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针对精神分裂症或相关障碍患者的阿凡达疗法。

Avatar Therapy for people with schizophrenia or related disorders.

作者信息

Aali Ghazaleh, Kariotis Timothy, Shokraneh Farhad

机构信息

Cochrane Schizophrenia Group, Institute of Mental Health, The University of Nottingham, Nottingham, UK.

School of Computing and Information Systems, University of Melbourne, Parkville, Melbourne, Australia.

出版信息

Cochrane Database Syst Rev. 2020 May 8;5(5):CD011898. doi: 10.1002/14651858.CD011898.pub2.

Abstract

BACKGROUND

Many people with schizophrenia do not achieve satisfactory improvements in their mental state, particularly the symptom of hearing voices (hallucinations), with medical treatment.

OBJECTIVES

To examine the effects of Avatar Therapy for people with schizophrenia or related disorders.

SEARCH METHODS

In December 2016, November 2018 and April 2019, the Cochrane Schizophrenia Group's Study-Based Register of Trials (including registries of clinical trials) was searched, review authors checked references of all identified relevant reports to identify more studies and contacted authors of trials for additional information.

SELECTION CRITERIA

All randomised clinical trials focusing on Avatar Therapy for people with schizophrenia or related disorders.

DATA COLLECTION AND ANALYSIS

We extracted data independently. For binary outcomes, we calculated risk ratio (RR) and 95% confidence intervals (CI), on an intention-to-treat basis. For continuous data, we estimated the mean difference (MD) between groups and 95% CIs. We employed a fixed-effect model for analyses. We assessed risk of bias for included studies and created 'Summary of findings' tables using GRADE. Our main outcomes of interest were clinically important change in; mental state, insight, global state, quality of life and functioning as well as adverse effects and leaving the study early.

MAIN RESULTS

We found 14 potentially relevant references for three studies (participants = 195) comparing Avatar Therapy with two other interventions; treatment as usual or supportive counselling. Both Avatar Therapy and supportive counselling were given in addition (add-on) to the participants' normal care. All of the studies had high risk of bias across one or more domains for methodology and, for other risks of bias, authors from one of the studies were involved in the development of the avatar systems on trial and in another trial, authors had patents on the avatar system pending. 1. Avatar Therapy compared with treatment as usual When Avatar Therapy was compared with treatment as usual average endpoint Positive and Negative Syndrome Scale - Positive (PANSS-P) scores were not different between treatment groups (MD -1.93, 95% CI -5.10 to 1.24; studies = 1, participants = 19; very low-certainty evidence). A measure of insight (Revised Beliefs about Voices Questionnaire; BAVQ-R) showed an effect in favour of Avatar Therapy (MD -5.97, 95% CI -10.98 to -0.96; studies = 1, participants = 19; very low-certainty evidence). No one was rehospitalised in either group in the short term (risk difference (RD) 0.00, 95% CI -0.20 to 0.20; studies = 1, participants = 19; low-certainty evidence). Numbers leaving the study early from each group were not clearly different - although more did leave from the Avatar Therapy group (6/14 versus 0/12; RR 11.27, 95% CI 0.70 to 181.41; studies = 1, participants = 26; low-certainty evidence). There was no clear difference in anxiety between treatment groups (RR 5.54, 95% CI 0.34 to 89.80; studies = 1, participants = 19; low-certainty evidence). For quality of life, average Quality of Life Enjoyment and Satisfaction Questionnaire-Short Form (QLESQ-SF) scores favoured Avatar Therapy (MD 9.99, 95% CI 3.89 to 16.09; studies = 1, participants = 19; very low-certainty evidence). No study reported data for functioning. 2. Avatar Therapy compared with supportive counselling When Avatar Therapy was compared with supportive counselling (all short-term), general mental state (Psychotic Symptom Rating Scale (PSYRATS)) scores favoured the Avatar Therapy group (MD -4.74, 95% CI -8.01 to -1.47; studies = 1, participants = 124; low-certainty evidence). For insight (BAVQ-R), there was a small effect in favour of Avatar Therapy (MD -8.39, 95% CI -14.31 to -2.47; studies = 1, participants = 124; low-certainty evidence). Around 20% of each group left the study early (risk ratio (RR) 1.06, 95% CI 0.59 to 1.89; studies = 1, participants = 150; moderate-certainty evidence). Analysis of quality of life scores (Manchester Short Assessment of Quality of Life (MANSA)) showed no clear difference between groups (MD 2.69, 95% CI -1.48 to 6.86; studies = 1, participants = 120; low-certainty evidence). No data were available for rehospitalisation rates, adverse events or functioning.

AUTHORS' CONCLUSIONS: Our analyses of available data shows few, if any, consistent effects of Avatar Therapy for people living with schizophrenia who experience auditory hallucinations. Where there are effects, or suggestions of effects, we are uncertain because of their risk of bias and their unclear clinical meaning. The theory behind Avatar Therapy is compelling but the practice needs testing in large, long, well-designed, well-reported randomised trials undertaken with help from - but not under the direction of - Avatar Therapy pioneers.

摘要

背景

许多精神分裂症患者经药物治疗后,其精神状态,尤其是幻听(幻觉)症状,并未得到令人满意的改善。

目的

研究阿凡达疗法对精神分裂症或相关障碍患者的疗效。

检索方法

2016年12月、2018年11月和2019年4月,检索了Cochrane精神分裂症研究组基于研究的试验注册库(包括临床试验注册库),综述作者检查了所有已识别的相关报告的参考文献以识别更多研究,并联系试验作者以获取更多信息。

入选标准

所有针对精神分裂症或相关障碍患者的阿凡达疗法的随机临床试验。

数据收集与分析

我们独立提取数据。对于二分类结局,我们在意向性分析的基础上计算风险比(RR)和95%置信区间(CI)。对于连续性数据,我们估计组间平均差(MD)和95%CI。我们采用固定效应模型进行分析。我们评估了纳入研究的偏倚风险,并使用GRADE创建了“结果总结”表。我们感兴趣的主要结局是临床上重要的变化;精神状态、洞察力、整体状态、生活质量和功能,以及不良反应和提前退出研究。

主要结果

我们找到了三项研究(参与者 = 195)的14篇潜在相关参考文献,这些研究将阿凡达疗法与其他两种干预措施进行了比较;常规治疗或支持性咨询。阿凡达疗法和支持性咨询都是在参与者的常规护理基础上额外提供的(附加)。所有研究在方法学的一个或多个领域都存在高偏倚风险,对于其他偏倚风险,其中一项研究的作者参与了试验中阿凡达系统的开发,在另一项试验中,作者拥有正在申请专利的阿凡达系统。1. 阿凡达疗法与常规治疗的比较 当将阿凡达疗法与常规治疗进行比较时,治疗组之间的平均终点阳性和阴性症状量表 - 阳性(PANSS-P)得分没有差异(MD -1.93,95%CI -5.10至1.24;研究 = 1,参与者 = 19;极低确定性证据)。一项洞察力测量(修订后的幻听信念问卷;BAVQ-R)显示有利于阿凡达疗法的效果(MD -5.97,95%CI -10.98至 -0.96;研究 = 1,参与者 = 19;极低确定性证据)。短期内两组均无人再次住院(风险差(RD)0.00,95%CI -0.20至0.20;研究 = 1,参与者 = 19;低确定性证据)。每组提前退出研究的人数没有明显差异 - 尽管阿凡达疗法组退出的人数更多(6/14对0/12;RR 11.27,95%CI 0.70至181.41;研究 = 1,参与者 = 26;低确定性证据)。治疗组之间的焦虑没有明显差异(RR 5.54,95%CI 0.34至89.80;研究 = 1,参与者 = 19;低确定性证据)。对于生活质量,平均生活质量享受和满意度问卷 - 简表(QLESQ-SF)得分有利于阿凡达疗法(MD 9.99,95%CI 3.89至16.09;研究 = 1,参与者 = 19;极低确定性证据)。没有研究报告功能方面的数据。2. 阿凡达疗法与支持性咨询的比较 当将阿凡达疗法与支持性咨询(均为短期)进行比较时,总体精神状态(精神病症状评定量表(PSYRATS))得分有利于阿凡达疗法组(MD -4.74,95%CI -8.01至 -1.47;研究 = 1,参与者 = 124;低确定性证据)。对于洞察力(BAVQ-R),有一个有利于阿凡达疗法的小效果(MD -8.39,95%CI -14.31至 -2.47;研究 = 1,参与者 = 124;低确定性证据)。每组约20%的人提前退出研究(风险比(RR)1.06,95%CI 0.59至1.89;研究 = 1,参与者 = 150;中度确定性证据)。生活质量得分(曼彻斯特生活质量简短评估(MANSA))分析显示两组之间没有明显差异(MD 2.69,95%CI -1.48至6.86;研究 = 1,参与者 = 120;低确定性证据)。没有关于再次住院率、不良事件或功能的数据。

作者结论

我们对现有数据的分析表明,对于有幻听的精神分裂症患者,阿凡达疗法几乎没有一致的效果(如果有的话)。在存在效果或效果迹象的情况下,由于其偏倚风险和不明确的临床意义,我们并不确定。阿凡达疗法背后的理论很有说服力,但实践需要在阿凡达疗法先驱者的帮助下(但不是在其指导下)进行大规模、长期、设计良好、报告完善的随机试验来检验。

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