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Examining the Effects of Different Resistive Exercise Programs in Individuals With Compensated Liver Cirrhosis

StatusNot Yet Recruiting
PhaseNot applicable
Started
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Record History

  1. Enrollment target: 30 to 20v2 Show 5 more changesShow less
    • Primary and study completion dates: Dec 23, 2025 to Dec 23, 2026
    • Start date: Dec 23, 2024 to Feb 19, 2026
    • Interventions: Assigned Interventions (Other), Control (Other), Face-to-face Exercise (Other), Home-based Exercise (Other) to Assigned Interventions (Other), Face-to-face Exercise (Other), Home-based Exercise (Other)
    • Site contact updated
    • Study arms: 3 to 2
  2. Study First Submitted
  • Stopped: an ongoing trial was terminated, suspended or withdrawn.
  • Notable: the trial’s plan changed such as a big move in its timeline or size, a new primary endpoint, sponsor or phase, or recruiting opened or resumed.
  • Minor: routine progress and housekeeping, such as sites added or enrollment closed.
Reasons such as sleep disorders, depression, decreased independence in daily living activities and decreased quality of life, which are seen in the majority of liver cirrhosis patients, can cause cognitive dysfunction, especially attention. It is known that physical dysfunctions are observed in patients with liver cirrhosis along with cognitive dysfunction. Sarcopenia is the most important of these dysfunctions. Sarcopenia is the progressive, widespread loss of muscle mass, function and strength. The aim of this study is to determine the effects of face-to-face and home-based progressive strengthening exercise program performed 3 times a week for 12 weeks on muscle strength, muscle mass, functionality and cognitive functions in individuals with liver cirrhosis. It is also aimed to test the feasibility and effectiveness of the home-based exercise method in individuals with liver cirrhosis. Another aim of our study is to determine the exercise dose required to improve muscle strength, muscle mass, functionality and cognitive functions in individuals with liver cirrhosis and the duration of treatment effectiveness through follow-up.
Trial Details
NCT Number NCT06749340
Lead Sponsor Bahçeşehir University
Conditions
(from sponsor)		 Coginitive Dysfunction, Compensated Liver Cirrhosis, Physical Dysfunction, Sarcopenia
Related terms Cognitive Dysfunction, Fibrosis, Sarcopenia
Enrollment 20 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov