N/A N=40 Randomized Prevention

Family-Based Prevention Program for Childhood Anxiety

Anxiety Disorders

Bottom Line

View on ClinicalTrials.gov: NCT00078728 ↗

Enrolled (actual)

Serious AEs

0.0%

Results posted

Dec 2013

Primary outcome: Primary: Number of Children With Child Anxiety Diagnosis — 20; 20 participants

Study Design & Population

Study type: Interventional
Phase: N/A
Interventions: Family-Based Anxiety Prevention Program (Behavioral); Evaluation only (Behavioral)
Age: Pediatric, Adult, Older Adult · 7+ yrs
Sex: All
Sponsor: Johns Hopkins University
Primary completion: Jul 2007

Outcome Measures

Outcome	Result	p-value
PRIMARY Number of Children With Child Anxiety Diagnosis	20; 20	—
PRIMARY Child Anxiety Diagnoses	0; 6	—

Summary

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

Eligibility 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

View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT00078728). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.