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Family-Based Prevention Program for Childhood Anxiety - Article


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Clinical Trial: Family-Based Prevention Program for Childhood Anxiety

This study is currently recruiting patients.

Sponsored by: National Institute of Mental Health (NIMH)
Information provided by: National Institute of Mental Health (NIMH)

Purpose

The purpose of this study is to evaluate the effectiveness of a short-term family-based prevention program for preventing anxiety disorders in at-risk children.

Condition Treatment or Intervention
Anxiety Disorders
 Behavior: Family-Based Anxiety Prevention Program

MedlinePlus related topics:  Anxiety

Study Type: Interventional
Study Design: Prevention, Randomized, Open Label, Placebo Control, Parallel Assignment, Efficacy Study

Official Title: Family-Based Prevention for Childhood Anxiety

Further Study Details: 

Expected Total Enrollment:  40

Study start: September 2003;  Expected completion: December 2005

Anxiety disorder is a serious condition 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 study completion (Week 9). Follow-up visits will be conducted at 6 and 12 months after study completion.

Eligibility

Genders Eligible for Study:  Both

Criteria

Inclusion Criteria:

  • Mothers with anxiety disorder and their 7- to 12-year-old children

Location and Contact Information

Rachel L. Grover, PhD      443-287-4349    rgrover2@jhmi.edu
Elise Baldwin      410-955-1544    elise.baldwin@jhmi.edu

Maryland
      Johns Hopkins University School of Medicine, Baltimore,  Maryland,  21205,  United States; Recruiting
Rachel L. Grover, PhD  443-287-4349    rgrover2@jhmi.edu 
Elise S. Baldwin  410-955-1544    elise.baldwin@jhmi.edu 
Golda S. Ginsburg, PhD,  Principal Investigator
Rachel L. Grover, PhD,  Sub-Investigator

More Information

Study ID Numbers:  MH63427-01
Record last reviewed:  March 2005
Last Updated:  March 2, 2005
Record first received:  March 5, 2004
ClinicalTrials.gov Identifier:  NCT00078728
Health Authority: United States: Federal Government
ClinicalTrials.gov processed this record on 2005-04-08


Source: ClinicalTrials.gov
Cache Date: April 9, 2005


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Page Updated: September 6, 2005
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