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Clinical Trial Details — Status: Active, not recruiting

Administrative data

NCT number NCT04204759
Other study ID # IRB-2019-06-072
Secondary ID
Status Active, not recruiting
Phase N/A
First received
Last updated
Start date November 3, 2019
Est. completion date December 31, 2023

Study information

Verified date October 2022
Source Nanyang Technological University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The main objective of this study is to investigate the causal relationship between prefrontal cortex activity and antisocial behavior, as well as risk factors for antisocial behavior. Specifically, this study tests the hypothesis that upregulating activity in the prefrontal cortex through a non-invasive form of brain stimulation, transcranial direct current stimulation (tDCS) will reduce antisocial and aggressive behavior. The effects of 3 days of anodal stimulation over the prefrontal cortex are assessed.


Recruitment information / eligibility

Status Active, not recruiting
Enrollment 101
Est. completion date December 31, 2023
Est. primary completion date May 1, 2022
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - Above 18 (with parental consent) or above 21 (without parental consent) - Able to understand the nature of the study and give informed consent Exclusion Criteria: - History of or active neurologic, cardiovascular, or psychiatric disease including anxiety disorders (e.g., PTSD, panic attacks, obsessive-compulsive disorder) and mood disorders (e.g., depression) - Currently consuming anti-convulsant, anti-psychotic, or sedative/hypnotic medications - Currently consuming anti-depressants - History of seizures - Metallic implants on scalp - Participated in any other non-invasive brain stimulation study in the same day - Ever had an adverse reaction to tDCS

Study Design


Related Conditions & MeSH terms


Intervention

Device:
Transcranial direct current stimulation
Non-invasive stimulation will be conducted using a tDCS device (StarStim, Neuroelectrics, Spain).
Sham transcranial direct current stimulation
The same device will be used as in the active stimulation group, but stimulation will be terminated after 30 seconds.

Locations

Country Name City State
Singapore Nanyang Technological University Singapore

Sponsors (1)

Lead Sponsor Collaborator
Nanyang Technological University

Country where clinical trial is conducted

Singapore, 

Outcome

Type Measure Description Time frame Safety issue
Primary Points in the Point Subtraction Aggression Paradigm after stimulation The number of points earned on the lab task will be assessed. Within 1 hour after the third consecutive active tDCS or sham session
Primary Antisocial behavior inclinations after stimulation This will be assessed using 5 hypothetical scenarios in which someone commits a criminal or antisocial act. Participants will respond to the likelihood that they would commit the act in the scenario according to a 10-point Likert scale. Responses are measured on a scale ranging from zero (no chance at all) to 10 (100% chance). A higher value reflects a greater intention to engage in the antisocial act. Within 1 hour after the third consecutive active tDCS or sham session
Primary Moral judgment ratings after stimulation This will be assessed using 5 hypothetical scenarios in which someone commits a criminal or antisocial act. Participants will rate the moral wrongfulness of the act in the scenario on a scale from 0 (not at all) to 10 (very). A higher score reflects a greater perception of moral wrongfulness regarding the antisocial act. Within 1 hour after the third consecutive active tDCS or sham session
Primary Delay discounting rates after stimulation Participants' responses to 5 questions indicating if they would prefer a smaller reward today or a larger reward in the specified number of days will be assessed. The delay discount rates (k) of monetary rewards will be calculated based on the responses to the 5 trials. Within 1 hour after the third consecutive active tDCS or sham session
Primary Helping behavior after stimulation This will be assessed based on the number of easy and hard puzzles participants choose to assign to another participant in the study. Within 1 hour after the third consecutive active tDCS or sham session
Primary Antisocial behavior after stimulation This will be assessed based on the participants' accurate reporting of the number of problems correctly solved in a task. Within 1 hour after the third consecutive active tDCS or sham session
Secondary Number of participants with adverse events The number of participants reporting the experience of sensations resulting from tDCS will be recorded. Within 1 hour after each of the 20-minute active tDCS or sham sessions
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