Clinical Trials Directory

Trials / Completed

CompletedNCT06163001

Role of Exercise in Chronic Liver Disease Patients Undergoing Liver Transplantation

Effects of Supervised Aerobic and Resistance Exercises on Measures of Frailty in Chronic Liver Disease Patients Undergoing Living Donor Liver Transplantation- an Open Label Randomised Controlled Trial

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
60 (actual)
Sponsor
Institute of Liver and Biliary Sciences, India · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

The goal of this randomised clinical trial (open label) is to test the effect of supervised aerobic and resistance exercises in chronic liver disease patients being planned for living donor liver transplantation (LDLT). The main question it aims to answer are: * If pre-operative supervised aerobic and resistance exercise for 4 weeks can improve the measures of frailty (Liver frailty index, Short physical performance battery, pulmonary function tests) in chronic liver disease patients being planned for LDLT. * Can this approach also translate into clinically significant benefits in the postoperative outcomes of LDLT. Participants will be randomised into two groups receiving either 1. Standard medical therapy along with supervised aerobic and resistance exercises for 4 weeks. 2. Standard medical therapy. The two groups will be compared for progression of the measures of frailty ver the course of their participation as well as their post LDLT outcomes.

Detailed description

1. Aim and Objective - Primary objective: To assess effects of pre-operative aerobic and resistance exercises in decompensated CLD patients planned for LDLT on the measures of frailty after 1 month of supervised exercise. Secondary objectives: To assess effects of pre-operative aerobic and resistance exercises in decompensated CLD patients planned for LDLT on the post LDLT outcomes, myostatin levels (on POD 14) and skeletal muscle mass (on POD14). 2. Methodology: * Study population - Consecutive voluntary adults (\>18 years) with chronic liver disease, planned for living donor liver transplantation fulfilling the conditions as per inclusion and exclusion criteria. * Study design - Interventional study- Open label randomised controlled trial * Study period - From time of ethical clearance till 31st December 2024 * Sample size - Assuming median LFI for CLD patients as 3.9 ± 0.3\*, and assuming an improvement of 5% with introduction of exercise along with SMT after 1 follow up, and keeping alpha of 5%, and power of study as 90%, with 1:1 ratio of cases and controls, then by method of change we need to enroll a total of 54 patients with 27 in each arm. Assuming 10% non compliance, a total of 60 cases will be enrolled, with 30 cases in each arm. * Intervention - Pre-operative supervised exercise-based regimen versus standard medical therapy alone for a minimum duration of 4 weeks. * Monitoring and assessment - Clinical profile of the patient and symptoms will be serially followed during the patients OPD visits. * Adverse effects - Exercise may aggravate encephalopathy, metabolic disorders, AKI/HRS. It may also lead to falls due to cardio-pulmonary intolerance or hepatic encephalopathy. * Stopping rule - Inability to follow the exercise schedule, or development of any of the adverse effects due to exercise as mentioned above. 3. Expected outcome of the project: Better values of measures of frailty and post LDLT outcomes in patients receiving pre-operative concurrent exerises as an intervention.

Conditions

Interventions

TypeNameDescription
BEHAVIORALSupervised aerobic and resistance exercises4 weeks of preoperative supervised aerobic and resistance exercises
DIETARY_SUPPLEMENTDietary supplementation4 weeks of preoperative Standard medical therapy which will consist of dietary advice and supplementation

Timeline

Start date
2023-12-15
Primary completion
2024-12-31
Completion
2025-01-31
First posted
2023-12-08
Last updated
2025-08-24

Locations

1 site across 1 country: India

Source: ClinicalTrials.gov record NCT06163001. Inclusion in this directory is not an endorsement.