ClinicalTrials.Veeva

Menu

The Effect of Timing of Transcranial Direct Current Stimulation (tDCS) for Enhancing Learning During Cognitive Training

T

The University of New South Wales

Status

Completed

Conditions

Effects on Learning

Treatments

Device: Transcranial direct current stimulation (tDCS)

Study type

Interventional

Funder types

Other

Identifiers

NCT01339585
HREC 11064

Details and patient eligibility

About

This project will investigate a novel strategy for enhancing cognitive training (CT). Specifically, the investigators aim to combine a non-invasive form of brain stimulation (tDCS) with CT. This study will examine the optimal time interval - whether tDCS should be administered either before or during CT.

Enrollment

20 patients

Sex

All

Ages

18 to 40 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Participants will be healthy right-handed subjects aged 18 to 40 years.

Exclusion criteria

  • Concurrent medication likely to affect mental performance,
  • Current history of drug or alcohol abuse or dependence,
  • Any psychiatric or neurological disorder,
  • Recent head injury, or history of seizure or stroke.

Trial design

Primary purpose

Basic Science

Allocation

Randomized

Interventional model

Crossover Assignment

Masking

Single Blind

20 participants in 2 patient groups

Timing of tDCS
Experimental group
Treatment:
Device: Transcranial direct current stimulation (tDCS)
Alternative timing of tDCS
Experimental group
Treatment:
Device: Transcranial direct current stimulation (tDCS)

Trial contacts and locations

1

Loading...

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2026 Veeva Systems