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Investigating the effect of tDCS on stroke

Study the effect of cathodal tDCS on healthy side comparing with anodal tDCS on affected side of motor cortex on lower limb muscles spasticity in patients with stroke

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20230104057044N1
Enrollment
45
Registered
2023-01-27
Start date
2023-02-20
Completion date
Unknown
Last updated
2023-02-07

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

Conditions

stroke. Stroke, not specified as haemorrhage or infarction

Interventions

Intervention 1: Intervention group: cathodal. It includes ten sessions of routine stroke physiotherapy along with cathodal TDCS. In this study, the TDCS device (ActivaDose® II, ActivaTeK™ Inc., Gilro

Sponsors

Semnan University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
40 Years to 80 Years

Inclusion criteria

Inclusion criteria: Stroke patients with an age range of 40 to 80 years At least 6 months have passed since the stroke No history of botulism injections or other invasive treatments in the past 6 months The minimum Ashworth score is 1.

Exclusion criteria

Exclusion criteria: History of epilepsy History of cerebellar aneurysm Metal implants in the brain Widespread infection (all areas of the middle cerebral artery) Severe flaccid hemiplegia head injury Other neurological or orthopedic diseases that can affect motor function Renal or hepatic impairment Report of injection of previous painkillers Severe cognitive impairment The stroke areas involve both hemispheres

Design outcomes

Primary

MeasureTime frame
The grade of spasticity in ankle plantar flexor muscles during active and passive ankle dorsiflexion. Timepoint: Before intervention, after the tenth session of the intervention, two weeks after the last session of the intervention. Method of measurement: Modified Ashworth scale and electromyography device.;Balance. Timepoint: Before intervention, after the tenth session of the intervention, two weeks after the last session of the intervention. Method of measurement: Berg balance scale.;Quality of life. Timepoint: Before intervention, after the tenth session of the intervention, two weeks after the last session of the intervention. Method of measurement: WHOQOL-BREF.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactFatemeh Ehsani

Semnan University of Medical Sciences

fatemehehsani59@yahoo.com+98 23 3365 4180

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026