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

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02077205
Enrollment
200
Registered
2014-03-04
Start date
2012-01-31
Completion date
2015-12-31
Last updated
2014-03-04

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Anxiety Disorders

Keywords

Diagnostic and Statistical Manual of Mental Disorders-IV/-5: Anxiety Disorders in children

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.

Interventions

BEHAVIORALManualised Cognitive Behavioral Therapy

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

Sponsors

Ruhr University of Bochum
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
4 Years to 18 Years
Healthy volunteers
No

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

Design outcomes

Primary

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

MeasureTime frame
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)

Countries

Germany

Contacts

Primary ContactSilvia Schneider, Prof. Dr.
silvia.schneider@rub.de+49 (0)234 32 - 23168

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026