Role of Exercise in Chronic Liver Disease Patients Undergoing Liver Transplantation

Institute of Liver and Biliary Sciences, India

Status: Completed

Conditions: Chronic Liver Disease and Cirrhosis; Frailty

Treatments: Dietary Supplement: Dietary supplementation; Behavioral: Supervised aerobic and resistance exercises

Study type: Interventional

Funder types: Other

Identifiers

NCT06163001

ILBS-LDLT-02

Details and patient eligibility

About

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.

Full 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.

Enrollment: 60 patients

Sex: All

Ages: 18+ years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• Voluntary adult patient (>18 years), decompensated chronic liver disease patients planned for LDLT, and Who pass the screening tests done in the OPD

  1. Able to follow the introductory level exercises as per the protocol in the OPD without any adverse event.
  2. No drop in the spO2 less than 93% on a 6 minute walk test.

Exclusion criteria

1. Patients with a physical disability (upper or lower limb deformity/abnormality)

2. Exercise intolerance or inability to follow exercise regime.

3. Patients who fail the screening tests.

4. Patients on the following drugs-

   • Higher corticosteroid dose (>0.1mg/kg/day),
   • BCAA (Branched chain amino acids)
   • Growth hormone, testosterone, SARMs,
   • Ghrelin agonists, myostatin antibodies,
   • Activin IIR antagonists, angiotensin converting enzyme inhibitors,
   • Espindolol (mixed beta agonist and antagonists), and
   • Fast skeletal muscle troponin activators.

Trial design

Primary purpose: Supportive Care

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: None (Open label)

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60 participants in 2 patient groups

Exercise Group

Experimental group

Treatment:

Behavioral: Supervised aerobic and resistance exercises

Dietary Supplement: Dietary supplementation

Dietary supplementation

Active Comparator group

Treatment:

Dietary Supplement: Dietary supplementation