Clinical Trials Directory

Trials / Terminated

TerminatedNCT03266575

Pulmonary Rehabilitation in End-Stage Liver Disease

Does Pulmonary Rehabilitation Improve Frailty and Sarcopenia in End Stage Liver Disease?

Status
Terminated
Phase
N/A
Study type
Interventional
Enrollment
4 (actual)
Sponsor
Mayo Clinic · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

The purpose of this study is to assess the impact of exercise on sarcopenia and frailty. The exercise that will be performed in this study will include either pulmonary rehabilitation or a formal home based video strengthening program

Detailed description

Participants will be randomized into two groups. The Pulmonary Rehabilitation group will undergo exercise under a supervised setting for a total duration of 12 weeks. Patients will perform endurance (treadmill or cycle ergometer), strength (weight resistance) and flexibility training twice a week for a period of an hour per session. Exercises will be supervised by physiotherapists or exercise physiologists. Compliance and performance will be monitored by the trainer. They will receive a pedometer for home use. The Home based program group will perform REST for 10 minutes daily, increasing to 20 minutes daily, after the second week, in their home environment. The total duration of the intervention will be 12 weeks. Patients will be provided with pedometers, REST video and binder, with instructions on how to perform exercises, and resistance bands.

Conditions

Interventions

TypeNameDescription
BEHAVIORALPulmonary Rehabilitation ExerciseParticipants will undergo Pulmonary Rehabilitation exercise. Participants will perform endurance (treadmill or cycle ergometer), strength (weight resistance) and flexibility training twice a week for a period of an hour per session
BEHAVIORALHome Based ExerciseParticipants will undergo Home based exercise program consisting of strength and conditioning. Participants will perform REST for 10 minutes daily, increasing to 20 minutes daily, after the second week, in their home environment. The total duration of the intervention will be 12 weeks. Participants will be provided with pedometers, REST video and binder, with instructions on how to perform exercises, and resistance bands.

Timeline

Start date
2018-02-01
Primary completion
2024-12-09
Completion
2024-12-09
First posted
2017-08-30
Last updated
2024-12-12

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT03266575. Inclusion in this directory is not an endorsement.