Eyre V, Lang C C, Smith K, Jolly K, Davis R, Hayward C, Wingham J, Abraham C, Green C, Warren F C, Britten N, Greaves C J, Doherty P, Austin J, Van Lingen R, Singh S, Buckingham S, Paul K, Taylor R S, Dalal H M
Peninsula Clinical Trials Unit, Plymouth University, Plymouth, UK.
School of Medicine, University of Dundee, Ninewells Hospital and Medical School, Dundee, UK.
BMJ Open. 2016 Oct 25;6(10):e012853. doi: 10.1136/bmjopen-2016-012853.
The Rehabilitation EnAblement in CHronic Heart Failure in patients with Heart Failure (HF) with preserved ejection fraction (REACH-HFpEF) pilot trial is part of a research programme designed to develop and evaluate a facilitated, home-based, self-help rehabilitation intervention to improve self-care and quality of life (QoL) in heart failure patients and their caregivers. We will assess the feasibility of a definitive trial of the REACH-HF intervention in patients with HFpEF and their caregivers. The impact of the REACH-HF intervention on echocardiographic outcomes and bloodborne biomarkers will also be assessed.
A single-centre parallel two-group randomised controlled trial (RCT) with 1:1 individual allocation to the REACH-HF intervention plus usual care (intervention) or usual care alone (control) in 50 HFpEF patients and their caregivers. The REACH-HF intervention comprises a REACH-HF manual with supplementary tools, delivered by trained facilitators over 12 weeks. A mixed methods approach will be used to assess estimation of recruitment and retention rates; fidelity of REACH-HF manual delivery; identification of barriers to participation and adherence to the intervention and study protocol; feasibility of data collection and outcome burden. We will assess the variance in study outcomes to inform a definitive study sample size and assess methods for the collection of resource use and intervention delivery cost data to develop the cost-effectiveness analyses framework for any future trial. Patient outcomes collected at baseline, 4 and 6 months include QoL, psychological well-being, exercise capacity, physical activity and HF-related hospitalisation. Caregiver outcomes will also be assessed, and a substudy will evaluate impact of the REACH-HF manual on resting global cardiovascular function and bloodborne biomarkers in HFpEF patients.
The study is approved by the East of Scotland Research Ethics Service (Ref: 15/ES/0036). Findings will be disseminated via journals and presentations to clinicians, commissioners and service users.
ISRCTN78539530; Pre-results .
射血分数保留的心力衰竭(HFpEF)患者慢性心力衰竭康复赋能(REACH-HFpEF)试点试验是一项研究计划的一部分,该计划旨在开发和评估一种便捷的、基于家庭的自助康复干预措施,以改善心力衰竭患者及其照护者的自我护理和生活质量(QoL)。我们将评估在HFpEF患者及其照护者中进行REACH-HF干预确定性试验的可行性。还将评估REACH-HF干预对超声心动图结果和血源性生物标志物的影响。
一项单中心平行两组随机对照试验(RCT),将50例HFpEF患者及其照护者按1:1个体分配至REACH-HF干预加常规护理(干预组)或仅接受常规护理(对照组)。REACH-HF干预包括一本REACH-HF手册及辅助工具,由经过培训的协调员在12周内提供。将采用混合方法评估招募和保留率的估计;REACH-HF手册交付的保真度;确定参与和坚持干预及研究方案的障碍;数据收集的可行性和结果负担。我们将评估研究结果的方差,以确定确定性研究的样本量,并评估收集资源使用和干预交付成本数据的方法,以建立未来任何试验的成本效益分析框架。在基线、4个月和6个月收集的患者结果包括生活质量、心理健康、运动能力、身体活动和与HF相关的住院情况。还将评估照护者的结果,并且一项子研究将评估REACH-HF手册对HFpEF患者静息整体心血管功能和血源性生物标志物的影响。
该研究已获得苏格兰东部研究伦理服务机构批准(参考编号:15/ES/0036)。研究结果将通过期刊和向临床医生、专员及服务使用者的汇报进行传播。
ISRCTN78539530;预结果 。