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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00043537
Other study ID # R01MH053703
Secondary ID R01MH053703
Status Completed
Phase Phase 3
First received August 9, 2002
Last updated July 31, 2013
Start date April 2001
Est. completion date September 2006

Study information

Verified date July 2013
Source University of Central Florida
Contact n/a
Is FDA regulated No
Health authority United States: Federal Government
Study type Interventional

Clinical Trial Summary

This 4-year study will compare the long-term effectiveness of behavioral treatment, fluoxetine (Prozac®), and placebo for treatment of social phobia in children and adolescents.


Description:

Social phobia affects 3-5 percent of children, and prevalence rises with age. Youth with social phobia fear many activities that are part of everyday life and suffer from problems such as headaches or stomachaches, panic, avoidance, general anxiety, depression, loneliness, and a very restricted range of social relationships. Recent findings indicate a new psychosocial treatment called Social Effectiveness Therapy for Children (SET-C) is effective in treating children ages 8-11, resulting in reduced emotional distress and improved social functioning. Treatment effects have been maintained for up to 6 months. This study will examine SET-C in children ages 8-15. Because available data suggest that the drug fluoxetine is a promising treatment, SET-C will be compared to fluoxetine in this trial. Durability of treatment will be monitored over a 1-year follow-up period.


Recruitment information / eligibility

Status Completed
Enrollment 139
Est. completion date September 2006
Est. primary completion date September 2006
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Both
Age group 8 Years to 16 Years
Eligibility Inclusion Criteria:

- Diagnosis of social phobia

Exclusion Criteria:

- Pervasive developmental disorders (PDD)

- Schizophrenia

- Major Depression

- IQ of less than 80

- Medical conditions contraindicating use of fluoxetine

Study Design

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


Related Conditions & MeSH terms


Intervention

Behavioral:
Social Effectiveness Therapy for Children (SET-C)

Drug:
Fluoxetine

Pill Placebo


Locations

Country Name City State
United States Maryland Center for Anxiety Disorders University of Maryland, College Park Maryland

Sponsors (2)

Lead Sponsor Collaborator
University of Central Florida National Institute of Mental Health (NIMH)

Country where clinical trial is conducted

United States, 

References & Publications (1)

Beidel DC, Turner SM, Sallee FR, Ammerman RT, Crosby LA, Pathak S. SET-C versus fluoxetine in the treatment of childhood social phobia. J Am Acad Child Adolesc Psychiatry. 2007 Dec;46(12):1622-32. — View Citation

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