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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04865562
Other study ID # 2015-02-0011
Secondary ID
Status Completed
Phase Phase 4
First received
Last updated
Start date March 1, 2015
Est. completion date September 1, 2016

Study information

Verified date April 2021
Source University of Texas at Austin
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

An investigation of the neuropsychological processes underlying ethical decision making.


Description:

This study will investigate the influence of reward sensitivity on cheating behavior via experimental manipulation of reward sensitivity using testosterone.


Recruitment information / eligibility

Status Completed
Enrollment 30
Est. completion date September 1, 2016
Est. primary completion date May 1, 2016
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Male
Age group 18 Years to 25 Years
Eligibility Inclusion Criteria: - males between 18 and 25 Exclusion Criteria: - recruitment will be limited to male participants between 18 and 25 years who have no current conditions that would preclude the use of testosterone. Specific exclusion criteria are: - women of all ages - males younger than 18 years and older than 25 years - self-report discomfort with ingestion of testosterone for the purpose of this study - body mass index lower than 18 or higher than 27 - prior diagnosis of major depression, posttraumatic stress disorder, phobia, anxiety disorder, or other psychiatric conditions - first-degree relatives diagnosed with a psychiatric disorder - presence of a medical condition that would preclude the use of testosterone - use of medications that would preclude the use of testosterone - consumption of more than 5 cigarettes a day - current use of testosterone enhancing products, such as gels, creams, and injections

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
testosterone propionate
1mg/0.1mL solution, to be administered intranasally
0.5% cholorbutanol, saline
125 mg 0.5% cholorbutanol, 50mg saline

Locations

Country Name City State
United States Robert Josephs Austin Texas

Sponsors (1)

Lead Sponsor Collaborator
University of Texas at Austin

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Measure of ethical behavior - Cheating rate defined as the Average number of 'heads' coin flips participants claim to have obtained drug administration following by behavioral outcome. Specifically, participants will have the opportunity to predict the outcome of a series of coin flips. To obtain a measure of ethical behavior, participants will have the opportunity to cheat by over-reporting their prediction accuracy. 90 minutes
See also
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