F40
Conditions
Interventions
Group 1: As part of a multiple baseline study, people with phobias will briefly visit their anxiety situation on five consecutive dates. The adaptive AR attention task is then randomized to be complet
Sponsors
Sozialstiftung Bamberg, Klinik für Psychiatrie und Psychotherapie
Eligibility
Sex/Gender
All
Age
18 Years to No maximum
Inclusion criteria
Inclusion criteria: Presence of a phobic disorder
Exclusion criteria
Exclusion criteria: Presence of schizophrenia or delusional disorder treatment with electroconvulsive therapy during or one month prior to the study severely impaired vision
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The primary endpoint is the subjectively experienced level of anxiety (recorded at all five measurement times) on a scale from 0 to 100). | — |
Secondary
| Measure | Time frame |
|---|---|
| The following standardized anxiety questionnaires will be administered before the first and after the fifth appointment: Body Sensations Questionnaire (BSQ) Anxiety Sensitivity Index (ASI-3) Agoraphobia Cognition Scale (ACS). In addition, the current depressive symptoms are to be recorded using the following self rating and externalratimg scales: Beck Depression Inventory II (BDI-II) Montgomery-Åsberg Depression Rating Scale (MADRS) | — |
Countries
Germany
Contacts
Public ContactWolfgang Trapp
Sozialstiftung Bamberg, Klinik für Psychiatrie und Psychotherapie
Outcome results
None listed