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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT02077205
Other study ID # no funding
Secondary ID
Status Recruiting
Phase N/A
First received February 4, 2014
Last updated February 28, 2014
Start date January 2012
Est. completion date December 2015

Study information

Verified date February 2014
Source Ruhr University of Bochum
Contact Silvia Schneider, Prof. Dr.
Phone +49 (0)234 32 - 23168
Email silvia.schneider@rub.de
Is FDA regulated No
Health authority Germany: Local ethics comittee of the faculty of Psychology
Study type Interventional

Clinical Trial Summary

Manualised Cognitive Behavioral Therapy for children and adolescents with anxiety disorders is evaluated in a routine care setting to evaluate the efficacy of the intervention. Children and adolescents receive manualized Cognitive Behavioral Therapy for anxiety disorder.

It is expected, that the intervention will result in less anxiety / lower scores on the primary and secondary outcome measures.


Recruitment information / eligibility

Status Recruiting
Enrollment 200
Est. completion date December 2015
Est. primary completion date June 2014
Accepts healthy volunteers No
Gender Both
Age group 4 Years to 18 Years
Eligibility Inclusion Criteria:

- Children and adolescents aged 4-18 years

- Primary diagnosis of an anxiety disorder:

1. Generalized Anxiety Disorder

2. Social Phobia

3. Separation Anxiety Disorder

4. Panic Disorder +/- Agoraphobia

5. Specific Phobia

Exclusion Criteria:

- Other primary diagnoses

- Significant intellectual impairment

Study Design

Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment


Related Conditions & MeSH terms


Intervention

Behavioral:
Manualised Cognitive Behavioral Therapy
16 Sessions of Manualised Cognitive Behavioral Therapy in a Routine Care Setting

Locations

Country Name City State
Germany Ruhr-University of Bochum, Department of Psychology, AE Klinische Kinder- und Jugendpsychologie Bochum Nordrhein-Westfalen

Sponsors (1)

Lead Sponsor Collaborator
Ruhr University of Bochum

Country where clinical trial is conducted

Germany, 

Outcome

Type Measure Description Time frame Safety issue
Primary Severity rating of diagnosis (according to the Kinder-DIPS) Changes in severity rating from pre- to post-assessment (post-assessment takes place 30 weeks after the pre-assessment on average) and to 6-month-follow-up (which takes place about 6 months after the post-assessment) No
Primary Spence Children's Anxiety Scale (SCAS) Changes on the SCAS from pre- to post-assessment (post-assessment takes place 30 weeks after the pre-assessment on average) and to 6-month-follow-up (which takes place about 6 months after the post-assessment) No
Primary Clinical Global Improvement Impression (CGI-I) Changes on the CGI-I from post-assessment (post-assessment takes place 30 weeks after the pre-assessment on average) to 6-month-follow-up (which takes place about 6 months after the post-assessment) No
Primary Interference rating as assessed by the "Beurteilung der Beeinträchtigung/ Einschränkung des Patienten" (BEE) The German questionnaire "Beurteilung der Beeinträchtigung/ Einschränkung des Patienten" (BEE) assesses the degree of interference. Changes in interference rating from pre- to post-assessment (post-assessment takes place 30 weeks after the pre-assessment on average) and to 6-month-follow-up (which takes place about 6 months after the post-assessment) No
Secondary Depression as measured by the Short Moods and Feelings Questionnaire (SMFQ) Changes in the SMFQ from pre- to post-assessment (post-assessment takes place 30 weeks after the pre-assessment on average) and to 6-month-follow-up (which takes place about 6 months after the post-assessment) No
Secondary Strengths and Difficulties Questionnaire (SDQ) Changes on the SDQ from pre- to post-assessment (post-assessment takes place 30 weeks after the pre-assessment on average) and to 6-month-follow-up (which takes place about 6 months after the post-assessment) No
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