Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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SUSPENDED
NA
80 participants
INTERVENTIONAL
2021-02-15
2027-02-28
Brief Summary
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Detailed Description
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Conditions
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Study Design
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RANDOMIZED
PARALLEL
TREATMENT
TRIPLE
Study Groups
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Experimental Computer-Based Treatment
A 4-week (8-sessions) course of computer-based treatment. Participants will receive treatment twice a week for four weeks.
Computer-Based Treatment
A 4-week (8 30-minute sessions) course of computer-based treatment involving viewing pictures of faces while music may play. Participants will receive research treatment twice a week.
Comparator Computer-Based Treatment
A 4-week (8-sessions) course of computer-based treatment. Participants will receive treatment twice a week for four weeks.
Computer-Based Treatment
A 4-week (8 30-minute sessions) course of computer-based treatment involving viewing pictures of faces while music may play. Participants will receive research treatment twice a week.
Interventions
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Computer-Based Treatment
A 4-week (8 30-minute sessions) course of computer-based treatment involving viewing pictures of faces while music may play. Participants will receive research treatment twice a week.
Eligibility Criteria
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Inclusion Criteria
* Current primary diagnosis of SAD
* Score of at least 50 on the Liebowitz Social Anxiety Scale (self-rated version)
* Fluent in English
* Willing and able to give informed written consent
* Ability to participate responsibly in the protocol
* Normal or corrected-to-normal vision
Exclusion Criteria
* Current severe depression
* Suicidal ideation or behavior
* Current diagnosis of post-traumatic stress disorder, obsessive-compulsive disorder, bipolar disorder, manic episode or tic disorder
* Current or past organic mental disorder, seizure disorder, epilepsy or brain injury
* Current unstable or untreated medical illness
* Severe alcohol use disorder, severe cannabis use disorder, and any severity of other substance use disorder (except nicotine use disorders)
* Use of psychiatric medication in the past month other than a stable dose of selective serotonin reuptake inhibitors (SSRIs) for at least 3 months
* Any concurrent cognitive behavioral therapy or other psychotherapy that was initiated in the past 3 months
* Pregnancy, or plans to become pregnant during the period of the study (will be assessed by urine)
* Contraindication to MRI scanning (Paramagnetic metallic implants or devices contraindicating magnetic resonance imaging or any other non-removable paramagnetic metal in the body)
1. pacemaker
2. paramagnetic metallic prosthesis
3. surgical clips
4. shrapnel
5. necessity for constant medicinal patch
6. some tattoos
* Inability to tolerate MRI scanning procedures (i.e., severe obesity, claustrophobia)
18 Years
60 Years
ALL
No
Sponsors
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Columbia University
OTHER
Mclean Hospital
OTHER
Tel Aviv University
OTHER
National Institute of Mental Health (NIMH)
NIH
New York State Psychiatric Institute
OTHER
Responsible Party
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Franklin Schneier
Director, Anxiety Disorders Clinic
Principal Investigators
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FRANKLIN SCHNEIER, MD
Role: PRINCIPAL_INVESTIGATOR
New York State Psychiatric Institute
Locations
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1051 Riverside Drive
New York, New York, United States
Countries
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Other Identifiers
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8072
Identifier Type: -
Identifier Source: org_study_id
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