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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03974282
Other study ID # HM20015724
Secondary ID UL1TR002649
Status Completed
Phase N/A
First received
Last updated
Start date June 20, 2019
Est. completion date March 16, 2020

Study information

Verified date February 2023
Source Virginia Commonwealth University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

This study is about how brain function and structure is different between two universities. Participant in this project will contribute to a better understanding of how universities affect the brain.


Description:

Some study details are purposely omitted at this time to preserve scientific integrity. Now that the study is completed, full details are included below. The true purpose of this study was to investigate the psychometric properties of the two computer tasks that participants completed. Specifically, researchers wanted to know if they would be able to accurately measure motivated empathy. To better understand this, participants were asked to rate images of people expressing pain and were told that these were either students from their university or students from a different university. This was not the case. The faces shown were random images produced for a research study. Researchers also wanted to know if they could accurately measure moral decision making and how those judgments relate to aggression. To examine this, participants were asked whether various scenarios were immoral and then asked about aggressive tendencies.


Recruitment information / eligibility

Status Completed
Enrollment 36
Est. completion date March 16, 2020
Est. primary completion date March 16, 2020
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 35 Years
Eligibility Inclusion Criteria: - Undergraduate students aged 18 - 35 years of age - No current or regular use of prescribed or illicit psychoactive drugs - Free of major health problems (e.g., diabetes, HIV, Parkinson's disease) - Free of a neurological or psychiatric disorders - No current drug abuse (e.g., recreational drug use, average alcohol intake in excess of 4 drinks per day). - Right hand dominant - Free of claustrophobia - Free of pregnancy or suspected pregnancy - Absent MRI risk factors (e.g., implanted medical device, body mass index > 35, braces) - Free of medical conditions that render individuals with overly sensitive hearing - No colorblindness Exclusion Criteria: • Not meeting the inclusion criteria listed above.

Study Design


Intervention

Behavioral:
Psychological task
Participants will complete a psychological task that evokes antisocially- and prosocially-motivated empathic responding

Locations

Country Name City State
United States Virginia Commonwealth University Richmond Virginia

Sponsors (2)

Lead Sponsor Collaborator
Virginia Commonwealth University National Center for Advancing Translational Sciences (NCATS)

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Change in Prefrontal Cortex Brain Activity Assessed by fMRI Blood-Oxygen-Level-Dependent signal change in the cognitive empathy brain network will be assessed using functional MRI Baseline to 3 hours
Primary Change in Accuracy of Empathic Pain Judgments Difference in pain judgment scores rated from 1 (low) to 4 (high) between antisocial vs prosocial empathy trials Baseline to 3 hours
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