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Clinical Trials/NCT02077205
NCT02077205
Unknown
N/A

Manualised Cognitive Behavioral Therapy of Anxiety Disorders in Children and Adolescents in Routine Care Setting

Ruhr University of Bochum1 site in 1 country200 target enrollmentJanuary 2012

Overview

Phase
N/A
Intervention
Not specified
Conditions
Anxiety Disorders
Sponsor
Ruhr University of Bochum
Enrollment
200
Locations
1
Primary Endpoint
Interference rating as assessed by the "Beurteilung der Beeinträchtigung/ Einschränkung des Patienten" (BEE)
Last Updated
12 years ago

Overview

Brief 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.

Registry
clinicaltrials.gov
Start Date
January 2012
End Date
December 2015
Last Updated
12 years ago
Study Type
Interventional
Study Design
Single Group
Sex
All

Investigators

Sponsor
Ruhr University of Bochum
Responsible Party
Principal Investigator
Principal Investigator

Prof. Dr. Silvia Schneider

Prof. Dr.

Ruhr University of Bochum

Eligibility Criteria

Inclusion Criteria

  • Children and adolescents aged 4-18 years
  • Primary diagnosis of an anxiety disorder:
  • Generalized Anxiety Disorder
  • Social Phobia
  • Separation Anxiety Disorder
  • Panic Disorder +/- Agoraphobia
  • Specific Phobia

Exclusion Criteria

  • Other primary diagnoses
  • Significant intellectual impairment

Outcomes

Primary Outcomes

Interference rating as assessed by the "Beurteilung der Beeinträchtigung/ Einschränkung des Patienten" (BEE)

Time Frame: 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)

The German questionnaire "Beurteilung der Beeinträchtigung/ Einschränkung des Patienten" (BEE) assesses the degree of interference.

Severity rating of diagnosis (according to the Kinder-DIPS)

Time Frame: 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)

Spence Children's Anxiety Scale (SCAS)

Time Frame: 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)

Clinical Global Improvement Impression (CGI-I)

Time Frame: 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)

Secondary Outcomes

  • 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))
  • 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))

Study Sites (1)

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