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Effect of Behavior Therapy on Responses to Social Stimuli in People With Social Phobia

fMRI of Emotional Reactivity Cognitive Regulation and CBT for Social Phobia

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00380731
Enrollment
124
Registered
2006-09-26
Start date
2006-09-30
Completion date
2011-08-31
Last updated
2011-11-30

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Social Phobia

Keywords

Social Anxiety Disorder, Magnetic Resonance Imaging, Cognitive Behavior Therapy

Brief summary

This study will evaluate the effect of cognitive behavioral therapy on the brain during emotional and behavioral responses to social stimuli in people with social phobia.

Detailed description

Social phobia, also known as social anxiety disorder, is a common, often debilitating condition. People with social phobia experience high levels of anxiety when they participate in social situations or perform in front of others. Approximately 80% of social phobia cases occur before the age of 18, and often precede other anxiety, mood, and substance abuse or dependence disorders. Physical symptoms typically accompany the intense anxiety caused by the disorder, and may include blushing, profuse sweating, trembling, nausea, and difficulty talking. Cognitive-behavioral therapy (CBT) has been shown to be an effective treatment method for most people with social phobia. Approximately 30% of people with the disorder, however, do not respond to CBT treatment. A better understanding of the neural mechanisms underlying social phobia and CBT's effect on these mechanisms will help physicians to better predict the best treatment for different patients. This study will evaluate the effect of CBT on how the brain processes emotional and behavioral responses to social stimuli in people with social phobia. Participants in this open-label study will be randomly assigned to either immediate or delayed treatment with CBT. Participants who are assigned to immediate CBT will attend 16 sessions of individual CBT immediately following baseline assessments. Participants assigned to the delayed treatment condition will begin attending CBT sessions approximately 5 months following baseline assessments. Outcomes will be assessed for all participants at baseline, immediately post-treatment, and at Months 5 and 10 post-treatment. An fMRI scan will be used to measure neural responses to social stimuli, and various questionnaires and scales will be used to assess anxiety symptom severity. Participants in the delayed treatment group will be assessed on one additional occasion before they begin treatment after the 5-month waiting period.

Interventions

CBT includes 16 weekly 60-minute individual CBT sessions for social anxiety disorder.

Sponsors

National Institute of Mental Health (NIMH)
CollaboratorNIH
Stanford University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
21 Years to 55 Years
Healthy volunteers
No

Inclusion criteria

* Meets DSM-IV criteria for generalized social phobia * English-speaking * Eligible to participate in fMRI scanning * Willing to use an effective form of contraception throughout the study

Exclusion criteria

* Currently undergoing any psychotherapy or pharmacotherapy (e.g, selective serotonin reuptake inhibitors, benzodiazepines, beta-blockers, anti-psychotics, blood thinners, thyroid hormone influencing agents, diabetic medications, or anticonvulsants) * History of neurological or cardiovascular disorders, brain surgery, electroconvulsive or radiation treatment, brain hemorrhage or tumor, stroke, seizures or epilepsy, diabetes, hypo- or hyperthyroidism, or head trauma with loss of consciousness for more than 5 minutes * Smokes cigarettes daily * History of or current diagnosis of schizophrenia, schizoaffective disorder, organic mental disorder, bipolar disorder, or antisocial, schizotypal, or schizoid personality disorders * Suicidal thoughts * Clinically significant and/or unstable medical disease * Pregnant or breastfeeding * Alcohol or substance abuse or dependence within the 12 months prior to study entry * History of or current seizure disorder (except febrile seizure disorder during childhood)

Design outcomes

Primary

MeasureTime frame
Liebowitz Social Anxiety ScaleMeasured at Months 4, 7, 10, 13, and 16
fMRI BOLD responseMeasured at Month 4
Behavioral assessmentMeasured at Months 4 and 16

Secondary

MeasureTime frame
Clinical Global Impression Improvement ScaleMeasured at Months 4 and 16
Quality of Life InventoryMeasured at Months 4, 10, and 16
Social Interaction Anxiety ScaleMeasured at Months 4, 10, and 16
Sheehan Disability ScaleMeasured at Months 4, 10, and 16

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 22, 2026