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Transcranial Direct Current Stimulation Aided Rehabilitation of Gait in Subacute Stroke

Not Applicable
Terminated
Conditions
Stroke
Neurorehabilitation
Interventions
Device: Transcranial Direct Current Stimulation
Registration Number
NCT01927458
Lead Sponsor
University of Aarhus
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.

Detailed Description

Not available

Recruitment & Eligibility

Status
TERMINATED
Sex
All
Target Recruitment
6
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
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Exclusion Criteria
  • Contraindications to MRI or TMS
  • Other neurological disorders
  • Significant somatic or psychiatric disorders
  • History of seizures
  • Language or cognitive disorders prohibiting participation
Read More

Study & Design

Study Type
INTERVENTIONAL
Study Design
SINGLE_GROUP
Arm && Interventions
GroupInterventionDescription
anodal tDCS with treadmill trainingTranscranial Direct Current StimulationEach subject will receive 4 weeks gait treadmill training at least 3 days per week in combination with anodal transcranial Direct Current Stimulation over the primary motor cortex up to 20 min
Primary Outcome Measures
NameTimeMethod
Maximal gait speed using the 10-m walking testBaseline and follow up immediately following the 4 weeks intervention
Secondary Outcome Measures
NameTimeMethod
Changes in cortical excitability measuresBaseline

We 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

Trial Locations

Locations (1)

Hammel Neurocenter

🇩🇰

Hammel, Denmark

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