The Effects of Multi-focal tDCS on Motor-cognitive Dysfunctions in Parkinson's Disease

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

UNKNOWN

Clinical Phase

NA

Total Enrollment

85 participants

Study Classification

INTERVENTIONAL

Study Start Date

2017-01-31

Study Completion Date

2020-01-31

Brief Summary

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The current RCT aims to establish the therapeutic potential of tDCS for freezing of gait (FOG) and motor-cognitive dysfunctions in PD. As noted, FOG is often unresponsive to pharmacological and other treatments, especially in the advanced stages of the disease. While it is likely that tDCS will provide symptomatic relief, we will also explore, via secondary outcomes, the potential for tDCS to modify disease progression. Support for this possibility stems from the likely mechanisms of action of tDCS.

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Detailed Description

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The current study aim to establish the therapeutic potential of tDCS for freezing of gait (FOG) and motor-cognitive dysfunctions in Parkinson's Disease (PD). FOG phenomenon is often unresponsive to pharmacological and other treatments, especially in the advanced stages of the disease. While it is likely that Transcranial direct current stimulation (tDCS) will provide symptomatic relief, we will also explore, via secondary outcomes, the potential for tDCS to modify disease progression. Support for this possibility stems from the likely mechanisms of action of tDCS.

Based on strong rationale and preliminary findings in previous works, the objectives of the current proposal are to conduct a prospective multi-center, double-blinded, stratified controlled randomized clinical trial, comparing real multifocal tDCS to sham stimulation. The main aim:

\- To demonstrate the "short-term" and the longer-term effects of tDCS on FOG severity and frequency.

Participants: A total of 85 patients will be recruited (Hoehn and Yahr Stage 1-3.5) who suffer from FOG, as measured by the new FOG questionnaire (NFOG-Q) and as demonstrated in response to a FOG provoking protocol, who are on stable medications, who have no contraindications to tDCS, and who are between the ages of 40-80. Patients with DBS will not be included.

tDCS intervention: Subjects will be randomized to receive either a real or sham tDCS intervention. Each intervention will consist of 10, 20-minute treatments completed over 2 consecutive weeks (i.e., 5 per week), following previously established protocols. A single, weekly "maintenance" treatment will then be provided for the following 12 weeks (note: for depression, maintenance tDCS is most often provided once every two weeks; we will take a more conservative approach here in this first long-term study for FOG in PD).

Participants will continue taking their regular medications, and treatments will take place in the "ON" medication state (approximately at the same time of day for each treatment). The real tDCS intervention will simultaneously target both the M1 leg area and the the dorsolateral prefrontal cortex (DLPFC), in the brain hemisphere contralateral to the more affected side of the body, as determined by the summation of the motor symptoms on The unified Parkinson's disease rating scale (UPDRS). Current will be applied using an array of 8 sponge electrodes and the StarStim tDCS device and software (Neuroelectrics, Inc). For this protocol, the placement and current delivered through each electrode has been optimized using the Neuroelectrics StimWeaver® Stimulation Optimization Service . In case of bilateral symptom symmetry, tDCS will target the left M1 and DLPFC. For the sham intervention, the same electrode placement and stimulation parameters will be used; however, current will only be applied for the first 60 seconds of the stimulation session. This is a reliable control as sensations arising from tDCS diminish considerably after the first minute of stimulation. At the end of each treatment session, participants will complete a short questionnaire to assess potential side-effects. At the end of the entire intervention, participants will be asked to state if, in their opinion, they received the real or sham intervention.

Outcome measures: The primary outcome will be the number of FOG episodes measured in the lab when subjects undergo a validated FOG-invoking protocol, after the initial 2-week intervention and at the final study point, similar to that proposed by Ziegler et al. Briefly, this protocol includes situations that have been shown to provoke FOG. Patients will be asked to sit, to stand up and to walk to a a mark on the floor. They will perform two 360° turns, clockwise and counter-clockwise. Then, the patients will be asked to open a door and walk through it, turn outside, and come back to their chair. Secondary outcomes of FOG will include FOG duration and the new FOG questionnaire (NFOG-Q). This FOG-provoking protocol will take place in both the ON and OFF medication state and higher values (worse) of FOG will be used as the primary outcome measure (in secondary analyses, we will examine ON and OFF FOG separately).

Additional secondary measures will test the influence of tDCS on other motor, cognitive or motor-cognitive functions related to PD and FOG. Secondary outcomes related to motor function, which are likely to be affected by changes in M1 excitability, will include gait speed (usual walking), Timed Up \& Go scores, UPDRS motor scores, and level of activity over 7 days using portable, lightweight, water-proof sensors. Secondary measures of executive function, which are hypothesized to be responsive to tDCS of the DLPFC, will include the Trail Making test (TMT) parts A and B, and a previously validated computerized neuropsychological battery that provides normalized scores for executive function and attention (and memory). Dual-tasking gait speed (i.e., walking while performing a serial subtraction test) will assess motor-cognitive interactions. Functional near infra-red spectroscopy (available in Boston and Tel Aviv) will assess frontal activation during dual-tasking walking; this reflects the subjects ability to handle cognitive loading and has been associated with FOG. Finally, the PDQ-39 will evaluate quality of life.

Conditions

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Parkinson's Disease

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

TREATMENT

Blinding Strategy

TRIPLE

Participants Caregivers Investigators

Study Groups

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Active tDCS

The active tDCS condition will consist of 20 min of continuous stimulation. This amount of stimulation is safe for healthy young and older adults and has been shown to induce acute beneficial changes in cortical excitability and cognitive functions.

Group Type EXPERIMENTAL

Active tDCS

Intervention Type DEVICE

In this group subjects will receive 20 min of treatment.

Sham tDCS

The Sham tDCS - an inactive stimulation.

Group Type SHAM_COMPARATOR

Sham tDCS

Intervention Type DEVICE

In this group subjects will receive 20 min of sham stimulation.

Interventions

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Active tDCS

In this group subjects will receive 20 min of treatment.

Intervention Type DEVICE

Sham tDCS

In this group subjects will receive 20 min of sham stimulation.

Intervention Type DEVICE

Eligibility Criteria

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Inclusion Criteria

Inclusion Criteria:

Inclusion criteria: patients diagnosed with PD, with Hoehn and Yahr Stage between 1-3.5, who suffer from FOG, as measured at screening by the previously validated new FOG questionnaire (NFOG-Q), whose medications have not changed within 1 month of the study and are not anticipated to change during the study, are able to walk independently, and who are between the ages of 40-80 inclusive.

Exclusion Criteria:

Subjects who show no FOG during testing in the lab in response to a FOG provoking protocol, any diagnosed psychiatric or other neurological disorder, stroke, unbalanced and high blood pressure, pregnancy, participation in any clinical trial in the last three months, unwillingness to be randomized; implanted with deep brain stimulation, pacemakers, intracranial electrodes, implanted defibrillators or any other prosthesis; or a perceived inability to complete the study. Additional exclusion criteria related to tDCS safety will include a personal or family history of epilepsy, the use of neuro-active drugs, or risk of metal fragments in the eyes or head.

Minimum Eligible Age

25 Years

Maximum Eligible Age

90 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes