updated: 2026-05-01 · Status last verified by the registry submitter: 2026-04

Registry records retrieved 2026-10-11 (UTC). Individual records may have older updates. Recruitment and eligibility must be confirmed with the study team.

Contact the research team

Public study contacts supplied to the registry. Ask whether recruitment is still open and what participation involves.

Ji Hyun Ko, PhD · 204-318-2566 · ji.ko@umanitoba.ca

Study locations

Site status can differ from overall study status. “Status not reported” means local availability needs confirmation. Remote participation and travel arrangements must be checked with the team.

University of Manitoba

Winnipeg, Manitoba, Canada

Recruiting

Ji Hyun Ko, PhD · 204-318-2566 · ji.ko@umanitoba.ca

Facility not reported

Canada

Status not reported

The original descriptions and participation rules come from the registry. Participation is voluntary and does not guarantee benefit.