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Completed

NCT Number: NCT06163001

Role of Exercise in Chronic Liver Disease Patients Undergoing Liver Transplantation

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.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Institute of Liver and Biliary Sciences

New Delhi, National Capital Territory of Delhi, 110070, India

About this study

  • 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).

  • 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.
  • 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.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

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

Exclusion criteria

  • Patients with a physical disability (upper or lower limb deformity/abnormality)
  • Exercise intolerance or inability to follow exercise regime.
  • Patients who fail the screening tests.
  • 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.

Treatment and study plan

Supervised aerobic and resistance exercises

Behavioral

4 weeks of preoperative supervised aerobic and resistance exercises

Other names: physiotherapy, exercise therapy

Dietary supplementation

Dietary Supplement

4 weeks of preoperative Standard medical therapy which will consist of dietary advice and supplementation

Primary outcomes

  1. Liver frailty index

    Time frame: 4 weeks post intervention, Post op day 14, Post op day 30

    Robust defined as LFI <3.2, prefrail defined as LFI between 3.2 and 4.4, and frail defined as LFI ≥4.5

  2. short physical performance battery

    Time frame: 4 weeks post intervention, Post op day 14, Post op day 30

    SPPB scores range from zero to 12 possible points. SPPB score of 3-9 points in persons with possible sarcopenia but no mobility disability indicates frailty; SPPB score of 10 or greater for persons with no sarcopenia and no mobility disability indicates robustness

  3. pulmonary function test

    Time frame: 4 weeks post intervention, Post op day 14, Post op day 30

    PEF would be tested

  4. pulmonary function test

    Time frame: 4 weeks post intervention, Post op day 14, Post op day 30

    FEV1 would be tested

Secondary outcomes

  1. Time to extubation

    Time frame: Till Post op day 90

  2. Need for re-intubation

    Time frame: Till Post op day 90

  3. Duration of NIV support

    Time frame: Till Post op day 90

  4. Mortality

    Time frame: 90 days

  5. Myostatin levels in blood

    Time frame: Post intervention at 4 weeks & on Post op day 14

  6. Skeletal muscle mass- L3 Skeletal Muscle Index

    Time frame: Post intervention at 4 weeks & on Post op day 14

  7. Time to mobilization out of bed

    Time frame: Till Post op day 90

  8. Length (Days) of ICU stay

    Time frame: Till Post op day 90

  9. Number of days of hospital stay

    Time frame: Till Post op day 90

  10. Incidence of all septic complications

    Time frame: Till Post op day 90

  11. Major surgical complications (CDC > grade 3)

    Time frame: Till Post op day 90

  12. Pulmonary complications- Clinical evaluation

    Time frame: Till Post op day 90

Sponsors and collaborators

Lead sponsor

Institute of Liver and Biliary Sciences, India

Other

Registry information

Official study title

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

Important dates

Study start
2023
Primary completion
2024
Study completion
2025
First posted
Dec 8, 2023
Registry last updated
Aug 24, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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