Investigating the Effectiveness of a 2-week Novel Non-invasive Brain Stimulation Technique on Cognitive Outcomes in Healthy Adults

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age21-75
SponsorNanyang Technological University

About this trial

The goal of this randomised controlled trial is to investigate the effects of a 2-week high-frequency transcranial pulsed current stimulation (tPCS) on cognitive outcomes in older and healthy adults. The main questions it aims to answer are:

1. Would a single session of anodal tPCS over the left prefrontal cortex improve working memory, task inhibition, and task switching in healthy young and older adults, compared to anodal transcranial direct current stimulation (tDCS) and sham-tPCS? 2. Would repeated session of anodal-tPCS (2-weeks) lead to improvements in working memory, task inhibition, and task switching in healthy young and older adults, compared to tDCS and sham-tPCS? 3. Will tPCS be better tolerated among healthy adults, compared to tDCS?

Researchers will compare tPCS / tDCS / sham-tPCS to see if there are any differences in cognitive outcomes after 1 session and after repeated sessions, as well as to compare the tolerance of tPCS against tDCS and sham-tPCS.

Participants will be requested to:

* Undergo 1 of 3 of the following conditions: tDCS / tPCS / sham-tPCS * Complete three sessions of cognitive tasks testing working memory, inhibition and task switching at baseline (pre-stimulation), after day 1 of brain stimulation and after 10 sessions of brain stimulation (post- repeated stimulation) * Undergo fNIRS-EEG brain measurements concurrently with the cognitive tasks

Eligibility criteria

Qualifiers

Male and female young (21 to 30 years) and older adults (60 to 75 years)

Right-handed

Must be a native English speaker

No clinical diagnosis of neurodevelopmental, mood, neurological or neurodegenerative disorders

Disqualifiers

Currently on long-term medication for pain or migraines / headaches

Adults with metallic implants in the chest or head region

Adults with epilepsy, or known seizure or immediate family members that have had a seizure before

Had a recent head injury that resulted in a temporary loss of consciousness or of memory in the last 12 months

Trial design

Treatments tested in this trial

  • Non-Invasive Brain Stimulation (tDCS / tPCS / sham-tPCS)

Treatment groups

120 Participants
are divided into 3 treatment groups

Locations

This trial has no locations

Sponsors and collaborators

Nanyang Technological University

Lead sponsor

Ministry of Education, Singapore

Collaborator

National Institute of Education, Singapore

Collaborator