膝关节骨性关节炎患者的自我调节训练:可行性随机对照试验(MiNT 试验)方案

Ramakrishnan Mani, D. Adhia, Sharon Awatere, Andrew Robert Gray, Jerin Mathew, Luke Charles Wilson, Amanda Still, David Jackson, Ben Hudson, Fadel Zeidan, Roger Fillingim, Dirk De Ridder
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摘要

膝关节骨关节炎(OA)是一种慢性继发性肌肉骨骼疼痛,会导致残疾、生活质量下降和高昂的社会成本。与膝关节 OA 相关的疼痛与大脑感觉、认知和情感区域的敏感性增加有关。针对与疼痛体验相关的大脑功能进行自我调节训练可以减轻疼痛及其相关的残疾。正念冥想(MM)和脑电神经反馈(EEG-NF)训练等自我调节疗法可改善膝关节OA患者的临床疗效。可行性临床试验可以解决一些因素,为全面试验的设计提供参考,调查自我调节训练计划对膝关节OA患者的有效性。该临床试验将评估自我调节训练计划的可行性、安全性、可接受性、体验和认知。拟议的可行性试验基于双盲(结果评估者和调查者)、三臂(MM 常规护理组、EEG-NF + 常规护理组和常规护理对照组)随机对照平行临床试验。患有膝关节 OA 的参与者将从社区和医疗机构招募。一名研究助理(RA)将实施两种干预措施(20 分钟疗程,每周四次,连续三周共 12 次疗程)。将记录干预措施的可行性(参与者招募率、干预措施坚持率、保留率)、安全性和可接受性。对组别分配保密的 RA 将记录基线、干预后即刻(第 4 周)和干预后 3 个月的次要结果。定量结果测量将进行描述性总结。定性访谈将评估参与者对试验各方面的体验和看法,包括确定参与试验的障碍和促进因素,评估他们对研究程序的意见,如对研究地点的偏好,以及确定干预措施作为治疗膝关节OA的潜在临床疗法的可接受程度。此外,还将探讨毛利人的世界观如何接受评估和训练实践。该试验将为膝关节OA患者接受MM和EEG-NF训练的可行性、安全性和可接受性提供证据,从而为全面随机临床对照试验的设计提供参考。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Self-regulation training for people with knee osteoarthritis: a protocol for a feasibility randomised control trial (MiNT trial)
Knee osteoarthritis (OA) is a chronic secondary musculoskeletal pain condition resulting in disability, reduced quality of life, and high societal costs. Pain associated with knee OA is linked to increased sensitivity in sensory, cognitive, and emotional areas of the brain. Self-regulation training targeting brain functioning related to pain experience could reduce pain and its associated disability. Self-regulatory treatments such as mindfulness meditation (MM) and electroencephalography neurofeedback (EEG-NF) training improve clinical outcomes in people with knee OA. A feasibility clinical trial can address factors that could inform the design of the full trial investigating the effectiveness of self-regulation training programmes in people with knee OA. This clinical trial will evaluate the feasibility, safety, acceptability, experience and perceptions of the self-regulatory training programmes.The proposed feasibility trial is based on a double-blind (outcome assessor and investigators), three-arm (MM usual care, EEG-NF + usual care and usual care control group) randomised controlled parallel clinical trial. Participants with knee OA will be recruited from the community and healthcare practices. A research assistant (RA) will administer both interventions (20-min sessions, four sessions each week, and 12 sessions over three successive weeks). Feasibility measures (participant recruitment rate, adherence to interventions, retention rate), safety, and acceptability of interventions will be recorded. An RA blinded to the group allocation will record secondary outcomes at baseline, immediately post-intervention (4th week), and 3 months post-intervention. The quantitative outcome measures will be descriptively summarised. The qualitative interviews will evaluate the participants' experiences and perceptions regarding various aspects of the trial, which includes identifying the barriers and facilitators in participating in the trial, evaluating their opinions on the research procedures, such as their preferences for the study site, and determining the level of acceptability of the interventions as potential clinical treatments for managing knee OA. Māori participant perceptions of how assessment and training practices could be acceptable to a Māori worldview will be explored. The interviews will be audio-recorded and analysed thematically.This trial will provide evidence on the feasibility, safety, and acceptability of the MM and EEG-NF training in people with knee OA, thus informing the design of a full randomised clinical control trial.
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