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Clinical Trials/NCT06606184
NCT06606184
Completed
N/A

Benefits of Pulmonary Rehabilitation to Patients Post Liver Transplant

Chang Gung University1 site in 1 country78 target enrollmentJanuary 1, 2022

Overview

Phase
N/A
Intervention
Not specified
Conditions
Liver Transplant Surgery
Sponsor
Chang Gung University
Enrollment
78
Locations
1
Primary Endpoint
Respiratory Muscle Stregnth Test
Status
Completed
Last Updated
last year

Overview

Brief Summary

The goal of this clinical trial was to access the benefits of a 12-week home-based pulmonary rehabilitation regimen on pulmonary function recovery in post-liver transplant patients. The main questions it aims to answer are:

Does pulmonary rehabilitation facilitate pulmonary muscle strength recovery? Does the intervention improve pulmonary function and reduce dyspnea sensation?

Participants performed:

Inspiratory muscle training twice a day for 12 weeks after discharged from the hospital Upper limb resistive training Lower limb exercise

Detailed Description

Patients undergoing liver transplantation often face significant challenges related to pulmonary rehabilitation. Although postoperative rehabilitation has been extensively studied, the specific role of pulmonary rehabilitation programs has received limited attention. This study aims to evaluate the efficacy of a home-based pulmonary rehabilitation program in improving respiratory function recovery among post-liver transplant patients. The training group participated in a 12-week pulmonary rehabilitation program post-discharge, emphasizing respiratory muscle and exercise training, while the control group received standard care, which included traditional rehabilitation.

Registry
clinicaltrials.gov
Start Date
January 1, 2022
End Date
December 31, 2023
Last Updated
last year
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Hui-Ling Lin

Professor

Chang Gung University

Eligibility Criteria

Inclusion Criteria

  • Age 20 years or older
  • Scheduled to undergo living donor liver transplantation
  • Stable vital signs
  • Normal cognitive function
  • Able to perform activities independently using their own strength and coordination
  • Willing and able to participate in 12 weeks of rehabilitation training

Exclusion Criteria

  • Severe physical illness during the operation
  • Acute bleeding
  • Unstable vital signs
  • Hepatic encephalopathy, or neurological conditions such as stroke, Parkinson\'s disease, or cognitive dysfunction
  • Limited mobility (e.g., unable to stand, lift upper limbs, or bedridden)
  • Inability to comply with 12 weeks of pulmonary rehabilitation post-discharge
  • Unstable vital signs
  • Hepatoencephalopathy, such as cardiovascular accident, Parkinson disease, cognitive dysfunction
  • Those with limited mobility (unable to stand, unable to lift upper limbs, or bedridden)
  • Those who are unable to cooperate with the 12 weeks of pulmonary rehabilitation exercises after discharge.

Outcomes

Primary Outcomes

Respiratory Muscle Stregnth Test

Time Frame: Throughout the study completion, approximately 3 month

Respiratory muscle strength was determined by Maximum Inspiratory Pressure (MIP) using a pressure monometer.

Secondary Outcomes

  • Oxygenation status(Participants underwent maximum inspiratory and expiratory pressure measurements at four time points: upon admission, before discharge from the intensive care unit, before discharge from the hospital, and at the end of the 12-week enrollment period.)
  • Dyspnea Severity Assessment(Throughout the study completion, approximately 3 month)
  • Forced Vital Capacity(Throughout the study completion, approximately 3 month)

Study Sites (1)

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