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认知行为疗法与接纳与承诺疗法(CBT-ACT)对比 COVID-19 危重症后的标准护理:一项试点随机对照试验方案

Cognitive Behavioral Therapy and Acceptance and Commitment Therapy (CBT-ACT) vs. Standard Care After Critical Illness Due to COVID-19: Protocol for a Pilot Randomized Controlled Trial.

作者信息

Håkansson Anders, Cronhjort Maria, Lidin-Darlington Pernilla, Lilja Gisela, Nilsson Anna, Schandl Anna, Friberg Hans

机构信息

Faculty of Medicine, Lund University, Lund, Sweden.

Clinical Research Unit, Department of Psychiatry, Malmø, Sweden.

出版信息

Front Psychiatry. 2022 Jul 15;13:907215. doi: 10.3389/fpsyt.2022.907215. eCollection 2022.

Abstract

BACKGROUND

Post-covid syndrome is an emerging condition involving a wide range of symptoms, including high rates of poor mental health. The diagnostic relevance and clinical severity of these symptoms are largely unknown, and evidence for treatment of post-covid mental health symptoms is lacking. This protocol describes a pilot randomized clinical trial, primarily aiming to assess feasibility, participant adherence and satisfaction in a novel phycho-therapeutic intervention on post-covid anxiety and depression symptoms ≥1 year after critically ill COVID-19. Whether the intervention may generate improvements in post-covid depression, anxiety, post-traumatic stress and health-related quality of life (HRQoL) will be addressed in a following larger trial.

METHODS

A multicenter, investigator-initiated randomized controlled trial (Clinical Trial Identifier number NCT05119608) including Intensive Care Unit (ICU)-treated COVID-19 survivors, who display symptoms of anxiety and/or depression at follow-up 12 months after hospitalization (Hospital Anxiety and Depression Scale ≥8 for depression or anxiety). Eligible individuals are referred to a psychiatrist for structured diagnostic assessment and inclusion in the trial. Participants will be randomized to either a 10-week cognitive behavioral therapy intervention with added acceptance and commitment therapy (CBT-ACT) or standard care (primary care referral). Primary study outcome measure is feasibility and patient adherence, defined as the proportion of participants who consent to randomization and remain in the study including follow-up. Secondary outcome measures include reduced symptoms in the HADS depression/anxiety subscales, post-traumatic symptoms, HRQoL and user satisfaction at 3 months after the intervention.

DISCUSSION

This protocol describes a pilot trial to assess feasibility and preliminary effects of a structured psycho-therapeutic intervention to ameliorate mental health in a population severely affected by COVID-19, where evidence for structured psycho-therapy is lacking.

摘要

背景

新冠后综合征是一种新出现的病症,涉及广泛的症状,包括心理健康状况不佳的比例较高。这些症状的诊断相关性和临床严重程度在很大程度上尚不清楚,且缺乏针对新冠后心理健康症状的治疗证据。本方案描述了一项试点随机临床试验,主要目的是评估对危重症新冠-19患者1年以上的新冠后焦虑和抑郁症状进行新型心理治疗干预的可行性、参与者的依从性和满意度。后续更大规模的试验将探讨该干预措施是否能改善新冠后的抑郁、焦虑、创伤后应激和健康相关生活质量(HRQoL)。

方法

一项多中心、研究者发起的随机对照试验(临床试验标识符编号NCT05119608),纳入在重症监护病房(ICU)接受治疗的新冠-19幸存者,这些患者在住院12个月后的随访中出现焦虑和/或抑郁症状(医院焦虑抑郁量表中抑郁或焦虑得分≥8)。符合条件的个体将被转介给精神科医生进行结构化诊断评估并纳入试验。参与者将被随机分为接受为期10周的认知行为疗法干预并附加接纳与承诺疗法(CBT-ACT)或标准护理(初级保健转诊)。主要研究结局指标是可行性和患者依从性,定义为同意随机分组并留在研究中包括随访的参与者比例。次要结局指标包括干预3个月后医院焦虑抑郁量表抑郁/焦虑子量表症状减轻、创伤后症状、健康相关生活质量和用户满意度。

讨论

本方案描述了一项试点试验,以评估在受新冠-19严重影响且缺乏结构化心理治疗证据的人群中,结构化心理治疗干预改善心理健康的可行性和初步效果。

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