Evaluation of a gamified augmented reality app as part of a multiple baseline study in people with phobias

Not Applicable

Recruiting

• Conditions: F40; Phobic anxiety disorders

• Registration Number: DRKS00033470
• Lead Sponsor: Sozialstiftung Bamberg, Klinik für Psychiatrie und Psychotherapie

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Study Start: 2024-01-31
• Last Update Posted: 19 August 2024

Recruitment & Eligibility

• Status: Recruiting
• Sex: All
• Target Recruitment: 20

Inclusion Criteria

Presence of a phobic disorder

Exclusion Criteria

Presence of schizophrenia or delusional disorder
treatment with electroconvulsive therapy during or one month prior to the study
severely impaired vision

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
The primary endpoint is the subjectively experienced level of anxiety (recorded at all five measurement times) on a scale from 0 to 100).

Secondary Outcome Measures

Name	Time	Method
The following standardized anxiety questionnaires will be administered before the first and after the fifth appointment:<br>Body Sensations Questionnaire (BSQ)<br>Anxiety Sensitivity Index (ASI-3)<br>Agoraphobia Cognition Scale (ACS).<br>In addition, the current depressive symptoms are to be recorded using the following self rating and externalratimg scales:<br>Beck Depression Inventory II (BDI-II)<br>Montgomery-Åsberg Depression Rating Scale (MADRS)