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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT04460378
Other study ID # ChariteAmb
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
Start date January 1, 2018
Est. completion date October 1, 2020

Study information

Verified date July 2020
Source Charite University, Berlin, Germany
Contact Jens Plag, Dr.
Phone +49 30 450 510 306
Email jens.plag@charite.de
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Cognitive behavioral treatment of homebound patients with severe agoraphobia.


Description:

Homebound patients with severe agoraphobia are treated with an exposure focussed cognitive behavioral therapy. The treatment begins at home. With a quick onset of guided exposure, patients get the possibility to develope the capability to reach the regular Treatment Location on their own very rapidly.


Recruitment information / eligibility

Status Recruiting
Enrollment 20
Est. completion date October 1, 2020
Est. primary completion date July 1, 2020
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria:

- agoraphobia with/without Panic disorder

Exclusion Criteria:

- psychotic disorders

- bipolar disorders

- acute substance dependency

Study Design


Related Conditions & MeSH terms


Intervention

Behavioral:
cognitive behavioral therapy
cognitive behavioral therapy with Focus on guided exposure

Locations

Country Name City State
Germany Charité - Universitätsmedizin Berlin Berlin

Sponsors (3)

Lead Sponsor Collaborator
Charite University, Berlin, Germany Humboldt-Universität zu Berlin, Stiftung Deutsche Klassenlotterie Berlin

Country where clinical trial is conducted

Germany, 

Outcome

Type Measure Description Time frame Safety issue
Primary MI Mobility Inventory Change from baseline to 4th psychotherapy session (+42 days) and change from baseline to the 9th psychotherapy session (+60 days) and change from baseline to follow up (+98 days)
Secondary AKF Angst-Kontroll-Fragebogen (anxiety control) Change from baseline to 4th psychotherapy session (+42 days) and change from baseline to the 9th psychotherapy session (+60 days) and change from baseline to follow up (+98 days)
Secondary ASI Angstsensitivität (anxiety sensitivity) Change from baseline to 4th psychotherapy session (+42 days) and change from baseline to the 9th psychotherapy session (+60 days) and change from baseline to follow up (+98 days)
Secondary NEO-FFI Persönlichkeitsfragebogen (personality inventory) Change from baseline to 4th psychotherapy session (+42 days) and change from baseline to the 9th psychotherapy session (+60 days) and change from baseline to follow up (+98 days)
Secondary PSQ 20 perceived stress questionnaire Change from baseline to 4th psychotherapy session (+42 days) and change from baseline to the 9th psychotherapy session (+60 days) and change from baseline to follow up (+98 days)
Secondary rs 13 Resilienzskala (resilience scale) Change from baseline to 4th psychotherapy session (+42 days) and change from baseline to the 9th psychotherapy session (+60 days) and change from baseline to follow up (+98 days)
Secondary SWE Selbstwirksamkeitsfragebogen (self-efficacy questionnaire) Change from baseline to 4th psychotherapy session (+42 days) and change from baseline to the 9th psychotherapy session (+60 days) and change from baseline to follow up (+98 days)
Secondary UI18 Unsicherheitsintoleranz Fragebogen (intolerance of uncertainty questionnaire) Change from baseline to 4th psychotherapy session (+42 days) and change from baseline to the 9th psychotherapy session (+60 days) and change from baseline to follow up (+98 days)
Secondary EQ-5D life quality questionnaire Change from baseline to 4th psychotherapy session (+42 days) and change from baseline to the 9th psychotherapy session (+60 days) and change from baseline to follow up (+98 days)
Secondary AAQ II Acceptance and Action questionnaire Change from baseline to 4th psychotherapy session (+42 days) and change from baseline to the 9th psychotherapy session (+60 days) and change from baseline to follow up (+98 days)
Secondary ACQ Agoraphobic cognition questionnaire Change from baseline to 4th psychotherapy session (+42 days) and change from baseline to the 9th psychotherapy session (+60 days) and change from baseline to follow up (+98 days)
Secondary BSQ Bosy Sensation Questionnaire Change from baseline to 4th psychotherapy session (+42 days) and change from baseline to the 9th psychotherapy session (+60 days) and change from baseline to follow up (+98 days)
Secondary BDI II Beck Depression inventory II Change from baseline to 4th psychotherapy session (+42 days) and change from baseline to the 9th psychotherapy session (+60 days) and change from baseline to follow up (+98 days)
Secondary alpha-amylase daily profile of salivary alpha amylase change from baseline to follow up (+98 days)
Secondary cortisol daily profile of salivary cortisol change from baseline to follow up (+98 days)
Secondary PAS Panik- und Agoraphobie-Skala (Panic and agoraphobia scale) Change from baseline to 4th psychotherapy session (+42 days) and change from baseline to the 9th psychotherapy session (+60 days) and change from baseline to follow up (+98 days)
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