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临床试验/NCT01900301
NCT01900301已完成1 期

Cholinergic Decontextualization of Exposure Therapy for Anxiety

University of California, Los Angeles1 个研究点 分布在 1 个国家目标入组 60 人开始时间: 2013年8月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
1 期
状态
已完成
入组人数
60
试验地点
1
主要终点
Subjective Units of Distress

研究概览

简要总结

Fear, whether it occurs in humans suffering from an anxiety disorder or in experimental models with rodents, is reduced by exposing the frightened organism to the fearful stimulus in the absence of any negative consequences (i.e., extinction, or exposure therapy). However, fear often renews when the feared stimulus is encountered in a context different from the exposure context. In rats, the investigators found that interfering with the animal's ability to process contexts during extinction by administering an anticholinergic drug prevented fear renewal. This proposal will determine if the beneficial effect of this drug translates to exposure therapy in socially anxious humans. To this end, 100 individuals with Social Phobia who fear public speaking will undergo repeated sessions of exposure to public speaking, within a virtual reality context. Participants will be randomized to either drug placebo, .4mg/.01 mL Scopolamine, .5mg/.01 mL Scopolamine or .6mg/.01 mL Scopolamine, administered via nasal drops, prior to each session of exposure therapy. One month after completion of exposure therapy, context renewal will be tested by comparing physiological and subjective responses to public speaking in the same virtual context as used during exposure therapy versus a context different than the one used during exposure therapy. The goal is to identify the dose of Scopolamine associated with the greatest reduction in context renewal. In addition, a secondary analysis will attempt to identify those individuals who benefit most from Scopolamine-augmentation of exposure therapy.

研究设计

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

入排标准

年龄范围
18 Years 至 55 Years(Adult)
性别
All
接受健康志愿者

入选标准

  • between the ages of 18 and 55,
  • fluent in English,
  • within normal body weight (BMI=18.5 to 24.9)
  • meet DSM-IV diagnostic criteria for Social Phobia and report a fear of public speaking.

排除标准

  • participant report of a diagnosed medical or neurological disorder
  • prescription or over the counter medications that can interact with Scopolamine, such as anticholinergic medications (e.g. belladonna alkaloids, antihistamines, meclizine, tricyclic antidepressants, and muscle relaxants), cold medicines, cough suppressants. Other drugs that will be reasons for exclusion include: antimuscarinics, nifedipine, parasympathomimetics, amantadine, amoxapine, antacids, antidiarrheals, anxiolytics, hypnotics, atomexetine, bupropion, cisapride, clozapine, cyclobenzaprine, digoxin, disopyramide, dronabinol (THC), ethanol, maprotilline, memantine, metoclopramide, nabilone, olanzapine, opiate agonists, orphenadrine, phenothiazines, potassium salts, quinidine, sedating H1-blockers, topiramate, tricyclic antidepressants, erthyromycin, ketoconazole, and tegaserod.
  • over the counter drugs or substances that may have a sedative effect (e.g. herbal sedatives: ashwagandha, Duboisia hopwoodii, Prostanthera striatiflora, kava, mandrake, valerian, cannabis, passiflora incarnate; Antihistamines: Diphenhydramine, Dimenhydrinate, Doxylamine, Promethazine; Alcohol; Dextromethorphan)
  • individuals with urinary problems (e.g., BPH)
  • pregnant or nursing females (as the effect of Scop on fetuses is not known)
  • suicidality
  • delusions or hallucinations
  • history of substance dependence in last five years or substance abuse within the past 6 months

研究组 & 干预措施

Scopolamine .4mg

Experimental

Participants will be randomized to either .4mg/.01 mL Scopolamine, .5mg/.01 mL Scopolamine or .6mg/.01 mL Scopolamine, administered via nasal drops, prior to each session of exposure therapy

干预措施: Scopolamine (Drug)

Intranasal placebo

Placebo Comparator

Participants will be randomized to a placebo, administered via nasal drops, prior to each session of exposure therapy

干预措施: intranasal placebo (Drug)

Scopolamine .5mg

Experimental

Participants will be randomized to either .4mg/.01 mL Scopolamine, .5mg/.01 mL Scopolamine or .6mg/.01 mL Scopolamine, administered via nasal drops, prior to each session of exposure therapy

干预措施: Scopolamine (Drug)

Scopolamine .6mg

Experimental

Participants will be randomized to either .4mg/.01 mL Scopolamine, .5mg/.01 mL Scopolamine or .6mg/.01 mL Scopolamine, administered via nasal drops, prior to each session of exposure therapy

干预措施: Scopolamine (Drug)

结局指标

主要结局

Subjective Units of Distress

时间窗: change from final exposure session to follow-up (8 weeks following baseline)

Skin conductance responses and heart rate

时间窗: change from final exposure session to follow-up (8 weeks following baseline)

Eye blink startle reflex

时间窗: change from final exposure session to follow-up (8 weeks following baseline)

次要结局

  • Self Statements During Public Speaking Scale(change from baseline to follow-up (8 weeks following baseline))
  • Personal Report of Confidence as a Speaker Scale(change from baseline to follow-up (8 weeks following baseline))
  • Subjective units of distress during in vivo speech(change from baseline to follow-up (8 weeks following baseline))

研究者

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

Michelle Craske

Professor, Department of Psychology

University of California, Los Angeles

研究点 (1)

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