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Walking practice with electrical brain stimulation

This study tests stimulation through the scalp alongside task-based walking exercises for Parkinson's.

Testing a treatment or activity · Study reference: RBR-6bvnx6

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

This registry record was last updated over six months ago, or its update date is missing. Recruitment may have changed. Confirm with the team before making plans.

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Looking for volunteers

Start (reported date)
2019-09-01

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?

Ages 40y to 100y · Ask the team who can join

These are starting points, not the full rules. The research team can tell you whether the study is right for your situation.

Read all the rules for taking part

Sex eligibility reported by registry: -

Inclusion criteria: Participants will be individuals with Parkinson’s Disease, who will be eligible, if they: are over 40 years of age; are able to walk at least 14 meters, independently, with or without assistive devices; walk at speeds lower than 1.1 m/s; have experienced freezing episodes over the past month, according to the Part I of the New Freezing of Gait Questionnaire (Nieuwboer et al 2009); have adapted to their current anti-Parkinsonian medication for at least 2 weeks; provide written consent. Exclusion criteria: They will be excluded, if they: have cognitive deficits, which will be screened by the Mini-Mental State Examination. The cut-off scores are 26 for people with high levels of education, 18 for people with elementary and middle levels, and 13 for illiterate people (Bertolucci et al 1994);suffer from unstable cardiovascular disease or other uncontrolled chronic conditions that would interfere with the safety and conduct of the training and testing protocol or interpretation of the results; over 100 years of age.
Full study name & original research details

Official study title

Effect of the transcranial direct current stimulation (tDCS) associated with Physical Therapy on freezing of gait and functionality after Parkinson’s disease.

Short title used by the registry

Physical therapy to improve walking in people with Parkinson's Disease.

Original description

Intervention: 24 individuals will be recruited. The intervention is physical therapy including task-specific walking training associated with transcranial direct current stimulation (tDCS), 30 min per day, three days per week, over four weeks. A stimulator (DC-Stimulator Plus, NeuroConn, Ilmenau, Germany) will deliver a continuous direct current by a saline-soaked pair of surface sponge electrodes (size of electrodes 35cm2). The anode will be placed at the Cz position on the scalp, corressponding to the location of the supplementary motor area, in accordance with the International EEG 10/20 system (Klem et al 1999, Yotnuengnit et al 2018). The cathode will be positioned over the supraorbital area. Participants will receive electrical stimulation of 2 mA, during the walking training. The 30-min sessions of task-specific walking training will include practicing part of the task (about 10 min), where the muscles are working in a manner similar to a full task performance and practicing the whole task (about 20 min). The control group will undertake the task-specific walking training associated with a sham- tDCS. The control group will receive the same walking training, electrodes positioning and testing schedule as the experimental group. This will avoid bias related to type and amount of attention given to participants. If the addition of tDCS proves to be effective, the control group may receive the experimental training program after the experiment is complete. The intervention will be undertaken in Clinics of Physiotherapy at the Universidade Federal do Espírito Santo. To encourage the participants to comply with the protocol, both groups will be asked to sign a symbolic contract of commitment to the proposed protocol. 12 partcipants will be randomi;Other;E02.779;E02.331.800;E01.370.600.250 Primary outcome: The primary outcome is comfortable walking speed, measured by the 10-m Walk Test, and reported in m/s. Secondary outcome: Walking step length and cadence will be measured using the 10-m Walk Test. Step length will be calculated by dividing the covered distance, i.e., 10m, by the number of steps to cover the distance, and reported in meters. Walking cadence will be calculated by dividing the number of steps by the time to cover the distance, i.e., 10m, and reported in steps/min.;Walking confidence will be measured using the Brazilian version of the modified Gait Efficacy Scale, and reported as scores ranging from 10 to 100. ;Mobility will be measured by the Timed-up and Go Test (TUG) and reported as seconds. ;Freezing of gait will be measured using Parts II and III of the New Freezing of Gait Questionnaire, and reported as scores ranging from 0 to 28, where higher scores indicate worse episodes of freezing.;Fear of falling will be measured using the Brazilian version of the Falls Efficacy Scale – International (FES-I Brazil), and reported as scores ranging from 16 to 64, where higher scores indicate greater fear of falling. ;The number of falls will be recorded by the use of a “falls diary” , and the proportion of fallers in each group will also be compared.

Conditions reported: Parkinson Disease.;C10.228.140.079.862.500

Registry records for this study

Records are joined using registration identifiers. Titles alone do not establish that two studies are the same.

Study type
Interventional
Interventions
24 individuals will be recruited. The intervention is physical therapy including task-specific walking training associated with transcranial direct current stimulation (tDCS), 30 min per day, three days per week, over four weeks. A stimulator (DC-Stimulator Plus, NeuroConn, Ilmenau, Germany) will deliver a continuous direct current by a saline-soaked pair of surface sponge electrodes (size of electrodes 35cm2). The anode will be placed at the Cz position on the scalp, corressponding to the location of the supplementary motor area, in accordance with the International EEG 10/20 system (Klem et al 1999, Yotnuengnit et al 2018). The cathode will be positioned over the supraorbital area. Participants will receive electrical stimulation of 2 mA, during the walking training. The 30-min sessions of task-specific walking training will include practicing part of the task (about 10 min), where the muscles are working in a manner similar to a full task performance and practicing the whole task (about 20 min). The control group will undertake the task-specific walking training associated with a sham- tDCS. The control group will receive the same walking training, electrodes positioning and testing schedule as the experimental group. This will avoid bias related to type and amount of attention given to participants. If the addition of tDCS proves to be effective, the control group may receive the experimental training program after the experiment is complete. The intervention will be undertaken in Clinics of Physiotherapy at the Universidade Federal do Espírito Santo. To encourage the participants to comply with the protocol, both groups will be asked to sign a symbolic contract of commitment to the proposed protocol. 12 partcipants will be randomi;Other;E02.779;E02.331.800;E01.370.600.250
Phases
N/A
Sponsor
Universidade Federal do Espírito Santo
Start date reported by registry
2019-09-01 (reported)

Registry updated: Not reported · Status last verified by the registry submitter: Not reported

Registry records retrieved 2026-10-13 (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.

Fernando Âreas · +55-027-996087012 · fernandozanela@hotmail.com

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.

Facility not reported

Brazil

Status not reported

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