drugset / Trial / NCT06269146

Pramipexole to Enhance Social Connections

NCT06269146

RandomizedParallel-groupQuadruple-blindTreatment

Summary

This study seeks to understand if the medication pramipexole improves social connectedness and functioning in adults (ages 18-50) who experience anxiety or depression. The study plans to enroll 108 participants total across two sites (University of California San Diego and New York State Psychiatric Institute). Pramipexole will be given in a 6-week randomized, double-blind, placebo-controlled trial. Social reward processing will be assessed using measures of brain function (fMRI), behavior, and self-report at baseline and week 6. Knowledge gained from this study will help determine the therapeutic potential of targeting the dopamine system to remediate social disconnection as an anxiety and depression intervention.

Timeline

Start
2024-05-13
Primary completion
2026-03
Completion
2026-03

Drugs

EvaluationDrugModalityDoseRoute
Comparator Pramipexole Unknown 1 mg Oral
Comparator Pramipexole Unknown 2.5 mg Oral