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临床试验/NCT00184106
NCT00184106已完成4 期

A Randomised, Triple Blind, Placebo-controlled Trial Comparing the Effects of Cognitive Therapy, Paroxetine and Both Cognitive Therapy and Paroxetine in the Treatment of Patients With Primary Social Phobia

Norwegian University of Science and Technology1 个研究点 分布在 1 个国家目标入组 86 人开始时间: 2004年10月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
4 期
状态
已完成
入组人数
86
试验地点
1
主要终点
The proportion responders as measured by FAIR OF NEGATIVE EVALUATION and SPAI at 12 and 24 week.

研究概览

简要总结

We aim to (1) evaluate the effectiveness of cognitive therapy and paroxetine and their combination, (2) investigate the patterns of change and the mechanisms of action involved during treatment by using psycho-physiological assessments in order to delineate some of the cognitive, behavioural and physiological mechanisms in the patients' response to CT, to paroxetine and placebo.One hundred patients with a primary diagnosis of social phobia will be selected and randomised into four treatment conditions. The first group (N=25) will be treated with CT alone, the second group (N=25) with CT plus paroxetine, the third group (N=25) with paroxetine and clinical management (TAU), the fourth group will receive placebo and clinical management (N=25). All patients will have 12 weeks of treatment in the acute phase, which includes 12 sessions of individual treatment for the two first groups. The 2nd and 3rd groups will in addition have 12 weeks of drug treatment in the maintenance phase. The 4th group will have placebo for 24 weeks and clinical management. The patients will be assessed at pre-treatment, at 12 weeks and at the end of treatment of the acute phase (12 weeks) and by the end of maintenance phase (24 weeks). Follow-up will be at 6 and 12 months.

Measures are based on all three main sources; self-report inventories, clinical assessments by independent raters and psycho-physiological assessments.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Factorial
主要目的
Treatment
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

  • Signed written informed consent obtained prior to entry in the study.
  • Diagnosed with primary social phobia, generalized or specific (DSM-IV, APA, 1994).
  • Symptoms present at least one year.
  • Age between 18-65 years.

排除标准

  • Known somatic diseases.
  • Pregnant (*) or lactating women.
  • Acute suicidal symptoms
  • Major depressive disorder
  • Generalized Anxiety Disorder or PTSD
  • Cluster A or cluster B personality disorder
  • Substance abuse or dependence
  • Body dysmorphic disorder.
  • Not willing to accept random allocation.
  • Patients who take some form of SSRI medications currently or during the last 6 months
  • Patients not willing to withdraw psychotropic medication for a period of 4 weeks prior to entry to the trial or are taking herbal remedies that may be hazardous or inflict treatment response.

研究组 & 干预措施

Cognitive Therapy

Active Comparator

Cognitive Therapy

干预措施: Seroxat, Cognitive therapy, Seroxat+ cognitive therapy (Drug)

Seroxat and SE

Active Comparator

SSRI with Self exposure

干预措施: Seroxat, Cognitive therapy, Seroxat+ cognitive therapy (Drug)

Seroxat and Cognitive Therapy

Active Comparator

Combination of Seroxat and Cognitive Therapy

干预措施: Seroxat, Cognitive therapy, Seroxat+ cognitive therapy (Drug)

Pill-Placebo

Placebo Comparator

Pill Placebo

干预措施: Seroxat, Cognitive therapy, Seroxat+ cognitive therapy (Drug)

结局指标

主要结局

The proportion responders as measured by FAIR OF NEGATIVE EVALUATION and SPAI at 12 and 24 week.

时间窗: December 2010

A patient is classified as responder if the decrease on FNE is equivalent with or above 40%.

时间窗: December 2010

次要结局

  • Relapse rate during 6 and 12 months of follow up.(December 2010)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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