一项试验(quality - swat)中定性方法学研究的方案开发:karma - deep -2试验。

HRB open research Pub Date : 2023-11-20 eCollection Date: 2023-01-01 DOI:10.12688/hrbopenres.13721.2
John McCaffrey, Andrew Hunter
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引用次数: 0

摘要

背景:尽管临床试验的设计和实施在方法学上有所改进,但有关精神卫生保健的试验仍然存在方法学上的局限性。在karma - deep -2宿主试验中,将进行一项定性研究(quality - swat),以探索和理解精神卫生保健随机试验中的两个方法学问题:(1)参与精神卫生随机试验的主要障碍和推动因素是什么;(2)随机试验如何成为常规精神卫生保健的一部分。这些问题将根据优先研究主题,从患者-参与者和临床医生/研究人员-参与者的角度进行检查。方法:采用描述性定性研究设计。数据将通过一对一的半结构化访谈收集,由微软团队进行。访谈数据将使用布劳恩和克拉克的主题分析方法进行分析。将对三个参与者组(N = 30)进行一对一访谈:1)主持试验的患者-参与者(N = 10);2)可能符合条件的宿主试验患者-拒绝纳入宿主试验的参与者(n = 10);3)与宿主试验相关的临床医生/研究人员参与者(n = 10)。伦理和传播:爱尔兰圣帕特里克精神卫生服务研究伦理委员会(参考:第09/20号议定书)批准了伦理批准。研究完成后,将编写一份报告并提交给卫生研究委员会(HRB)。研究结果将与主办试验团队和研究参与者共享,并提交发表。主试验注册:ClinicalTrials.gov (NCT04939649);草案(2019-003109-92)。官方标题:氯胺酮作为重度抑郁症的辅助治疗-一项随机对照试验:[KARMA-Dep(2)]。
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Protocol Development for a Qualitative Methodological Study Within a Trial (Qual-SWAT): The KARMA-Dep-2 Trial.

Background: Despite methodological improvements in clinical trial design and conduct more generally, methodological limitations persist in trials concerning mental health care. A qualitative Study Within A Trial (Qual-SWAT), embedded in the KARMA-Dep-2 host trial, will be undertaken to explore and gain an understanding of two methodological questions in randomised trials specific to mental health care: (1) what are the key barriers and enablers of participation in randomised trials in mental health; and (2) how can randomised trials become part of routine mental health care. These issues will be examined from patient-participant and clinician- / researcher-participant perspectives, in alignment with PRioRiTy research themes.

Methods: A descriptive qualitative study design will be used. Data will be collected via one-to-one semi-structured interviews, conducted via Microsoft Teams. The interview data will be analysed using Braun and Clarke's Thematic Analysis approach. One-to-one interviews will be conducted with three participant groups ( N = 30): 1) host trial patient-participants ( n = 10); 2) potentially eligible host trial patient-participants who refused enrolment in the host trial ( n = 10); and 3) clinician- / researcher-participants who are associated with work on the host trial ( n = 10).

Ethics and dissemination: Ethical approval has been granted by St. Patrick's Mental Health Services Research Ethics Committee, Ireland (Ref: Protocol 09/20). When the study is completed, a report will be prepared and submitted to the Health Research Board (HRB). Findings will be shared with the host trial team and study participants, and submitted for publication.

Host trial registration: ClinicalTrials.gov ( NCT04939649); EudraCT ( 2019-003109-92). Official title: Ketamine as an Adjunctive Therapy for Major Depression - A Randomised Controlled Trial: [KARMA-Dep (2)].

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