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临床试验/NCT01503151
NCT01503151已完成2 期

Cognitive Biases Modification Treatment for Social Anxiety

Tel Aviv University1 个研究点 分布在 1 个国家目标入组 95 人开始时间: 2012年1月最近更新:
适应症

试验速览

阶段
2 期
状态
已完成
入组人数
95
试验地点
1
主要终点
Social Anxiety Scale (LSAS) - diagnostic interview

研究概览

简要总结

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.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Factorial
主要目的
Basic Science
盲法
Triple (Participant, Investigator, Outcomes Assessor)

入排标准

年龄范围
18 Years 至 65 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • People suffering from social anxiety

排除标准

  • Pharmacological or Psychological treatment

结局指标

主要结局

Social Anxiety Scale (LSAS) - diagnostic interview

时间窗: Expected time frame of 6 weeks per participant. Participants will be assessed before and after the administration of the training/control protocols

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.

次要结局

  • The Mini International Neuropsychiatric Interview (MINI).(expected time frame of 6 weeks per participant. Participants will be assessed before and after the administration of the training/control protocols)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Yair Bar-Haim

Study Principal Investigator

Tel Aviv University

研究点 (1)

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