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电针对迁延性安非他命戒断综合征的疗效:一项实用随机对照试验的研究方案。

Electro-acupuncture for protracted amphetamine abstinence syndrome: study protocol for a pragmatic randomized controlled trial.

机构信息

School of Acupuncture-Moxibustion and Tuina, Chengdu University of Traditional Chinese Medicine, Chengdu, Sichuan, 610075, China.

Coercive Rehabilitation Center for Addicts Affiliated to the Public Security Bureau of Deyang, Deyang, Sichuan, 618007, China.

出版信息

Trials. 2022 Mar 15;23(1):216. doi: 10.1186/s13063-022-06154-7.

Abstract

BACKGROUND

Protracted amphetamine abstinence syndrome is one of the primary causes of relapse for amphetamine-type drug abusers during withdrawal. However, the importance of the management of protracted amphetamine abstinence syndrome is underestimated. Electro-acupuncture may be a safe and effective alternative therapy for protracted amphetamine abstinence syndrome, but the evidence is limited.

METHODS

The study is a prospective, two-center, randomized, waitlist controlled, open-label pragmatic trial. A total of 300 patients with protracted amphetamine abstinence syndrome will be recruited. All participants will be randomly assigned to an electro-acupuncture group or a waitlist group in a 1:1 ratio. Participants in the electro-acupuncture group will receive the electrical-acupuncture treatment. Waitlist group participants will not receive electro-acupuncture treatment but will be assessed at each visit. Treatments will be administered twice a week for a total of 4 consecutive weeks. The primary outcome in this study is the change in the ACSA between baseline (week 0) and the completion of treatment (week 4), and the secondary outcomes are changes in the Hamilton Depression Scale (HAMD), the visual analog scale (VAS), the Hamilton Anxiety Scale (HAMA), the Pittsburgh Sleep Quality Index (PSQI), the Montreal Cognitive Assessment (MoCA), and the Medical Outcomes Study 36-item Short-Form Health Survey (SF-36).

DISCUSSION

This study will assess the effectiveness of acupuncture in PAAS in real-world settings to provide support for clinical decisions and a basis for subsequent trials comparing acupuncture with other positive regimens.

TRIAL REGISTRATION

ClinicalTrials.gov ChiCTR2000040619 . Registered on 3 December 2020.

摘要

背景

迁延性安非他命戒断综合征是安非他命类药物滥用者戒断期间复吸的主要原因之一。然而,迁延性安非他命戒断综合征的管理重要性被低估了。电针可能是迁延性安非他命戒断综合征的一种安全有效的替代治疗方法,但证据有限。

方法

本研究是一项前瞻性、两中心、随机、等待对照、开放标签实用临床试验。共招募 300 例迁延性安非他命戒断综合征患者。所有参与者将以 1:1 的比例随机分配到电针组或等待组。电针组患者将接受电针治疗。等待组患者将不接受电针治疗,但将在每次就诊时进行评估。治疗将每周进行两次,共连续 4 周。本研究的主要结局是基线(第 0 周)和治疗完成时(第 4 周)之间 ACSA 的变化,次要结局是汉密尔顿抑郁量表(HAMD)、视觉模拟量表(VAS)、汉密尔顿焦虑量表(HAMA)、匹兹堡睡眠质量指数(PSQI)、蒙特利尔认知评估(MoCA)和医疗结局研究 36 项简短健康调查(SF-36)的变化。

讨论

本研究将在真实环境中评估针刺治疗 PAAS 的有效性,为临床决策提供支持,并为后续比较针刺与其他阳性方案的试验提供基础。

试验注册

ClinicalTrials.gov ChiCTR2000040619 。于 2020 年 12 月 3 日注册。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a6b7/8922742/0f72b9f4aaab/13063_2022_6154_Fig1_HTML.jpg

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