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RECRUITING
NCT05007561
EARLY_PHASE1

Understanding How Opioids Affect the Experiential and Neural Signatures of Social Experiences

Sponsor: San Diego State University

View on ClinicalTrials.gov

Summary

The study is a randomized, placebo-controlled design with the opioid antagonist, oral naltrexone. Following random assignment, participants will take 50mg of naltrexone or placebo once a day for 7 days. On days 1 - 7, participants complete reports of their feelings of social connection and mood in order to assess more naturalistic feelings in response to opportunities for social connection outside of the laboratory setting. Additionally, at the end of each day, they complete a physical symptoms questionnaire. On the 7th day, participants will come to the SDSU MRI scanning facility to complete tasks designed to elicit feelings of social connection in the fMRI scanner. After the scan, feelings in response to the scanner tasks will be collected.

Key Details

Gender

All

Age Range

18 Years - 25 Years

Study Type

INTERVENTIONAL

Enrollment

210

Start Date

2021-11-16

Completion Date

2027-07

Last Updated

2025-04-11

Healthy Volunteers

Yes

Interventions

DRUG

Naltrexone Hydrochloride

oral naltrexone

DRUG

Placebo

oral sugar pill

Locations (1)

San Diego State University

San Diego, California, United States