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NCT00051220 Clinical Trial

Treatment for Specific Phobias in Children

Anxiety Disorders Clinical Trial

Official title:
One-Session Treatment for Specific Phobias in Children

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT00051220
Other study ID # R01MH059308
Secondary ID R01MH059308DSIR
Status Completed
Phase Phase 1/Phase 2
First received January 7, 2003
Last updated June 6, 2013
Start date October 2001
Est. completion date September 2006

Study information
Verified date June 2013
Source Virginia Polytechnic Institute and State University
Contact n/a
Is FDA regulated No
Health authority United States: Federal Government
Study type Interventional

Clinical Trial Summary

This study will compare the effectiveness of three treatments in reducing symptoms of phobia in children and adolescents.

Description:

Children with specific phobias may experience academic, social, and personal distress, as well as interference in day-to-day activities. One-Session Treatment has been found a rapid and effective treatment for adults with phobic disorders. However, its utility in the treatment of childhood phobia has not been examined.

Participants are randomly assigned to 1 of 3 groups: a one-session treatment group, an education/support group, and a waitlist control group. The one-session treatment group is directly exposed to a phobia object or situation during a 3-hour treatment session. In the education/support group, children are given information about fear and phobias and are taught how to deal with them through workbook activities. Children who participate in the one-session treatment group or the education/support group are assessed 1 week post-treatment and again after 6 months. Participants with improved symptoms have a 1-year follow-up. Participants with phobias that persist at 6 months are encouraged to participate in alternative treatment. Waitlist control participants are assessed pre-treatment and 1 month post-treatment. Those who continue to have phobias at the 1-month assessment are randomly assigned to 1 of the 2 active treatments.

Recruitment information / eligibility
Status Completed
Enrollment 150
Est. completion date September 2006
Est. primary completion date September 2006
Accepts healthy volunteers No
Gender Both
Age group 7 Years to 16 Years
Eligibility Inclusion Criteria:

- Primary diagnosis of specific phobia disorder

Exclusion Criteria:

- Mental retardation

- Developmental disabilities

- Suicide threat

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Investigator, Outcomes Assessor), Primary Purpose: Treatment

Related Conditions & MeSH terms

Intervention

Behavioral:
• One-Session Treatment for Specific Phobias

Locations
Country Name City State
Sweden University of Stockholm Stockholm
United States VA Polytech. Institute and State University Blacksburg Virginia

Sponsors (2)
Lead Sponsor Collaborator
Virginia Polytechnic Institute and State University National Institute of Mental Health (NIMH)

Countries where clinical trial is conducted

United States,  Sweden, 

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