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
| Type | Name | Description |
|---|---|---|
| DEVICE | Arousal-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.