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NCT04046055

Cerebellar Transcranial Direct Current Stimulation in Parkinson's Disease

Completed NA Results posted Last updated 10 November 2022
What this trial tests

NA trial testing Transcranial direct current stimulation at 2 mA in Parkinson Disease in 7 participants. Completed in 1 April 2020.

Timeline
1 December 2019
Primary endpoint
1 April 2020
1 April 2020

Quick facts

Lead sponsorThorsten Rudroff
PhaseNA
StatusCompleted
Study typeINTERVENTIONAL
Allocationna
Designsequential
Maskingnone
Primary purposetreatment
Enrollment7
Start date1 December 2019
Primary completion1 April 2020
Estimated completion1 April 2020
Sites1 location across United States

Drugs / interventions tested

Conditions studied

Sponsor

Thorsten Rudroff

Who can join

Adults 50 to 90, any sex, with Parkinson Disease or Brain Stimulation. Patients with the condition only — healthy volunteers not accepted.

Results — posted to ClinicalTrials.gov

Per-arm endpoint measurements with 95% confidence intervals where reported. Source: trial results section.

Speed Walked During 30 Meter Walk Test Primary · 10 minutes

Walk as fast and as safe as possible over 30 meter

GroupValue95% CI
Sham 4 mA5.63± 0.84
Unilateral 2 mA5.65± 1.04
Bilateral 2 mA5.77± 1.07
Unilateral 4 mA5.86± 1.06
Bilateral 4 mA5.77± 1.24
Time to Complete the Timed Up and Go Test Primary · 10 minutes

From a seated position, stand up, walk 5 meters, turn around, walk back, and sit back down in the chair.

GroupValue95% CI
Sham11.9± 2.7
Unilateral 2 mA12.43± 2.32
Bilateral 2 mA12.80± 2.42
Unilateral 4 mA12.42± 2.72
Bilateral 4 mA12.70± 3.28
Movement of the Center of Pressure (2D; Forward-backward, Left-right) While Standing on a Firm Surface (Force Platform) for 1 Minute Primary · 1 minute

Stand as still as possible on a firm surface for 1 minute with the eyes open. Calculate the area of an ellipse that contains 95% of the 2D trace of the center of pressure movement.

GroupValue95% CI
Sham3.22± 2.56
Unilateral 2 mA2.47± 2.34
Bilateral 2 mA1.72± 0.50
Unilateral 4 mA1.60± 0.74
Bilateral 4 mA1.57± 0.39
Movement of the Center of Pressure (2D; Forward-backward, Left-right) While Standing on a Foam Surface (6 cm Foam Pad Placed on Top of Force Platform) for 1 Minute Primary · 1 minute

Stand as still as possible on a foam surface for 1 minute with the eyes open. Calculate the area of an ellipse that contains 95% of the 2D trace of the center of pressure movement.

GroupValue95% CI
Sham8.34± 7.57
Unilateral 2 mA7.53± 4.35
Bilateral 2 mA9.36± 6.90
Unilateral 4 mA8.30± 6.40
Bilateral 4 mA7.60± 3.63
Movement of the Center of Pressure (1D; Forward-backward) While Standing on a Firm Surface (Force Platform) for 1 Minute Secondary · 1 minute

Stand as still as possible on a firm surface for 1 minute with the eyes open.

GroupValue95% CI
Sham2.38± 0.70
Unilateral 2 mA2.90± 0.91
Bilateral 2 mA2.25± 0.62
Unilateral 4 mA2.25± 0.69
Bilateral 4 mA2.86± 1.02
Movement of the Center of Pressure (1D; Left-Right) While Standing on a Firm Surface (Force Platform) for 1 Minute Secondary · 1 minute

Stand as still as possible on a firm surface for 1 minute with the eyes open.

GroupValue95% CI
Sham2.1± 1.8
Unilateral 2 mA1.4± 0.6
Bilateral 2 mA1.3± 0.3
Unilateral 4 mA1.1± 0.4
Bilateral 4 mA1.1± 0.4
Movement of the Center of Pressure (1D; Forward-backward) While Standing on a Foam Surface (6 cm Foam Pad Placed on Top of Force Platform) for 1 Minute Secondary · 1 minute

Stand as still as possible on a foam surface for 1 minute with the eyes open.

GroupValue95% CI
Sham4.4± 2.8
Unilateral 2 mA4.0± 1.1
Bilateral 2 mA4.5± 1.8
Unilateral 4 mA4.11± 1.41
Bilateral 4 mA4.08± 1.19
Movement of the Center of Pressure (1D; Left-Right) While Standing on a Foam Surface (6 cm Foam Pad Placed on Top of Force Platform) for 1 Minute Secondary · 1 minute

Stand as still as possible on a foam surface for 1 minute with the eyes open.

GroupValue95% CI
Sham3.6± 1.8
Unilateral 2 mA3.4± 1.0
Bilateral 2 mA3.3± 1.3
Unilateral 4 mA3.3± 1.2
Bilateral 4 mA3.3± 1.0

Sponsor's own description

Parkinson's disease (PD) is the second most common neurodegenerative disorder and affects approximately 1 million people in the United States with total annual costs approaching 11 billion dollars. The most common symptoms of PD are tremor, stiffness, slowness, and trouble with balance/walking, which lead to severe impairments in performing activities of daily living. Current medical and surgical treatments for PD are either only mildly effective, expensive, or associated with a variety of side-effects. Therefore, the development of practical and effective add-ons to current therapeutic treatment approaches would have many benefits. Transcranial direct current stimulation (tDCS) is a non-invasive brain stimulation technique that can affect brain activity and can help make long-term brain changes to improve functions like walking and balance. While a few initial research studies and review articles involving tDCS have concluded that tDCS may improve PD walking and balance, many results are not meaningful in real life and several crucial issues still prevent tDCS from being a useful add-on intervention in PD. These include the selection of stimulation sites (brain regions stimulated) and tDCS electrode placement. Most studies have targeted the motor cortex (brain region that controls intentional movement), but there is evidence that the cerebellum - which helps control gait and balance, is connected to several other brain areas, and is easily stimulated with tDCS - may be a likely location to further optimize walking and balance in PD. There is also evidence that certain electrodes placements may be better than others. Thus, the purpose of this study is to determine the effects of cerebellar tDCS stimulation using two different placement strategies on walking and balance in PD. Additionally, although many tDCS devices are capable of a range of stimulation intensities (for example, 0 mA - 5 mA), the intensities currently used in most tDCS research are less than 2 mA, which is sufficient to produce measurable improvements; but, these improvements may be expanded at higher intensities. In the beginning, when the safety of tDCS was still being established for human subjects, careful and moderate stimulation approaches were warranted. However, recent work using stimulation at higher intensities (for example, up to 4 mA) have been performed in different people and were found to have no additional negative side-effects. Now that the safety of tDCS at higher intensities is better established, studies exploring the differences in performance between moderate (i.e., 2 mA) and higher (i.e., 4 mA) intensities are necessary to determine if increasing the intensity increases the effectiveness of the desired outcome. Prospective participants will include 10 people with mild-moderate PD that will be recruited to complete five randomly-ordered stimulation sessions, separated by at least 5 days each. Each session will involve one visit to the Integrative Neurophysiology Laboratory (INPL) and will last for approximately one hour. Data collection is expected to take 4-6 months. Each session will include walking and balance testing performed while wearing the tDCS device. Total tDCS stimulation time for each session will be 25 minutes.

Publications & conference data

1 peer-reviewed publication reference this trial (live from Europe PMC):

  1. Cerebellar Transcranial Direct Current Stimulation in People with Parkinson's Disease: A Pilot Study.
    Workman CD, Fietsam AC, Uc EY, Rudroff T. · · 2020 · cited 37× · PMID 32053889 · DOI 10.3390/brainsci10020096

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Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT04046055.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing