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一项关于体外冲击波治疗糖尿病足溃疡愈合的探索性三臂随机对照试验及定性研究(SOLEFUL):研究方案

A Pilot Three Arm Randomised Controlled Trial and Qualitative Study of Extracorporeal Shockwave Therapy for Diabetic Foot Ulcer Healing (SOLEFUL): A Study Protocol.

作者信息

Hitchman L, Iglesias C, Russell D, Smith G, Twiddy M, Chetter I C

机构信息

Faculty of Clinical Sciences, Hull York Medical School, Hull, UK.

Department of Health Sciences, University of York, York, England.

出版信息

Int Wound J. 2025 Apr;22(4):e70176. doi: 10.1111/iwj.70176.

Abstract

The development of effective interventions for diabetes-related foot ulcers (DFU) healing is vital. This protocol outlines a pilot trial and qualitative study investigating ESWT in DFU healing. A pilot three arm placebo controlled double-blinded randomised controlled trial. Participants with a DFU will be randomised to high dose (500 shocks/cm), low dose (100 shocks/cm) or sham ESWT, in addition to standard care. The primary outcome will be deliverability of a definitive trial. Secondary outcomes are ulcer healing, quality-of-life and healthcare resource use at 6 months. The target sample size is 90 participants. The study is registered on clinicaltrials.gov, reference: NCT05380544 and has ethical approval (REC reference: 22/WA/0089). The qualitative interview study will recruit participants who complete, drop-out and decline to participate in the pilot trial, and healthcare professionals who deliver DFU care. Maximum variable sampling will be used to recruit participants. Data will be analysed with an inductive exploratory approach using reflexive thematic analysis. The pilot trial will ensure methods used will address the research question in the definitive trial. The qualitative study will explore how patients and clinicians interact with the trial to understand the pilot trial findings.

摘要

开发有效的糖尿病相关足部溃疡(DFU)愈合干预措施至关重要。本方案概述了一项关于探讨体外冲击波疗法(ESWT)对DFU愈合影响的试点试验和定性研究。这是一项三臂安慰剂对照双盲随机对照试点试验。患有DFU的参与者除接受标准护理外,将被随机分为高剂量(500次冲击/平方厘米)、低剂量(100次冲击/平方厘米)或假ESWT组。主要结局将是确定性试验的可行性。次要结局包括6个月时的溃疡愈合情况、生活质量和医疗资源使用情况。目标样本量为90名参与者。该研究已在clinicaltrials.gov上注册,参考编号:NCT05380544,并已获得伦理批准(REC参考编号:22/WA/0089)。定性访谈研究将招募完成、退出和拒绝参与试点试验的参与者,以及提供DFU护理的医疗专业人员。将采用最大可变抽样法招募参与者。数据将采用归纳探索性方法,通过反思性主题分析进行分析。试点试验将确保所使用的方法能解决确定性试验中的研究问题。定性研究将探讨患者和临床医生如何与试验互动,以理解试点试验的结果。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b929/11955253/4c321646c722/IWJ-22-e70176-g001.jpg

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