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I-WOTCH研究的过程评估方案:一项针对慢性非恶性疼痛患者的阿片类药物减量支持计划。

Process evaluation protocol for the I-WOTCH study: an opioid tapering support programme for people with chronic non-malignant pain.

作者信息

Nichols Vivien P, Abraham Charles, Eldabe Sam, Sandhu Harbinder K, Underwood Martin, Seers Kate

机构信息

Warwick Clinical Trials Unit, Warwick Medical School, University of Warwick, Coventry, UK

Faculty of Medicine, Dentistry and Health Sciences, University of Melbourne, Melbourne, UK.

出版信息

BMJ Open. 2019 Oct 10;9(10):e028998. doi: 10.1136/bmjopen-2019-028998.

Abstract

INTRODUCTION

The Improving the Wellbeing of people with Opioid Treated CHronic Pain (I-WOTCH) randomised controlled trial uses a multicomponent self-management intervention to help people taper their opioid use. This approach is not widely used and its efficacy is unknown. A process evaluation alongside the trial will help to assess how the intervention was delivered, looking at the dose of intervention received and the fidelity of the delivery. We will explore how the intervention may have brought about change through the experiences of the participants receiving and the staff delivering the intervention and whether there were contextual factors involved.

METHODS AND ANALYSIS

A mixed methods process evaluation will assess how the processes of the I-WOTCH intervention fared and whether these affected the outcomes. We will collect quantitative data, for example, group attendance analysed with statistical methods. Qualitative data, for example, from interviews and feedback forms will be analysed using framework analysis. We will use a 'following a thread' and a mixed methods matrix for the final integrated analysis.

ETHICS AND DISSEMINATION

The I-WOTCH trial and process evaluation were granted full ethics approval by Yorkshire and The Humber-South Yorkshire Research Ethics Committee on 13 September 2016 (16/YH/0325). All data were collected in accordance with data protection guidelines. Participants provided written informed consent for the main trial, and all interviewees provided additional written informed consent. The results of the process evaluation will be published and presented at conferences.

TRIAL REGISTRATION NUMBER

ISRCTN49470934; Pre-results.

摘要

引言

改善阿片类药物治疗慢性疼痛患者的健康状况(I-WOTCH)随机对照试验采用多成分自我管理干预措施,以帮助人们减少阿片类药物的使用。这种方法并未广泛应用,其疗效尚不清楚。在试验过程中进行的过程评估将有助于评估干预措施的实施方式,观察所接受的干预剂量以及实施的保真度。我们将通过接受干预的参与者和提供干预的工作人员的经历,探索干预措施可能如何带来改变,以及是否涉及背景因素。

方法与分析

一项混合方法的过程评估将评估I-WOTCH干预措施的实施过程情况以及这些过程是否影响了结果。我们将收集定量数据,例如,用统计方法分析小组出勤情况。定性数据,例如来自访谈和反馈表的数据,将使用框架分析法进行分析。我们将使用“顺藤摸瓜”法和混合方法矩阵进行最终的综合分析。

伦理与传播

I-WOTCH试验和过程评估于2016年9月13日获得约克郡和亨伯 - 南约克郡研究伦理委员会的全面伦理批准(16/YH/0325)。所有数据均按照数据保护指南收集。参与者为主要试验提供了书面知情同意书,所有受访者均提供了额外的书面知情同意书。过程评估的结果将在会议上发表和展示。

试验注册号

ISRCTN49470934;预结果。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/43a5/6797361/e59f62b8d3c3/bmjopen-2019-028998f01.jpg

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