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The effect of transcranial direct current stimulation on motor learning

Comparison the effect of transcranial direct current stimulation between unihemispheric concurrent dual site and primary motor cortex on motor learning in healthy individuals

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
IRCT
Registry ID
IRCT2016071028808N2
Enrollment
48
Registered
2016-11-02
Start date
2016-04-20
Completion date
Unknown
Last updated
2018-02-22

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

Conditions

Motor learning. Care involving use of rehabilitation procedures

Interventions

Intervention 1: Unihemispheric concurrent dual site transcranial direct current stimulation(tDCS UCDS) of primary motor and dorsolateral prefrontal cortices? 1 milliampere current intensity, 0.16 mil
Rehabilitation
Unihemispheric concurrent dual site transcranial direct current stimulation(tDCS UCDS) of primary motor and dorsolateral prefrontal cortices? 1 milliampere current intensity, 0.16 milliampere/ square
Transcranial direct current stimulation of primary motor cortex (tDCSm1), 1 milliampere current intensity, 0.16 milliampere/square centimeter current density, 20 minutes time of stimulation, Three co
Transcranial direct current stimulation, Sham stimulation, 1 milliampere current intensity only for the first 30 s, Turned off current for remained 20 minutes time of stimulation, Three consecutive da

Sponsors

Vice chancellor for research, University of Social Welfare and Rehabilitation Sciences
Lead Sponsor
Investigator
Collaborator

Eligibility

Sex/Gender
All
Age
18 Years to 35 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: The healthy young participants who are 18 to 35 year old; The participants who are right handed; The participants who have no history of neurological or psychiatric diseases; The participants who have no serious memory deficits; The participants who have no skin problems on the head; The participants who have no disability in upper extremity. Exclusion criteria: Several factors that stop software; The participants who leave test for any reason; Severe fatigue.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Reaction time in each block. Timepoint: 3 consecutive days. Method of measurement: In millisecond and using Superlab5 software.

Secondary

MeasureTime frame
Number of errors in each block. Timepoint: 3 consecutive days. Method of measurement: Based on the number and using Superlab5 software.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactAilin Talimkhani

University of Social Welfare and Rehabilitation Sciences

ai.talimkhani@uswr.ac.ir; ailintalimkhani@yahoo.com+98 21 2218 0039

Outcome results

None listed

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