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临床试验/NCT01399866
NCT01399866已完成3 期

Cognitive Remediation With D-cycloserine to Improve Smoking Cessation Outcomes

Massachusetts General Hospital1 个研究点 分布在 1 个国家目标入组 150 人开始时间: 2011年5月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
3 期
状态
已完成
入组人数
150
试验地点
1
主要终点
Effect of D-cycloserine + Cue-exposure Treatment on Continuous Abstinence From Tobacco Smoking.

研究概览

简要总结

One hundred seventy-five eligible participants will be enrolled with aim of randomizing 60 to a double-blind, placebo-controlled trial of D-cycloserine added to cue-exposure treatment to prevent relapse to smoking. Subjects who sign an informed consent, meet inclusion criteria, and demonstrate response to cue reactivity at the screening visit, will either be:

  • started on approximately 3 weeks of either nicotine replacement therapy (NRT) at a dose of either 14 or 21 mg/day or varenicline titrated to 1.0 mg bid; decision of which method to use to quit smoking will be based on participant choice as well as taking into account any medical contraindications to either therapy.
  • evaluated to confirm abstinence from smoking. Recently abstinent participants referred by a smoking cessation clinic, PCP or self referred must have an expired air CO < 10 ppm to confirm abstinence.

Subjects who are able to demonstrate 18-24 hours of abstinence prior to the first Cue Exposure Therapy Visit (CET I) will be eligible to be randomized to two visits of study medication and cue exposure treatment, spaced five to nine days apart. Subjects will complete 2 follow-up visits at 2-4 days and four weeks after the last CET visit. The entire study involves twelve visits and will last approximately ten weeks. For recently abstinent participants referred by a smoking cessation clinic, PCP or self referred, the study involves 7 visits (screening and baseline visit will be merged into one and there is no CBT component) and will last approximately 7 weeks.

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, Care Provider, Investigator)

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

  • Participants must have smoked an average of ≥ 10 cigarettes/day during the past 6 months
  • have expired air CO ≥ 10 ppm or urine cotinine ≥ 100 ng/mL
  • meet DSM-IV criteria for nicotine dependence
  • aged 18 - 65
  • Recently abstinent participants referred by a PCP, smoking cessation clinic or self referred must have an expired air CO < 10 ppm to confirm abstinence

排除标准

  • Severe or uncontrolled medical or psychiatric illness
  • History of multiple hospitalizations within the last six months for an ongoing medical condition
  • Any significant, current and unstable cardiovascular disease, end stage renal failure, severe COPD requiring oxygen, any current unstable neurological disease, a history of seizures or epilepsy, or a history of head trauma with lasting neurological sequelae, will be excluded for their safety.
  • Major depressive episode, mania or mixed episode in the prior 6 months
  • Lifetime history of psychosis, delusional disorder, organic mental disorder by DSM-IV criteria, or ongoing cognitive impairment will also be excluded for their safety,
  • Current excessive use of alcohol (>21 drinks/week in female subjects; >28 drinks/week in male subjects)
  • Current use of illicit drugs.
  • Current steroid use, current, daily use of benzodiazepines, or participants who are unwilling to modify their benzodiazepine use will.
  • Pregnant or breastfeeding women will be excluded, as well as women of childbearing potential who will not use a medically acceptable method of contraception (i.e. IUD, oral contraceptives).
  • Participants who are deaf, blind, or experience any other significant sensory impairment that would preclude them from completing study procedures will also be excluded, as well as participants who are unable to understand study procedures or provide informed consent.
  • Participants receiving isoniazid or ethionamide, or who have a known sensitivity to D-cycloserine.

研究组 & 干预措施

Placebo

Placebo Comparator

50 mg capsule,single dose, twice, one week apart, by mouth

干预措施: Placebo (Drug)

D-cycloserine

Active Comparator

50 mg capsule,single dose, twice, one week apart, by mouth

干预措施: D-cycloserine (Drug)

结局指标

主要结局

Effect of D-cycloserine + Cue-exposure Treatment on Continuous Abstinence From Tobacco Smoking.

时间窗: Up to 6 weeks

Participants assigned to receive D-cycloserine + CET will achieve better maintenance of tobacco abstinence, as assessed with self-report and saliva cotinine measurements, than those who receive placebo + CET at week 6 follow up visits

次要结局

  • Effect of D-cycloserine + Cue-exposure Treatment on Skin Conductance(6 weeks)
  • Effect of D-cycloserine + Cue-exposure Treatment on Attentional Bias Toward Smoking Cuesmeasured With the Emotional Stroop Task(Baseline and week 6)
  • Effect of D-cycloserine + Cue-exposure Treatment on Heart Rate(6 weeks)
  • Effect of D-cycloserine + Cue-exposure Treatment on Electromyogram(6 weeks)
  • Effect of D-cycloserine + Cue-exposure Treatment on Craving(6 weeks)

研究者

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

A. Eden Evins

Director Center for Addiction Medicine

Massachusetts General Hospital

研究点 (1)

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