FIT4Cirrhotics@Home: Effects of a Home-based Bimodal Lifestyle Intervention in Patients With Liver Cirrhosis Awaiting Orthotopic Liver Transplantation
试验速览
- 阶段
- 不适用
- 状态
- 尚未招募
- 入组人数
- 16
- 试验地点
- 2
- 主要终点
- Aerobic capacity
研究概览
简要总结
Chronic liver disease eventually results in liver cirrhosis and is associated with an increasing deterioration in patients' physical fitness. As there is currently limited evidence regarding the effects of a home-based exercise program in patients with liver cirrhosis awaiting OLT, and physical frailty rates are particularly high in this patient population, this group has the investigators specific interest. The primary aim of this study is to assess the effect of a semi-supervised home-based bimodal lifestyle program, consisting of interval and endurance training and peripheral resistance training on aerobic capacity in patients with liver cirrhosis awaiting OLT
详细描述
Rationale: Patients with liver cirrhosis who are on the waiting list for orthotopic liver transplantation (OLT) encounter all key components of physical frailty, i.e., decreased functional capacity, impaired aerobic capacity and sarcopenia, which all lead to fatigue, diminished quality of life, increased hospitalization and pre- and post-transplantation morbidity and mortality. An exercise program in combination with nutritional support has proven to improve all key components of physical frailty and quality of life in various surgical patient populations. Although small studies have demonstrated similar positive effects of exercise training in patients on the waiting list for OLT, to date no large studies supported the effects of exercise training and nutritional support on (the longevity of) the increase in aerobic capacity in OLT patients.
Objective: The primary objective of this study is to assess the effect of a semi-supervised home based bimodal lifestyle intervention on aerobic capacity (measured by VO2 at the Ventilatory anaerobic threshold (VAT) and VO2peak in ml/kg/min) in patients with liver cirrhosis on the waiting list for OLT. Secondary objectives are to evaluate individual patients' responses to the bimodal lifestyle intervention on sarcopenia, anthropometry, functional mobility, quality of life, perceived fatigue, incidence of hepatic encephalopathy, number of unplanned hospital admissions, change in liver frailty index score and change in microbiome composition at six, 12 and 18 weeks, or until transplantation. Finally, the feasibility (participation rate, reasons for non-participation, adherence/compliance, dropout rate, reasons for dropout and adverse event) will be assessed.
Study design: This study is an investigator-initiated, single center, single arm, prospective clinical trial. It will take place at the University Medical Center Groningen, the Netherlands. Eligible patients will participate in the bimodal lifestyle program, which comprises two home-based training periods of six-weeks each (12 weeks training in total, or until transplantation). After 18 weeks (i.e., six weeks after termination of the program) a final assessment will take place to evaluate the longevity of the expected effects of the lifestyle program on predefined study outcomes.
Study population: Adult patients diagnosed with liver cirrhosis and screened for OLT, with a VO2 at the VAT ≤13ml/kg/min and/or VO2peak ≤18ml/kg/min will be screened for potential eligibility. Patients with no contraindications to physical exercise training and the ability to work out on a cycle ergometer can participate in the bimodal lifestyle intervention.
Intervention: Patients will participate in a home-based bimodal lifestyle program. The program comprises semi-supervised high intensity interval and endurance training on an advanced cycle ergometer (Lode Corival Home+ , Lode BV, Groningen, The Netherlands), combined with nutritional support consisting of protein, vitamin and mineral supplementation. Moreover, to improve functional mobility and muscle function patients will perform peripheral resistance training of the large muscle groups of the upper and lower extremities. Finally, to improve respiratory performance after surgery and potentially reduce pulmonary complications, patients will perform breathing exercises. The program will be patient personalized and compromises three training sessions per week. The cycle ergometer used for this program will upload training results of the interval and endurance training sessions to an online platform, enabling remote monitoring of patients' adherence and training progress. Furthermore, a community physical therapist will visit the patient at least weekly to monitor progress and to optimize the training intensity.
研究设计
- 研究类型
- Interventional
- 分配方式
- Na
- 干预模型
- Single Group
- 主要目的
- Treatment
- 盲法
- None
入排标准
- 年龄范围
- 18 Years 至 —(Adult, Older Adult)
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Aged at least 18 years;
- •Diagnosed with end-stage liver disease / liver cirrhosis (regardless of etiology);
- •On the waiting list for OLT;
- •VO2 at the VAT ≤13 ml/kg/min and/or VO2peak ≤18 ml/kg/min;
- •Speaks the Dutch language;
- •Understands the purpose of the study and has given written informed consent to participate in the study.
排除标准
- •Experienced a MACE (e.g., myocardial infarction) in the past six months;
- •Experienced a cerebrovascular incident in the past six months;
- •Medical history of an uncontrolled heart rhythm disorder;
- •Hepatic encephalopathy grade 3 or 4;
- •Acute liver failure;
- •Acute on chronic liver failure;
- •Hospitalization at start of the study;
- •Non-treated esophageal varices (i.e., variceal eradication endoscopy and/or adequately dosed NSBB);
- •MELD score ≥30;
- •Not capable of cycling on a cycle ergometer;
- •No available community physical therapist in the living area of the patient.
- •Patients refusing or unable to sign informed consent
结局指标
主要结局
Aerobic capacity
时间窗: During baseline measurements patients will perform a cardiopulmonary exercise test to determine their baseline aerobic capacity. After 6 weeks of home-based training the cardiopulmonary exercise test will be repeated to reassess their aerobic capacity.
The main study parameter/endpoint is the change in aerobic capacity after the first six weeks of the FIT4Cirrhotics@Home program, for which the following outcomes will be assessed: VO2 at the VAT (ml/kg/min). A cardiopulmonary exercise test will be performed by participants to determine their aerobic capacity pre-intervention and after six weeks of training.
次要结局
- Functional mobility assessment(through study completion, an average of 1 year)
- Quality of Life assessment(through study completion, an average of 1 year)
- Anthropometry assessment(through study completion, an average of 1 year)
- Incidence of hepatic encephalopathy assessment(through study completion, an average of 1 year)
- Postoperative outcomes up to 12 months post-OLT assessment(through study completion, and up to 12 months post-OLT assessment)
- Ultrasound measurements of muscle thickness(through study completion, an average of 1 year)
- Perceived fatigue assessment(through study completion, an average of 1 year)
- Liver frailty index score assessment(During through study completion, an average of 1 year and immediately post-intervention)
- Number and reasons for intercurrent hospitalizations assessment(through study completion, an average of 1 year)
- Microbiome composition assessment(through study completion, an average of 1 year)
