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The Effect of Acute Transcranial Bright Light on Anxiety Symptoms

Anxiety Clinical Trial

Official title:
The Effect of Acute Transcranial Bright Light on Anxiety Symptoms

Clinical Trial Summary

The purpose of this study is to determine if transcranially administered bright light has acute effect on anxiety symptoms.

Clinical Trial Description

Subjects (n=30) with anxiety symptoms will be recruited into the study. To be included into the study, subjects have to get at least seven points in BAI(Becks Anxiety Inventory). At the beginning of the study subject will be randomly assigned to 12 minutes of acute transcranial bright light or placebo exposure group. Anxiety symptoms will be measured using Spielberger State-Trait Anxiety Inventory (STAI, form Y1)self-rating questionnaire just before and 10 and 110 minutes after the experiment. ;

Study Design

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

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT01938937
Study type Interventional
Source University of Oulu
Contact
Status Completed
Phase N/A
Start date March 2012
Completion date February 2014
View Details
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