Computerized Psychoeducation for Anxiety Sensitivity

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.

Completed

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Key information

Conditions

Anxiety Sensitivity

Age range

18 year–65 year

Sex eligibility

Male

Study type

Interventional

Phase

Not applicable

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

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

Exclusion criteria

History of epilepsy or seizures

Treatment and study plan

CAST psychoeducation

Behavioral

PHET

Behavioral

Primary outcomes

Anxiety Sensitivity Index-3

Time frame: 10 minutes post intervention

Measure of anxiety sensitivity

Sponsors and collaborators

Lead sponsor

Florida State University

Other

Registry information

Important dates

Study start: 2013
Primary completion: 2014
Study completion: 2014
First posted: Aug 22, 2016
Registry last updated: Aug 22, 2016

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Published trials that share one or more normalized conditions with this study.

Completed