Actively Recruiting

Phase Not Applicable
All Genders
ID06883266

Transcranial Direct Current Stimulation to Improve Motor Function and Motor Fatigue in Parkinson's Patients

Led by Sanford Health · Updated on 2026-02-03

64

Participants Needed

1

Research Sites

4 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Parkinson's disease (PD) is a common and rapidly growing neurodegenerative disorder characterized by impaired motor function, including bradykinesia, motor fatigue, and motor fatigability. These symptoms significantly affect the quality of life for people with PD. Researchers are evaluating whether multiple sessions of anodal transcranial direct current stimulation (atDCS) applied to the left primary motor cortex (M1) can improve motor function and reduce motor fatigue and fatigability in PD patients. Participants will be assigned to one of two groups: an experimental group receiving 2 milliamps (mA) of anodal transcranial direct current stimulation (tDCS) for 20 minutes daily over 5 consecutive days, and a sham group receiving only a brief 30-second stimulation ramp-up with no further stimulation during the 20-minute sessions. Both groups will have electrode placement at the left dorsolateral prefrontal cortex. The study will examine if the treatment effects last up to two weeks following the final session. Throughout the study, participants will undergo multiple assessments including finger and toe tapping tests using the KinesiaOne device at baseline, after the 5-day treatment, and at follow-up visits 7 and 14 days later. Additional evaluations include cognitive testing (MOCA), fatigue questionnaires (Multidimensional Fatigue Inventory), depression scales (CES-D), quality of life assessments (McGill QOL Scale), and motor symptom reports (MDS-UPDRS Part II). These assessments help measure changes in motor function, fatigue, cognition, mood, and quality of life over the study period.

CONDITIONS

Brief Title

Transcranial Direct Current Stimulation for Motor Function and Fatigue in PD

Who Can Participate

All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Clinical diagnosis of Parkinson's disease with at least two of these symptoms: tremor, rigidity, bradykinesia, or postural instability
  • Ability to provide informed consent
Not Eligible

You will not qualify if you...

  • Diagnosis of dementia with a MOCA score below 21
  • Previous treatment with deep brain stimulation (DBS) for Parkinson's disease
  • Diagnosis of psychosis
  • Diagnosis of multiple sclerosis
  • Diagnosis of stroke
  • Diagnosis of chronic obstructive pulmonary disease (COPD)
  • Diagnosis of congestive heart failure (CHF)

AI-Screening

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 screening and enrollment visit

Implementation

Duration - 5 consecutive days

Participants receive transcranial direct current stimulation (tDCS) or sham stimulation daily for 20 minutes over 5 consecutive days.

5 daily visits (in-person)

Follow-up

Duration - 14 days

Participants are assessed for motor function and fatigue at 7 and 14 days after the last stimulation session to evaluate lasting effects.

2 follow-up visits (in-person)

Trial Site Locations

Total: 1 location

1

Sanford Brain and Spine Center

Fargo, North Dakota, United States, 58103

Actively Recruiting

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Research Team

J

Jessica Keller, B.S.

How is the study designed?

Study Type

INTERVENTIONAL

Masking

DOUBLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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Published Research Related To This Trial

Clinical research with transcranial direct current stimulation (tDCS): challenges and future directions.

Andre Russowsky Brunoni, Michael A Nitsche, Nadia Bolognini...

https://pubmed.ncbi.nlm.nih.gov/22037126