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临床试验/NCT06337656
NCT06337656尚未招募不适用

Influence of an Alternating Whole-Body Vibration Training on Muscle Mass and Muscle Strength in Patients With Liver Cirrhosis and Sarcopenia: A Clinical Pilot Project

University Hospital of Cologne0 个研究点目标入组 15 人开始时间: 2024年6月1日最近更新:
适应症

试验速览

阶段
不适用
状态
尚未招募
发起方
入组人数
15
主要终点
Evaluation of the Effectiveness on muscle mass

研究概览

简要总结

  • Comprehensive Investigation of the Impact of Side-Alternating Whole-Body Vibration Training on Muscle Mass and Muscle Strength in Patients with Liver Cirrhosis and Sarcopenia
  • Simultaneous Characterization and Evaluation of Dynamic Changes in Health-Related Quality of Life in our Patient Cohort with Liver Cirrhosis and Sarcopenia through Side-Alternating Whole-Body Vibration Training.

研究设计

研究类型
Interventional
分配方式
Non Randomized
干预模型
Crossover
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

入选标准

  • Patients with confirmed or newly diagnosed compensated liver cirrhosis suffering from sarcopenia (combined decrease in muscle mass and muscle strength)
  • The liver cirrhosis is in a compensated stage.
  • The following etiologies of chronic liver disease are present: chronic hepatitis B infection, chronic hepatitis C infection, alcoholic liver disease, autoimmune hepatitis, cholestatic liver disease (PBC, PSC), or other chronic hepatopathy.
  • Alcohol abstinence of at least 3 months in cases of alcohol-related liver disease.
  • Routine cancer screening for the presence of a liver tumor (HCC surveillance) is routinely performed using MRI or CT scans, as ultrasound assessment is severely limited.
  • Permission from the treating physician to engage in physical activity.
  • Signed informed consent form.

排除标准

  • Non-compliance with inclusion criteria
  • Patients with recent hospitalizations (within the last 3 months) due to gastrointestinal bleeding, hepatic encephalopathy, or spontaneous bacterial peritonitis
  • Presence of inadequately treated portal hypertension
  • Known chronic liver disease not described in the above groups
  • Alcohol consumption >20 g per day
  • Excessive alcohol consumption during the study period leads to exclusion from the study
  • Substance abuse
  • Taking medications known to affect muscle mass or strength (e.g., Amiodarone, Chloroquine, Macrolides)
  • Taking medications known to cause movement disorders (e.g., Reserpine, Lithium, Cyclosporine A, Dopamine agonists)
  • Patients with unstable cardiovascular diseases: e.g., unstable angina pectoris, uncontrolled hypertension (≥ 160/100 mmHg), uncontrolled diabetes (blood sugar > 250 mg/dl), history of myocardial infarction or stroke
  • Patients with musculoskeletal deformities, symptomatic rheumatoid or osteoarthritis
  • Patients with untreated or newly diagnosed active malignant tumors in history
  • Patients with neuromuscular or neurodegenerative diseases
  • Patients with untreated hernias
  • Patients with symptomatic, known untreated aortic aneurysm, with recent hospitalizations (within the last 6 months)
  • Patients with fractures within the last 12 months
  • Participation in moderate-intensity training programs for more than 2 hours per week
  • Patients who have received chemotherapy at the time of the study or in the past 3 months
  • Other underlying conditions that contraindicate vibration training and/or functional performance tests
  • Circumstances preventing the individual from assessing the nature, scope, and possible consequences of the clinical trial
  • Signs indicating that the subject is likely not to adhere to the study protocol (e.g., lack of cooperation)
  • a. Definition of hepatic decompensation
  • Occurrence of symptomatic ascites, hepatic encephalopathy, portal hypertensive bleeding (e.g., esophageal variceal bleeding), infection

结局指标

主要结局

Evaluation of the Effectiveness on muscle mass

时间窗: 6 months

Evaluation of the Effectiveness on muscle mass through quantification of muscle mass by the skeletal muscle index (SMI) at the level of lumbar vertebral body 3 measured in MRI or CT.

Evaluation of the Effectiveness on muscle thickness

时间窗: 6 months

Evaluation of the Effectiveness on muscle mass through quantification of muscle mass by the transverse psoas muscle thickness (TPMT) at the level of lumbar vertebral body 3 measured in MRI or CT.

Evaluation of the Effectiveness on physical function

时间窗: 6 months

Evaluation of the Effectiveness on physical function by using the Liver-Frailty-Index

Evaluation of the Effectiveness on mobility, in particular the risk of falling

时间窗: 6 months

Evaluation of the Effectiveness on mobility, in particular the risk of falling by using the Tinetti test

Evaluation of the Effectiveness on muscle strength

时间窗: 6 months

Evaluation of the effectiveness of the intervention in terms of muscle strength using the hand-grip-strength

次要结局

  • Evaluation of Safety of the Training Method(12 weeks)
  • Health-Related Quality of Life(6 months)

研究者

发起方
University Hospital of Cologne
申办方类型
Other
责任方
Principal Investigator
主要研究者

Eva Dittmann

Principal Investigator

University Hospital of Cologne

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