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Transcranial Direct Current Stimulation Aided Rehabilitation of Gait in Subacute Stroke

Status
Terminated
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01927458
Enrollment
6
Registered
2013-08-22
Start date
2013-03-31
Completion date
2015-12-31
Last updated
2017-02-07

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

Conditions

Neurorehabilitation, Stroke

Brief summary

The purpose of this study is to determine if transcranial direct current stimulation (tDCS)applied over the lower extremity motor cortex in conjunction with treadmill training is effective for improving gait in patients with subacute stroke and to evaluate the effect and predictive value of a single session of anodal tDCS.

Interventions

DEVICETranscranial Direct Current Stimulation

A direct current runs between two electrode positions and affects the excitability of the underlying brain tissue

Sponsors

University of Aarhus
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
OTHER
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Age ≥ 18 years * Onset of stroke less than 14 days * First ischemic stroke causing lower limb weakness (MRC score ≤4 in knee extensors) and gait impairment

Exclusion criteria

* Contraindications to MRI or TMS * Other neurological disorders * Significant somatic or psychiatric disorders * History of seizures * Language or cognitive disorders prohibiting participation

Design outcomes

Primary

MeasureTime frame
Maximal gait speed using the 10-m walking testBaseline and follow up immediately following the 4 weeks intervention

Secondary

MeasureTime frameDescription
Changes in cortical excitability measuresBaselineWe will measure cortical excitability using single pulse transcranial magnetic stimulation (TMS) before and after 1st stimulation session. We will compare the measurements from before stimulation to after stimulation.
Dynamometry: the maximal isometric force of muscles will be assessed by Biodex System 3 PRO dynamometerBaseline and immediately following the 4 weeks intervention

Countries

Denmark

Outcome results

None listed

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