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Transcranial Direct Current Stimulation Acute Stroke Walking

U

University of Liege

Status

Unknown

Conditions

Acute Stroke

Treatments

Device: Anodal Transcranial Direct Current Stimulation

Study type

Interventional

Funder types

Other

Identifiers

NCT04349488
2016/287

Details and patient eligibility

About

16 acute stroke patients will be split into 2 groups. One group will receive the real treatment (anodal tDCS) and one group sham.

Subjects will receive, in addition to conventional rehabilitation, 2mA for 20 mins of their attributed tDCS, 5 times a week.

Evaluations will take place before the first stimulation period (48h post stroke), after 1, 2, 3 and 4 weeks.

The evaluations are the Four Square Step Test, the Berg Balance Scale, the Postural Assessment Scale For Stroke, the Trunk Impairment Scale, the Time Up & Go and the 10 meter walking test.

Enrollment

16 estimated patients

Sex

All

Ages

18 to 80 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • First Ever Stroke
  • Motor or sensory deficit
  • Understands and follows orders
  • Signed inform consent

Exclusion criteria

• One Yes on the medium and high risk sections of the TSST (Bornheim et al.,2019)

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Quadruple Blind

16 participants in 2 patient groups, including a placebo group

Treatment
Active Comparator group
Description:
Anode placed over the affected primary motor cortex, cathode over contralateral supra orbital area. 2 mA, 20min stimulation, 5 days a week for 4 weeks
Treatment:
Device: Anodal Transcranial Direct Current Stimulation
Placebo
Placebo Comparator group
Description:
Anode montage but current is ramped up over 15 secondes, then ramped down. 2 mA, 20min stimulation, 5 days a week for 4 weeks
Treatment:
Device: Anodal Transcranial Direct Current Stimulation

Trial contacts and locations

1

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Central trial contact

Stephen Bornheim, Msc

Data sourced from clinicaltrials.gov

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