hypfast试验研究方案:一项II期、单中心、开放标签的随机对照试验,比较原发性高血压患者早期限时喂养与标准护理对血压控制的影响

A. Valentini, J. E. Loyola, Joice Inglez, R. Ferreira, J. Souza, Juan Santana-Guerrero, Daniela Yucumá, V. Liutti, Salma Abdelrahman, Michelle Pirazzoli, N. Kaegi-Braun, H. Reyes, Islam G. Ahmed, Hiba Elhiday, A. Guimarães, J. Oller, M. Friend, Jéssica Sanches, Álvaro Sierra Mencia, A. Kann, M. Rosa
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摘要

:背景:原发性动脉高压是全球最常见的慢性病,对公众健康有重大影响。据推测,16:8的早期限时进食(eTRF)有助于血压管理。到目前为止,还没有随机试验评估其在高血压治疗中的益处作为主要结果。目的:确定eTRF联合生活方式改变是否优于2018年欧洲高血压指南推荐的标准生活方式改变治疗原发性高血压。方法:这将是一项优越的、平行的、开放标签的、随机的II期试验,在瑞士苏黎世的一个中心进行。参与者年龄在30至60岁之间,最近被诊断为高正常和一级高血压,将被随机分配到eTRF 18:6加生活方式改变组或标准生活方式干预组。主要结果是八周时的平均收缩压与基线测量值之间的差异。讨论:这将是第一项评估原发性高血压患者间歇性禁食效果的试验。潜在的限制包括患者对干预的依从性。然而,在之前的一项研究中,1351名参与者中有1128人(83.50%)自我报告了依从性。此外,本研究还寻求提高依从性的策略。结论:我们希望这项试验能指导其他作者进行未来的研究,以期获得更高的外部有效性,并评估间歇性禁食治疗原发性高血压的长期效果。
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HYP-FAST trial study protocol: a phase II, single-center, open-label RCT comparing the effect of early time-restricted feeding on blood pressure control versus standard of care in individuals with primary hypertension
: Background : Primary arterial hypertension is the most prevalent chronic disease globally and significantly impacts public health. It is hypothesized that 16:8 early time-restricted feeding (eTRF) bolsters blood pressure management. To date, there are no randomized trials evaluating its benefits in the treatment of hypertension as a primary outcome. Objective: To determine if eTRF combined with lifestyle modifications is superior to the standard lifestyle modifications treatment of primary hypertension recommended by the 2018 European hypertension guidelines. Methods: This will be a superiority, parallel, open-label, randomized, phase II trial carried out in a single center in Zurich, Switzerland. Participants between 30 and 60 years of age, recently diagnosed with high normal and grade I hypertension will be randomly assigned to the eTRF 18:6 plus lifestyle modifications group or the standard lifestyle interventions group. The primary outcome will be the difference between the mean systolic blood pressure at eight weeks with the baseline measurement. Discussion: This will be the first trial to evaluate the effects of intermittent fasting in patients with primary hypertension. Potential limitations include patient compliance to the intervention. However, in a previous study, self-reported adherence was observed in 1128 of 1351 participants (83.50%). In addition, this study seeks strategies to improve adherence. Conclusion: We hope that this trial directs other authors to carry out future studies aiming for higher external validity and evaluation of long-term effects of intermittent fasting for the treatment of primary hypertension.
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