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Trials / Completed

CompletedNCT02493010

Arousal Training for Social Anxiety Disorder

Arousal Detection and Training for Social Anxiety Disorder (SAD)

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
50 (actual)
Sponsor
Duke-NUS Graduate Medical School · Academic / Other
Sex
All
Age
21 Years – 35 Years
Healthy volunteers
Accepted

Summary

The primary objective of the study is to examine the safety, usability and preliminary efficacy of a novel arousal-based biofeedback system in alleviating social anxiety. The investigators hypothesize that after 4 weeks of hour-long interventions, participants will show reductions pre- and post-intervention in their Liebowitz Social Anxiety Scale scores.

Detailed description

The investigators plan to conduct a waitlist control trial. Intervention consists of a combination of computerized cognitive behavioral therapy and arousal-based Virtual Reality Exposure Therapy. During the latter component, the physiological variables of participants, such as pulse rate and EEG, will be continuously monitored and presented as feedback to them. Participants will have to deliver speeches to videotaped audiences while striving to regulate their physiological arousal.

Conditions

Interventions

TypeNameDescription
DEVICEArousal-based biofeedback system

Timeline

Start date
2016-02-01
Primary completion
2017-07-01
Completion
2017-07-01
First posted
2015-07-09
Last updated
2017-12-19

Locations

1 site across 1 country: Singapore

Source: ClinicalTrials.gov record NCT02493010. Inclusion in this directory is not an endorsement.

Arousal Training for Social Anxiety Disorder (NCT02493010) · Clinical Trials Directory