LiveSMART Trial to Prevent Falls in Patients With Cirrhosis
Phase 3
Completed
NCT05794555
| Condition | Cirrhosis, Liver, Portal Hypertension |
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| Phase | Phase 3 |
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| Sponsor | University of Michigan |
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| Status | Completed |
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| Enrollment | 233 participants |
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| Interventions | Enhanced Usual Care, Lactulose, Investigator recommended exercise, TeleTai-Chi (virtual) |
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| Start date | Jun 13, 2023 |
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| Completion date | Mar 7, 2025 |
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| Results posted | Jul 31, 2026 |
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Summary
This multicenter trial is being conducted to determine if sequential lactulose and Tele (virtual) Tai-Chi reduces the rate of injurious fall, non-injurious falls, incident overt Hepatic Encephalopathy (HE), and death or liver transplant over 24 weeks. Participants that are enrolled will be randomized to stage one of this project for approximately 12 weeks. After completing stage one, participants will be re-randomized to stage 2 of the project that will last approximately 12 more weeks. The study hypothesizes that sequential lactulose/TeleTai-Chi will reduce falls, incident overt HE, death and physical frailty and will improve cognitive function, and Health Related Quality of Life (HRQOL) over 24 weeks compared to other treatment combinations. As detailed below, an observational component that enrolls caregivers of the trial participants is being conducted. Upon completion, Participants listed in the record here only include trial participants; and the observational component was moved to a new registration for clarity, NCT07140120.
Number of Participants Experiencing a Hierarchical Composite of Events Over 24 Weeks: Injurious Falls, Non-injurious Falls, Incident Hepatic Encephalopathy, Liver Transplant, and Death/Transplant
Baseline to 24 weeks · Participants
| Treatment (Lactulose) Plus Enhanced Usual Care Then TeleTai-Chi Exercise Classes | 11 Participants |
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| Treatment (Lactulose) Plus Enhanced Usual Care Then Recommended Exercise | 10 Participants |
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| Enhanced Usual Care Group Followed by Tele-Tai Chi Exercise Classes | 14 Participants |
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| Enhanced Usual Care Group Followed by Investigator Recommended Exercise | 29 Participants |
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Open in BENITIONS
View on ClinicalTrials.gov
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