View Clinical Trial (Medical Research Study)
Assessing Different Methods of Anxiety Care in Pediatric Settings - NCT00769925-92123(Clinical Trial 246168)
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| City: |
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San Diego |
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State:
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CA |
| Zip Code: |
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92123 |
| Conditions: |
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Anxiety Disorders |
| Purpose: |
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This study will compare the effectiveness of delivering cognitive behavioral therapy for
children with anxiety disorders through in-person contact versus through workbooks and
telephone communication.
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| Study summary: |
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Approximately 13% of adolescents aged 9 to 17 suffer from an anxiety disorder, which can
cause disruptive fear, worry, or uneasiness that impairs their normal functioning. These
anxiety disorders can include generalized anxiety disorder (GAD), phobias, panic disorder,
and obsessive-compulsive disorder (OCD), and they often co-occur with a second anxiety
disorder or another mental or behavioral disorder, like depression. Research on
interventions such as cognitive behavioral therapy (CBT) indicates that these interventions
are helpful to children who suffer from anxiety disorders, but are not always used. This
study will examine the feasibility of implementing CBT for children between the ages of 8
and 13 in two different forms: through in-person contact at the pediatric primary care
setting and through telephone-based contact.
Participants in this study will be randomly assigned to receive either cognitive behavioral
therapy in primary care (CBT-PC) or therapist-assisted bibliotherapy in primary care
(TAB-PC). In CBT-PC, participants will have therapy administered by a child anxiety
specialist, and the parents of participants will learn how to support the new skills their
children learn in therapy. In TAB-PC, parents will receive educational workbooks and ongoing
support over the phone from a child anxiety specialist to learn how to use CBT skills to
manage their children's fears and worries. Participation in this study will last 3 to 4
months, with therapy visits occuring once a week at the beginning and tapering to once every
other week at the end of treatment. At pre-treatment, mid-treatment, post-treatment, and a
3-month follow-up, participants will undergo structured clinical interviews to assess their
anxiety levels and the severity of their conditions. |
| Criteria: |
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Inclusion Criteria:
- Meets DSM-IV criteria for one of the following disorders: separation anxiety
disorder, social phobia, generalized anxiety disorder, specific phobia, or
obsessive-compulsive disorder
- Takes a medication and has maintained a stable dose for 3 months before baseline
assessment
- Pediatric medical care is provided through one of the participating primary care
clinics
- Parent and child are fluent in English
Exclusion Criteria:
- Presence of a life threatening condition or a medical illness that would make
participation unsafe
- Diagnosed with bipolar disorder I, mental retardation, or autism or has psychotic
symptoms
- Acutely suicidal or homicidal or exhibiting dangerous behavior
- Parents do not consent for diagnosis and progress to be shared with their child's
primary care physician |
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| Study is available at: |
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University of California San Diego San Diego, CA 92123 United States
Primary Contact: Amy Drahota, PhD Email: adrahota@ucsd.edu Phone: 858-966-7703 |
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If you are interested in this clinical trial please use the contact information above. If you would like to get additional information about this clinical trial please visit ClinicalTrials.gov.
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| Data Source: |
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ClinicalTrials.gov |
| Date Processed: |
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March 22, 2011 |
Modifications to
this listing: |
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Only selected fields are shown, please use the link
above to view all information about this clinical trial. |
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