Comparison of effects of neurofeedback and transcranial electrical stimulation on motor learning in healthy subjects

Comparison of short and long term effects of neurofeedback and transcranial electrical stimulation on the visuomotor skill learning in healthy subjects

Status

Recruiting

Phases

Unknown

Study type

Interventional

Source

IRCT

Registry ID

IRCT20221016056187N1

Enrollment

100

Registered

2022-11-19

Start date

2022-12-22

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

The effect of transcranial direct current stimulation and neurofeedback on motor learning.

Interventions

Intervention 1: Intervention group 1: transcranial direct current stimulation: To apply tdcs , the transcranial direct current device model neurostim 2 of Medina Tab Gostar Company is used. Before the

Eligibility

Sex/Gender

All

Age

18 Years to 40 Years

Inclusion criteria

Inclusion criteria: healthy (both genders) 18-40 years old

Exclusion criteria

Exclusion criteria: having a history of neurological diseases such as epilepsy and convulsions, concussion and migraine having an orthopedic or neurological or rheumatological injury that limits the upper limbs functions Cognitive and memory disorders (24 = (Mini-Mental State Exam Uncorrected vision problems Taking drugs affecting the central nervous system The presence of mental illnesses such as anxiety and depression that are associated with drug use Intense physical activity 2 hours before the test A history of doing activities that require a lot of dexterity in the hands, such as playing the piano pregnancy sleep disorders Intracranial implants or cardiac pacemakers

Design outcomes

Primary

Measure	Time frame
Normalized reaction time. Timepoint: Before intervention/after training/35 minutes after training/48 hours after training. Method of measurement: Serial Reaction Time Task software.;The number of normalized errors. Timepoint: Before intervention/after training/35 minutes after training/48 hours after training. Method of measurement: Serial Reaction Time Task software.	—

Secondary

Measure	Time frame
Hand fatigue. Timepoint: Beginning of the first session/End of the first session. Method of measurement: Visual Analogue Scale (VAS).;Level of mental fatigue. Timepoint: Beginning of the first session/End of the first session. Method of measurement: Visual Analogue Scale (VAS).	—

Countries

Iran (Islamic Republic of)

Contacts

Public ContactSara Rezaei eshkalak

Tehran University of Medical Sciences

srh.rezaei@gmail.com+98 21 7753 5132

Outcome results

None listed

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