BMJ Open Gastroenterol. 2024 Sep 3;11(1):e001410. doi: 10.1136/bmjgast-2024-001410.
Physical frailty is associated with increased mortality and poor quality of life (QoL) before and after liver transplantation (LT). Evidence is lacking on how to tailor exercise and behavioural techniques in this patient population.
Home-based EXercise and motivAtional programme before and after Liver Transplantation (EXALT) is a phase 2b, open-label, two-centre randomised controlled clinical trial designed to investigate whether a remotely monitored 'home-based exercise and theory-based motivation support programme (HBEP)' before and after LT improves QoL in LT recipients. Adult patients awaiting a primary LT will be assessed for eligibility at two LT centres (Birmingham, Royal Free London). Participants will be randomly assigned (1:1) to receive either an HBEP while on the LT waiting list through to 24 weeks after LT (Intervention) or a patient exercise advice leaflet (Control). Using a standard method of difference in means (two-sided significance level 0.05; power 0.90) and accounting for a 35% attrition/withdrawal rate, a minimum of 133 patients will be randomised to each treatment group. The primary outcome measure will be assessed using intention-to-treat analysis of the difference in the Physical Component Score of Short form-36 version 2.0 health-related QoL questionnaire between the groups at 24 weeks post-LT.
The protocol was approved by the South Central-Hampshire A National Research Ethics Committee. Recruitment into the EXALT trial started in May 2022 and is due to end in June 2024, with 217/266 patients randomised to date. The intervention follow-up is due to finish in May 2026. The findings of this trial will be disseminated through peer-reviewed publications, conferences and social media.
ISRCTN13476586.
在肝移植(LT)之前和之后,身体虚弱与死亡率增加和生活质量(QoL)下降有关。缺乏关于如何针对这一患者群体调整运动和行为技术的证据。
肝移植前后家庭锻炼和动机计划(EXALT)是一项 2b 期、开放标签、两中心随机对照临床试验,旨在研究 LT 前和 LT 后远程监测的“家庭锻炼和基于理论的动机支持计划(HBEP)”是否能改善 LT 受者的 QoL。等待进行原发性 LT 的成年患者将在两个 LT 中心(伯明翰皇家自由伦敦)进行资格评估。参与者将通过 LT 等待名单随机分配(1:1)接受 HBEP,直至 LT 后 24 周(干预组)或患者运动建议传单(对照组)。使用均值差异的标准方法(双侧显著性水平 0.05;功率 0.90),并考虑到 35%的损耗/退出率,将对每组至少 133 名患者进行随机分组。主要结局测量将使用 SF-36 版本 2.0 健康相关 QoL 问卷的物理成分评分在 LT 后 24 周时两组之间的意向治疗分析进行评估。
该方案已获得南中汉普郡 A 国家伦理委员会的批准。EXALT 试验的招募工作于 2022 年 5 月开始,预计将于 2024 年 6 月结束,截至目前已有 217/266 名患者随机分组。干预随访预计于 2026 年 5 月结束。该试验的结果将通过同行评审的出版物、会议和社交媒体进行传播。
ISRCTN81244463。