Cognitive Biases Modification Treatment for Social Anxiety (CBMSP)
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Purpose
Adults with Social Phobia will be randomly assigned to either an attention bias modification treatment, interpretation bias modification treatment, both, or a placebo control condition not designed to change cognitive bias patterns.
Outcome measures will be social anxiety symptoms and severity as measured by gold standard questionnaires as well as diagnosis of social phobia disorder and symptom counts derived from structured clinical interviews based on DSM-IV criteria.
The investigators expect to find significant reduction in social anxiety symptoms in the Treatment groups relative to the placebo control group. The investigators want to find out the relative efficacy of attention and interpretation oriented treatments and the combination of the two.
| Condition | Intervention | Phase |
|---|---|---|
|
Social Phobia |
Behavioral: Attention Bias Modification Treatment (ABMT) Behavioral: Interpretation Bias Modification (IBM) Behavioral: Control Condition Behavioral: Attention and Interpretive biases modification (CBM) |
Phase 2 |
| Study Type: | Interventional |
| Study Design: | Allocation: Randomized Intervention Model: Factorial Assignment Masking: Double Blind (Subject, Investigator, Outcomes Assessor) Primary Purpose: Basic Science |
| Official Title: | Cognitive Biases Modification Treatment for Social Anxiety |
- Social Anxiety Scale (LSAS) - diagnostic interview [ Time Frame: Expected time frame of 6 weeks per participant. Participants will be assessed before and after the administration of the training/control protocols ] [ Designated as safety issue: No ]LSAS is a 24-items clinician-administered scale developed for the assessment of fear and avoidance associated with social. The LSAS assesses a wide range of both social interaction and performance/observation situations, which are rated for degree of fear/anxiety and frequency of avoidance.
- The Mini International Neuropsychiatric Interview (MINI). [ Time Frame: expected time frame of 6 weeks per participant. Participants will be assessed before and after the administration of the training/control protocols ] [ Designated as safety issue: No ]The Mini International Neuropsychiatric Interview (MINI) is a short diagnostic structured interview (DSI) developed to explore 17 disorders according to Diagnostic and Statistical Manual diagnostic criteria (DSM)
| Estimated Enrollment: | 120 |
| Study Start Date: | January 2012 |
| Estimated Study Completion Date: | February 2015 |
| Estimated Primary Completion Date: | February 2014 (Final data collection date for primary outcome measure) |
| Arms | Assigned Interventions |
|---|---|
|
Placebo Comparator: Placebo
repeated trials of a dot-probe task and repeated trials of an interpretation task, both not intended to change threat-related biases patterns.
|
Behavioral: Control Condition
Attention and interpretation training using a computerized tasks not intended to alter threat-related biases patterns.
|
|
Experimental: Attention Bias Modification (ABM)
Attention training via repeated trials of a dot-probe task intended to direct attention away from threat stimuli.
|
Behavioral: Attention Bias Modification Treatment (ABMT)
Attention training using a computerized spatial attention task (dot-probe) modified to alter threat-related attention patterns.
|
|
Experimental: Interpretation Bias Modification (IBM)
Interpretation training intended to facilitating a more benign interpretation bias
|
Behavioral: Interpretation Bias Modification (IBM)
Interpretive Bias Modification Treatment (IBMT) using a computerized task modified to facilitate a more benign interpretation bias.
|
|
Experimental: Attention and interpretation biases modification
Attention and interpretation training intended to direct cognitive biases away from threat stimulus.
|
Behavioral: Attention and Interpretive biases modification (CBM)
Attention and interpretation training via computerized tasks intended to direct attention away from threat stimuli and to facilitate a more benign interpretation bias.
|
Eligibility| Ages Eligible for Study: | 18 Years to 65 Years |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | No |
Inclusion Criteria:
People suffering from social anxiety
Exclusion Criteria:
Pharmacological or Psychological treatment
Contacts and Locations| Contact: Yair Bar-Haim, PhD | 972-3-6405465 | yair1@post.tau.ac.il |
| Contact: Reut Naim, M.A. | 972-54-6570555 | reutnaim@gmail.com |
| Israel | |
| Tel-Aviv University | Recruiting |
| Tel-Aviv, Israel | |
| Contact: Yair Bar-Haim, Professor 972-3-6405465 yair1@post.tau.ac.il | |
| Contact: Reut Naim, M.A. 972-54-6570555 reutnaim@gmail.com | |
| Principal Investigator: Yair Bar- Haim, Professor | |
More Information
No publications provided
| Responsible Party: | Yair Bar-Haim, Study Principal Investigator, Tel Aviv University |
| ClinicalTrials.gov Identifier: | NCT01503151 History of Changes |
| Other Study ID Numbers: | CBM_SP_2012 |
| Study First Received: | December 29, 2011 |
| Last Updated: | January 12, 2012 |
| Health Authority: | Israel: Tel Aviv University Ethics Commission |
Keywords provided by Tel Aviv University:
|
attention bias modification treatment interpretive bias modification cognitive bias modification attention training social anxiety |
Additional relevant MeSH terms:
|
Anxiety Disorders Phobic Disorders Mental Disorders |
ClinicalTrials.gov processed this record on May 21, 2013