Computerized Psychoeducation for Anxiety Sensitivity

Anxiety Sensitivity Clinical Trial

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT02874417
• Other study ID #: Norr01
• Status: Completed
• Phase: N/A
• First received: August 8, 2016
• Last updated: August 16, 2016
• Start date: September 2013
• Est. completion date: November 2014

Study information

• Verified date: August 2016
• Source: Florida State University
• Contact: n/a
• Is FDA regulated: No
• Health authority: United States: Institutional Review Board
• Study type: Interventional

Clinical Trial Summary

This investigation examines the efficacy of a 35 minute computerized psychoeducation protocol in the reduction of elevated anxiety sensitivity cognitive concerns, a risk factor for the development and maintenance of various forms of psychopathology.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 54
• Est. completion date: November 2014
• Est. primary completion date: November 2014
• Accepts healthy volunteers: No
• Gender: Male
• Age group: 18 Years to 65 Years

Eligibility

Inclusion Criteria:

• Elevated Anxiety Sensitivity Cognitive Concerns and indicated by the anxiety sensitivity index-3

Exclusion Criteria:

• History of epilepsy or seizures

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Single Blind (Subject), Primary Purpose: Prevention

Related Conditions & MeSH terms

• Anxiety Disorders
• Anxiety Sensitivity
• Hypersensitivity

Intervention

Behavioral:
• CAST psychoeducation

• PHET

Locations

Country	Name	City	State
n/a

Sponsors (1)

Lead Sponsor	Collaborator
Florida State University

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Anxiety Sensitivity Index-3	Measure of anxiety sensitivity	10 minutes post intervention	No