Leavy Breiffni, Kwak Lydia, Hagströmer Maria, Franzén Erika
Department of Neurobiology, Care Sciences and Society, Division of Physiotherapy, Karolinska Institute, Huddinge, Sweden.
Stockholms Sjukhem Foundation, Stockholm, Sweden.
BMC Neurol. 2017 Feb 7;17(1):27. doi: 10.1186/s12883-017-0809-2.
If people with progressive neurological diseases are to avail of evidence-based rehabilitation, programs found effective in randomized controlled trials (RCT's) must firstly be adapted and tested in clinical effectiveness studies as a means of strengthening their evidence base. This paper describes the protocol for an effectiveness-implementation trial that will assess the clinical effectiveness of a highly challenging balance training program (the HiBalance program) for people with mild-moderate Parkinson's disease (PD) while simultaneously collecting data concerning the way in which the program is implemented. The HiBalance program is systemically designed to target balance impairments in PD and has been shown effective at improving balance control and gait in a previous RCT. Study aims are to i) determine the effectiveness of the adapted HiBalance program on performance and self-rated outcomes such as balance control, gait and physical activity level ii) conduct a process evaluation of program implementation at the various clinics iii) determine barriers and facilitators to program implementation in these settings.
This effectiveness-implementation type 1 hybrid study will use a non-randomized controlled design with consecutive inclusion of people with PD at multiple clinical sites. A mixed method approach will be used to collect clinical effectiveness data and process evaluation data which is both quantitative and qualitative in nature. The consolidated framework for implementation research (CFIR) will be used to guide the planning and collection of data concerning implementation barriers and facilitators. The HiBalance program will be provided by physical therapists as a part of standard rehabilitation care at the clinical sites, while the evaluation of the implementation process will be performed by the research group and funded by research grants.
An effectiveness-implementation study design benefits patients by speeding up the process of translating findings from research settings to routine health care. Findings from this study will also be highly relevant for those working with neurological rehabilitation when faced with decisions concerning the translation of training programs from efficacy studies to everyday clinical practice.
ClinicalTrials.gov march 2016, NCT02727478 .
如果患有进行性神经疾病的患者要采用循证康复,那么在随机对照试验(RCT)中被证明有效的方案首先必须在临床有效性研究中进行调整和测试,以此来加强其证据基础。本文描述了一项有效性-实施试验的方案,该试验将评估一项极具挑战性的平衡训练方案(HiBalance方案)对轻-中度帕金森病(PD)患者的临床有效性,同时收集有关该方案实施方式的数据。HiBalance方案是系统设计的,旨在针对PD患者的平衡障碍,并且在之前的一项RCT中已被证明能有效改善平衡控制和步态。研究目的包括:i)确定调整后的HiBalance方案对平衡控制、步态和身体活动水平等表现及自我评定结果的有效性;ii)对各诊所的方案实施进行过程评估;iii)确定这些环境中方案实施的障碍和促进因素。
这项有效性-实施1型混合研究将采用非随机对照设计,在多个临床地点连续纳入PD患者。将使用混合方法收集临床有效性数据和过程评估数据,这些数据兼具定量和定性性质。实施研究的整合框架(CFIR)将用于指导有关实施障碍和促进因素的数据规划和收集。HiBalance方案将由物理治疗师在临床地点作为标准康复护理的一部分提供,而实施过程的评估将由研究小组进行,并由研究资助提供资金。
有效性-实施研究设计通过加快将研究结果转化为常规医疗保健的过程,使患者受益。本研究的结果对于从事神经康复工作的人员在面对将训练方案从疗效研究转化为日常临床实践的决策时也将具有高度相关性。
ClinicalTrials.gov 2016年3月,NCT02727478 。