Expired Study
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Baltimore, Maryland 21205


Purpose:

This study will evaluate the effectiveness of a short-term family-based program for preventing anxiety disorders in at-risk children.


Study summary:

Anxiety disorders are serious conditions that can negatively impact a person's overall functioning. This study will enroll mothers with anxiety disorders and their children to determine whether a brief family-based intervention will reduce childhood anxiety better than standard care. Participants will be randomly assigned to either the family-based prevention program or to evaluation only for 8 weeks. Participants in the prevention program will have weekly sessions with a therapist and will learn skills to help reduce anxiety. Self- and parent-reports, diagnostic interviews, a computerized memory task, and a videotaped parent-child interaction task will be used to assess participants. Assessments will be conducted at study start and one week after intervention completion (Week 9). Follow-up visits will be conducted at 6 and 12 months after intervention completion.


Criteria:

Inclusion Criteria: - Mothers with a current, primary anxiety disorder - 7-12 year old children without an anxiety disorder Exclusion Criteria: - Mothers that do not have a current, primary anxiety disorder - 7-12 year old children with an anxiety disorder - 7-12 year old children that are currently receiving treatment for anxiety that could interfere with the study


NCT ID:

NCT00078728


Primary Contact:

Principal Investigator
Golda S. Ginsburg, PhD
Johns Hopkins University


Backup Contact:

N/A


Location Contact:

Baltimore, Maryland 21205
United States



There is no listed contact information for this specific location.

Site Status: N/A


Data Source: ClinicalTrials.gov

Date Processed: June 25, 2018

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