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一种用于可卡因戒断期依赖的新型疗法:一项随机临床试验。

A Novel Therapy for cocaine dependence during abstinence: A randomized clinical trial.

作者信息

Pirnia Bijan, Moradi Ali Reza, Pirnia Kambiz, Kolahi Parisa, Roshan Rasool

机构信息

Ph.D. Student of Clinical Psychology, Department of Psychology, Faculty of Humanities, University of Science and Culture, Tehran, Iran.

Ph.D. of Psychology, Professor, Department of Psychology, Faculty of Humanities, Kharazmi University, Tehran, Iran.

出版信息

Electron Physician. 2017 Jul 25;9(7):4862-4871. doi: 10.19082/4862. eCollection 2017 Jul.

Abstract

BACKGROUND

Topiramate is an anticonvulsant drug and an ideal candidate for reducing the craving in people relying on cocaine. Contingency management is one of the common therapies in the domain of addiction.

OBJECTIVE

The present study aimed to evaluate and compare three medication methods of Topiramate (TPM), Contingency Management (CM) and the combined TPM treatment and cash intervention on craving during abstinence.

METHODS

This randomized clinical trial was conducted at Bijan Center for Substance Abuse Treatment in Tehran, Iran, from December 15, 2014 to November 20, 2015. One hundred males (Age range=18-34; SD=4.11) undergoing abstinence were assigned randomly to four groups (n=25) of Topiramate (TPM), Contingency Management (CM) and the Combined Method plus a placebo control group. Treatment was provided for twelve weeks for the experiment groups, and only the control group received the placebo. Participants in the Cash-based and CM Condition had an identical 12-week escalating schedule of reinforcement (cash-based incentives worth $0, $20, $40, and $80). Also, in the Topiramate group, participants' dosage ranged between 25-300 mg/day in escalating doses) 25, 50, 100, 150, 200, 250, 300). In addition, all subjects received brief behavioral compliance enhancement treatment (BBCET). Participants took a urine test twice a week, with a given threshold of > 300 ng/ml, and indicators of cocaine craving (response rate= 91%) was evaluated in two phases of pre-test and post-test. We used Chi square, ANCOVA Univariate Model and Scheffe's post hoc to analyze the primary and secondary outcomes. Also, the qualitative data resulted from demographic evaluations were coded and analyzed by the instrument of analysis of qualitative data i.e. Atlas.ti, Version 5.2.

RESULTS

The results showed that all three types of treatment played a significant efficacy in reducing the craving. The mean (95% CI) scores of craving was 12.04 (p=0.05) with TPM, 13.89 (p=0.05) with CM, 10.92 (p=0.01) with Mix and 16.89 (p>0.05) with control. Moreover, the highest variance explaining the changes in craving was assigned to the combined treatment (p<0.01).

CONCLUSIONS

The findings of this study, while having applicable aspects in this domain, can be helpful in planning supplementary remedial procedures.

TRIAL REGISTRATION

The trial was registered at the Thai Clinical Trial Registration Center with the TCR ID: TCTR20170112001.

FUNDING

The authors received no financial support for the research, authorship, and/or publication of this article.

摘要

背景

托吡酯是一种抗惊厥药物,是减少可卡因依赖者渴望的理想候选药物。应急管理是成瘾领域的常见治疗方法之一。

目的

本研究旨在评估和比较托吡酯(TPM)、应急管理(CM)以及TPM联合现金干预这三种药物治疗方法对戒毒期间渴望的影响。

方法

这项随机临床试验于2014年12月15日至2015年11月20日在伊朗德黑兰的Bijan药物滥用治疗中心进行。100名正在戒毒的男性(年龄范围=18 - 34岁;标准差=4.11)被随机分为四组(每组n = 25),分别为托吡酯组(TPM)、应急管理组(CM)、联合治疗组以及安慰剂对照组。实验组接受为期12周的治疗,只有对照组接受安慰剂。基于现金和CM条件的参与者有相同的为期12周的强化递增计划(价值0美元、20美元、40美元和80美元的现金奖励)。此外,在托吡酯组中,参与者的剂量范围为每天25 - 300毫克(递增剂量为25、50、100、150、200、250、300毫克)。所有受试者均接受简短行为依从性增强治疗(BBCET)。参与者每周进行两次尿液检测,给定阈值> 300纳克/毫升,并在测试前和测试后两个阶段评估可卡因渴望指标(反应率= 91%)。我们使用卡方检验、协方差分析单变量模型和谢费尔事后检验来分析主要和次要结果。此外,由人口统计学评估得出的定性数据通过定性数据分析工具即Atlas.ti 5.2版本进行编码和分析。

结果

结果表明,所有三种治疗方法在减少渴望方面均具有显著疗效。托吡酯组渴望的平均(95%置信区间)评分为12.04(p = 0.05),CM组为13.89(p = 0.05),联合治疗组为10.92(p = 0.01),对照组为16.89(p>0.05)。此外,解释渴望变化的最大方差归因于联合治疗(p<0.01)。

结论

本研究结果在该领域具有应用价值,有助于规划补充性补救程序。

试验注册

该试验在泰国临床试验注册中心注册,注册号为TCTR20170112001。

资金

作者未获得该研究、撰写和/或发表本文的资金支持。

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引用本文的文献

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Electron Physician. 2016 Nov 25;8(11):3214-3221. doi: 10.19082/3214. eCollection 2016 Nov.
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