Brief Intervention to Reduce Fear

Status Not yet recruiting

Clinical Trial Summary

The study will test the efficacy of propranolol or placebo, administered after retrieval of a previously acquired public speaking fear, in reducing fear and avoidance of public speaking.

Clinical Trial Description

Twenty subjects with Performance-Only type of Social Anxiety Disorder will be enrolled in the study. They will complete baseline assessments of fear and avoidance of public speaking. They will be randomly assigned to a single dose of propranolol 40mg or placebo, administered immediately after a fear activation procedure. Primary outcome assessment will be self-reported fear of public speaking and avoidance behavior in a behavioral avoidance task 2 weeks after the intervention. ;

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Caregiver, Investigator, Outcomes Assessor)

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT02924610
Study type	Interventional
Source	Research Foundation for Mental Hygiene, Inc.
Contact	Danielle Moskow, BA
Phone	6467748013
Email	dmoskow@nyspi.columbia.edu
Status	Not yet recruiting
Phase	Phase 4
Start date	October 2016

View Details

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