Panic Treatment on the Way: Evaluating the Efficacy of an App-Enhanced Online-Intervention for the Treatment of Panic Disorder



Matthias Berking*, Friedrich-Alexander-University Erlangen-Nuremberg, Erlangen, Germany
Laura Ebenfeld, Leuphana University Lueneburg, Lueneburg, Germany
Stefan Kleine Stegemann, Leuphana University Lüneburg, Lueneburg, Germany
David Daniel Ebert, Leuphana University Lueneburg, Lueneburg, Germany
Dirk Lehr*, Leuphana University Lueneburg, Lueneburg, Germany
Heleen Riper, Free University of Amsterdam, Amsterdam, Netherlands
Pim Cujpers, Free University of Amsterdam, Amsterdam, Netherlands


Track: Research
Presentation Topic: Mobile & Tablet Health Applications
Presentation Type: Rapid-Fire Presentation
Submission Type: Single Presentation

Building: Sheraton Maui Resort
Room: A - Wailuku
Date: 2014-11-13 02:00 PM – 02:45 PM
Last modified: 2014-09-04
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Abstract


Background: Panic disorder is one of the most prevalent anxiety disorders. Contemporary research has demonstrated the efficacy of internet-based interventions for this highly debilitating mental-health problem. However, desktop-based approaches cannot effectively support patients when working with anxiety symptoms away from home. Smartphone-based interventions, however, can be used in these situations and my thus be an effective adjunctive component of online-based interventions.

Objective: The goal of this study is to evaluate the efficacy of a newly developed online-based hybrid intervention for panic disorder. GET.ON PANIC APP combines a desktop-bound intervention with a smartphone-based app that allows patients to engage in therapeutic exercises away from home.

Methods: The efficacy of the GET.ON PANIC APP is being evaluated in a randomized controlled trial with N=90 participants meeting criteria for panic disorder according to SCID-based diagnostic interviews. Eligible participants are randomly assigned to either a GET.ON PANIC APP condition or to a waiting list condition. Primary outcome is the severity of panic disorder symptoms as assessed by standardized self-reports. Secondary outcomes include observer-based ratings of anxiety and depressive symptom severity. Assessments are schedule at pre and post treatment as well as after a 6-moths follow-up period.

Results: Research in progress. Findings will be presented at the conference.

Conclusions: Research in progress. Conclusions will be discussed when presenting the findings.




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