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Effects of tDCS on Quadriceps Strength After Stroke

a Controlled, Randomized Study Evaluating the Immediate Effect of One tDCS Session on Quadriceps Strength in Hemiparetic Patients.

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02109796
Acronym
tDCS(HE)
Enrollment
14
Registered
2014-04-10
Start date
2015-02-19
Completion date
2017-04-30
Last updated
2017-11-14

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

Conditions

Stroke

Keywords

tDCS, Stroke, Force, Spasticity, Gait, EMG, Isokinetic

Brief summary

Previous studies show that one session of tDCS allow to improve muscle strength in hemiparetic patients in anodal condition. We test a new electrods configuration : a anodale stimulation opposite to the cortical representation area of the injured hemisphere and a simultaneous stimulation opposite to the homonyme the cortical representation area of the healthy hemisphere. This approach seems to be the best relevant electrods configuration in order to restore the inter-hemispheric balance. We hypothesis that one session of tDCS with this electrods configuration allow to improve paretic quadriceps strength in hemiparetic patients after stroke.

Interventions

DEVICEtranscranial Direct current stimulation

Sponsors

Fondation Garches
CollaboratorOTHER
Centre d'Investigation Clinique et Technologique 805
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
TREATMENT
Masking
SINGLE (Subject)

Eligibility

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

Inclusion criteria

* written consent * hemiparetic patient after stroke in chronic phase (\> 6 months) * capacity to walk with or without technical assistance * following rehabilitation program for lower limbs

Exclusion criteria

* patient with bilateral brain lesion, cerebellar syndrom, and apraxia and/or aphasia * previous orthopedic surgery in paretic lower limb (\<6 moths) * usual tDCS contraindications * pregnant woman

Design outcomes

Primary

MeasureTime frameDescription
maximum voluntary isometric strength of knee extensors2 hoursThe maximum voluntary isometric strength of paretic knee extensors will be evaluated with a isokinetic dynamometer, which measure peak torque.

Secondary

MeasureTime frame
Resistive peak torque during passive knee flexion2h
Angle related to the resistive peak torque generation of the knee extensors2h
Amplitude of the interpolation twitch2h
EMG activation of the knee flexors and extensors during the strength evaluations (active and passive)2h
Functional evaluation of the gait performance and balance2h

Countries

France

Outcome results

None listed

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