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Effects of Transcranial Direct Current Stimulation on Fine Motor Skills in Parkinson's Disease: a Pilot Study

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02287207
Enrollment
20
Registered
2014-11-10
Start date
2015-10-31
Completion date
2016-04-30
Last updated
2016-06-08

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Fine Motor Skills, Handwriting, Parkinson's Disease, Transcranial Direct Current Stimulation

Brief summary

The purpose of this pilot study is to determine the effect of transcranial direct current stimulation (tDCS) on brain activity and fine motor skills in patients with Parkinson's disease compared to healthy controls.

Detailed description

The pilot study will involve a double-blind, sham controlled cross-over design where participants will receive anodal and sham tDCS stimulation in a randomized order. Differences in brain activity and fine motor skill performance between groups and after tDCS stimulation will be compared.

Interventions

DEVICEtranscranial direct current stimulation (tDCS)

Sponsors

KU Leuven
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
TREATMENT
Masking
SINGLE (Subject)

Eligibility

Sex/Gender
ALL
Healthy volunteers
Yes

Inclusion criteria

* Diagnosed with idiopathic PD, according to the UK Brain Bank criteria * Hoehn and Yahr (H&Y) stage II in the 'on'-phase of the medication cycle * Right dominant PD

Exclusion criteria

* Cognitive impairment (MMSE \< 23) * Visuo-spatial deficits (measured by the Rey-Osterrieth Complex Figure (ROCF) test) * Left-handedness (evaluated by the Edinburgh Handedness scale) * Depression * Pregnancy * Alcohol abuse * Aneurysm clips * Pacemaker * Neurostimulator * Implemented defibrillator * Magnetically activated implant or device * Implemented pump * Spinal cord simulator * Implemented hearing aid * Artificial or prosthetic limb * Metal parts in the body * Any external or internal metal * Artificial heart valve * Other implants * History of brain surgery * Migraine * Family history of Epilepsy * Other contra-indications for tDCS and Transcranial Magnetic Stimulation (TMS) * Other neurological, psychiatric or interfering upper limb problems

Design outcomes

Primary

MeasureTime frameDescription
Change in writing amplitudepost-stimulation (immediately after) and retention (1 week)Centimeter (cm)
Change in writing velocitypost-stimulation (immediately after) and retention (1 week)Centimeter per second (cm/s)

Secondary

MeasureTime frameDescription
Change in speed on the Purdue Pegboard taskpost-stimulation (immediately after) and retention (1 week)Number of pegs placed in 30 seconds
Change in cortical excitabilitypost-stimulation (immediately after) and retention (1 week)Motor Evoked Potentials (MEP) peak to peak amplitude and latency - Measured with single-pulse Transcranial Magnetic
Change in Short-Latency Intracortical Inhibition (SICI)post-stimulation (immediately after) and retention (1 week)Measured with double-pulse Transcranial Magnetic Stimulation (TMS)
Change in cortical silent period (cSP)post-stimulation (immediately after) and retention (1 week)Measured with single-pulse Transcranial Magnetic

Countries

Belgium

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026