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Family-Based Prevention Program for Childhood Anxiety

NCT00078728 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 40

Last updated 2018-02-07

Study results available
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Summary

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

Conditions

  • Anxiety Disorders

Interventions

BEHAVIORAL

Family-Based Anxiety Prevention Program

Participants in the prevention program will have weekly sessions with a therapist and will learn skills to help reduce anxiety for 8 weeks. The intervention will begin immediately after randomization to the study.

BEHAVIORAL

Evaluation only

Participants will undergo evaluations without active treatment for 8 weeks.

Sponsors & Collaborators

Principal Investigators

  • Golda S. Ginsburg, PhD · Johns Hopkins University

Study Design

Allocation
RANDOMIZED
Purpose
PREVENTION
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
7 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2003-09-30
Primary Completion
2007-07-31
Completion
2007-07-31

Countries

  • United States

Study Locations

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Entities

Companies

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT00078728 on ClinicalTrials.gov