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临床试验/NCT00734370
NCT00734370已完成不适用

Virtual Reality Exposure Therapy in Agoraphobic Participants

VU University of Amsterdam1 个研究点 分布在 1 个国家目标入组 55 人开始时间: 2008年10月1日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
55
试验地点
1
主要终点
Panic Disorder Severity Scale (PDSS); Mobility Inventory for Agoraphobia (MI); Behavioural Avoidance Test (BAT)

研究概览

简要总结

Virtual Reality Exposure Therapy (VRET) is an effective treatment for anxiety disorders, particularly for specific phobias as fear of heights and fear of flying (e.g. Powers & Emmelkamp, 2008). Recent technological advances (e.g. more realistic avatars) make research into the efficacy of VRET for participants with elevated agoraphobic symptoms desirable. Therefore, the aim of the present research proposal is to investigate the comparative efficacy of:

  1. enhanced VRET making use of the latest avatar technology with
  2. exposure in vivo in agoraphobic participants
  3. wait-list control.

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
None

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

  • A full diagnosis of panic disorder with agoraphobia according to the DSM-IV
  • Between the ages of 18-65 years
  • Sufficient fluency in Dutch to complete treatment and research protocol

排除标准

  • Presence of medical condition, assessed by self-report questionnaires at the intake (i.e., pregnancy, seizure disorder, pacemaker)
  • Current use of Beta-blockers
  • Current use of tranquilizers (Benzodiazepines)
  • Unstable psychotropic medication
  • Substance dependence
  • Psychosis
  • Depression with suicidal ideation
  • Posttraumatic Stress Disorder
  • Dementia or other severe cognitive impairment
  • Bipolar Disorder
  • Borderline Personality Disorder
  • Anti-social Personality Disorder

研究组 & 干预措施

VRET

Experimental

Virtual Reality Exposure Therapy for agoraphobic participants

干预措施: Virtual Reality Exposure Therapy for agoraphobic participants (Behavioral)

Exposure in vivo

Active Comparator

Standard exposure in vivo for panic disorder

干预措施: Standard exposure in vivo for agoraphobic participants (Behavioral)

Wait-list control

No Intervention

Wait-list control group. Participants from this arm are randomized to the two active conditions after 10 weeks of waiting.

结局指标

主要结局

Panic Disorder Severity Scale (PDSS); Mobility Inventory for Agoraphobia (MI); Behavioural Avoidance Test (BAT)

时间窗: Assessed at pre- and post-treatment and 6-12 months follow-up

次要结局

  • Beck Anxiety Inventory (BAI); Anxiety Sensitivity Inventory (ASI); Beck Depression Inventory (BDI); Panic Disorder Severity Scale (PDSS); Agoraphobic Cognitions Questionnaire (ACQ); Bodily Sensations Questionnaire (BSQ); Panic Appraisal Inventory (PAI)(Process measures: are taken prior to treatment, after the fourth treatment session and at post-treatment. The PDSS and PAI will be administered every therapy session)

研究者

发起方
VU University of Amsterdam
申办方类型
Other
责任方
Principal Investigator
主要研究者

Paul M.G.Emmelkamp

Professor

VU University of Amsterdam

研究点 (1)

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