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基于接纳的行为疗法促进HIV接纳、HIV信息披露及医疗服务留存率的初步随机对照试验

Pilot Randomized Controlled Trial of Acceptance-Based Behavior Therapy to Promote HIV Acceptance, HIV Disclosure, and Retention in Medical Care.

作者信息

Moitra Ethan, LaPlante Andrea, Armstrong Megan L, Chan Philip A, Stein Michael D

机构信息

Warren Alpert Medical School of Brown University, Box G-BH, Providence, RI, 02912, USA.

Louisiana State University - Health Sciences Center, New Orleans, LA, 70112, USA.

出版信息

AIDS Behav. 2017 Sep;21(9):2641-2649. doi: 10.1007/s10461-017-1780-z.

Abstract

HIV patients who are not retained in medical care risk viral resistance, disease progression to AIDS, and mortality. Numerous interventions have been tested to improve retention, but they are limited by their resource-intensive approaches and lack of focus on new patients, who are at highest risk for drop-out. Data show that acceptance and disclosure of HIV status might impact retention, yet these variables have not been targeted in previous interventions. In this pilot randomized controlled trial, we assessed feasibility, acceptability, and preliminary efficacy of a brief, 2-session acceptance based behavior therapy (ABBT), relative to treatment-as-usual (TAU), in 34 new-to-care HIV patients. ABBT attendance was high and patient feedback was positive. Relative to TAU, ABBT had significant positive effects on retention, as well as putative mechanisms of action, including experiential avoidance of HIV, willingness to make and actual disclosures of HIV status, and perceived social support. Further testing of ABBT is warranted. Trial registered at clinicaltrials.gov; Clinical Trial #NCT02004457.

摘要

未持续接受医疗护理的艾滋病病毒感染者面临病毒耐药、疾病进展为艾滋病以及死亡的风险。为提高留存率,人们已对多种干预措施进行了测试,但这些措施因资源密集型方法以及缺乏对新患者(即退出风险最高的患者)的关注而受到限制。数据表明,艾滋病病毒感染状况的接受度和披露情况可能会影响留存率,但在以往的干预措施中尚未针对这些变量。在这项试点随机对照试验中,我们评估了一种简短的、分两阶段的基于接纳的行为疗法(ABBT)相对于常规治疗(TAU),对34名新接受治疗的艾滋病病毒感染者的可行性、可接受性和初步疗效。ABBT的参与率很高,患者反馈也很积极。相对于TAU,ABBT对留存率以及假定的作用机制有显著的积极影响,这些机制包括对艾滋病病毒的经验性回避、对艾滋病病毒感染状况进行披露的意愿和实际披露情况,以及感知到的社会支持。有必要对ABBT进行进一步测试。该试验已在clinicaltrials.gov注册;临床试验编号:#NCT02004457。

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