跳至主要内容
临床试验/NL-OMON52802
NL-OMON52802招募中3 期

IMPROVE: Improving anxiety treatment by Modulating emotional memories PRiOr to in Vivo Exposure: A randomized controlled trial. - IMPROVE - Modulating emotional memories: a RCT

niversiteit Utrecht0 个研究点目标入组 50 人开始时间: 待定最近更新:
适应症

试验速览

阶段
3 期
状态
招募中
入组人数
50

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional

入排标准

年龄范围
18 至 64(—)

入选标准

  • - Patients of >18 years of age
  • - Sufficient mastery of the Dutch language to complete questionnaires
  • - Ability to understand questionnaires and written informed consent
  • - Meeting DSM-5 criteria for primary panic disorder (with or without
  • agoraphobia) (assessed with MINI-S-DSM-5)
  • - Stable medication for at least six weeks and willingness by the patient and
  • physician to keep the medication stable during the study period (until FU1).
  • The use of sedating medication (e.g. benzodiazepines) is no contraindication,
  • however participants are strongly advised not to use sedating medication prior
  • to- or after treatment sessions and subsequent days. Use of sedating medication
  • will be registered
  • - Willingness and ability not to be under the influence of alcohol or drugs
  • twenty-four hours before and after each session, general use will be
  • discouraged as much as possible

排除标准

  • - Neurological disorder
  • - Acute or recent history of suicide attempts according to the M.I.N.I. section
  • - Self-reported visual or auditory impairments that could hinder treatment
  • - Self-reported epilepsy, pregnancy, or heart disease (these are common
  • exclusion criteria for using a fear conditioning task, see 8.3.3)
  • - Not willing or able to fill in (online) questionnaires.

研究者

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