Institute of Liver and Biliary Sciences
New Delhi, National Capital Territory of Delhi, 110070, India
NCT Number: NCT06163001
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.
Looking for future studies?
Notify Me18 year and older
All sexes
Interventional
Not applicable
New Delhi, National Capital Territory of Delhi, 110070, India
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).
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
4 weeks of preoperative supervised aerobic and resistance exercises
Other names: physiotherapy, exercise therapy
4 weeks of preoperative Standard medical therapy which will consist of dietary advice and supplementation
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
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
Time frame: 4 weeks post intervention, Post op day 14, Post op day 30
PEF would be tested
Time frame: 4 weeks post intervention, Post op day 14, Post op day 30
FEV1 would be tested
Time frame: Till Post op day 90
Time frame: Till Post op day 90
Time frame: Till Post op day 90
Time frame: 90 days
Time frame: Post intervention at 4 weeks & on Post op day 14
Time frame: Post intervention at 4 weeks & on Post op day 14
Time frame: Till Post op day 90
Time frame: Till Post op day 90
Time frame: Till Post op day 90
Time frame: Till Post op day 90
Time frame: Till Post op day 90
Time frame: Till Post op day 90
Institute of Liver and Biliary Sciences, India
Other
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
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.
Published trials that share one or more normalized conditions with this study.
NCT06892366
Atrophy, Behavior
Ankara, Altındağ, Turkey (Türkiye)
View Trial DetailsNCT06827769
Chronic Liver Disease and Cirrhosis, Fibrosis
Tanta, Gharbyea, Egypt
View Trial DetailsNCT05717569
Chronic Liver Disease and Cirrhosis, Fibrosis
Cairo, Egypt
View Trial DetailsNCT05407272
Acute Kidney Injury, Alzheimer Disease
Yilan, Taiwan
View Trial Details