Computerized Psychoeducation for Anxiety Sensitivity

Status

Completed

Phases

Study type

Interventional

Source

ClinicalTrials.gov

Registry ID

NCT02874417

Enrollment

Registered

2016-08-22

Start date

2013-09-30

Completion date

2014-11-30

Last updated

2016-08-22

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Anxiety Sensitivity

Brief 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.

Interventions

BEHAVIORALCAST psychoeducation

BEHAVIORALPHET

Study design

Allocation

RANDOMIZED

Intervention model

PARALLEL

Primary purpose

PREVENTION

Masking

SINGLE (Subject)

Eligibility

Sex/Gender

MALE

Age

18 Years to 65 Years

Healthy volunteers

Inclusion criteria

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

Exclusion criteria

* History of epilepsy or seizures

Design outcomes

Primary

Measure	Time frame	Description
Anxiety Sensitivity Index-3	10 minutes post intervention	Measure of anxiety sensitivity

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026