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Effect of transcranial direct current stimulation in diplegic cerebral palsy

Clinical trial of transcranial direct current stimulation effect on gait in children with diplegic spastic cerebral palsy

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20170703034879N3
Enrollment
20
Registered
2021-07-31
Start date
2021-09-23
Completion date
Unknown
Last updated
2021-08-30

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

Conditions

spastic diplegic Cerebral palsy. Spastic diplegic cerebral palsy

Interventions

Intervention 1: Intervention group: In intervention group direct electrical stimulation is performed using saline wet sponge
anode is placed on cortical motor area Cz and cathode is placed on forehead. There will be 30 seconds of ascending direct current at the beginning, thereafter 20 minutes of stable 2 mA current and a
anode is placed on cortical motor area Cz and cathode is placed on forehead. There will be 30 seconds of ascending direct current at the beginning, in the next 20 minutes no current is employed. There

Sponsors

Tehran University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
5 Years to 12 Years

Inclusion criteria

Inclusion criteria: Diplegic spastic cerebral palsy Gross Motor Function Classification System (GMFCS) less than 4, i.e. can walk independently or with walking aid age between 5 and 12 years

Exclusion criteria

Exclusion criteria: patient or parents do not consent history of surgery in previous 12 months uncontrolled epilepsy metallic foreign body in brain orthopedic problem needing urgent surgery cognitive problem troubling cooperation

Design outcomes

Primary

MeasureTime frame
Velocity of gait. Timepoint: gait velocity will be measured 1 week after the completion of first and second course (after crossover) of tDCS. Method of measurement: Measured during gait analysis by velocity sensors.

Secondary

MeasureTime frame
Cadence. Timepoint: cadence will be measured 1 week after the completion of first and second course (after crossover) of tDCS. Method of measurement: Measured during gait analysis by velocity and time sensors.;PEDI : Pediatric evaluation of disability inventory. Timepoint: PEDI will be filled 1 week after the completion of first and second course (after crossover) of tDCS. Method of measurement: The investigator will fill the inventory.;6MWT: six minute walk test. Timepoint: 6MWT be measured 1 week after the completion of first and second course (after crossover) of tDCS. Method of measurement: The distance walked in 6 minutes will be measured by the investigator.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr Siamak Abdi

Tehran University of Medical Sciences

Siamak.Abdi@yahoo.com+98 21 8490 2224

Outcome results

None listed

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