Skip to content

The Effect of Resistance Training on Muscle Strength and Nutritional Status in Patients With Liver Cirrhosis

The Effect of Resistance Training on Muscle Strength and Nutritional Status in Patients With Liver Cirrhosis

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02343653
Enrollment
39
Registered
2015-01-22
Start date
2015-01-31
Completion date
2018-07-31
Last updated
2017-11-20

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Liver Cirrhosis

Keywords

Malnutrition, Muscle mass, Nutrition

Brief summary

The purpose is to investigate the effect of strength training on muscle strength, muscle mass and nutritional status in patients with liver cirrhosis to clarify possible metabolic and inflammatory changes during this intervention. In addition the investigator examine if the intervention is associated with fewer hospital readmission and an improved quality of life.

Interventions

BEHAVIORALNutrition and strength training

All participants will receive professional dietary guidance and a protein supplement. At the beginning and end of the intervention every participant will be part of a program consisting of: Test of muscle strength, blood samples, assessment of nutritional status, MRi scan, test of Quality of life by questionnaire and test of the ammonium metabolism. After one year readmissions will by registered. The intervention group will receive supervised training.

BEHAVIORALNutrition

All participants will receive professional dietary guidance and a protein supplement. At the beginning and end of the intervention every participant will be part of a program consisting of: Test of muscle strength, blood samples, assessment of nutritional status, MRi scan, test of Quality of life by questionnaire and test of the ammonium metabolism. After one year readmissions will by registered.

Sponsors

Aarhus University Hospital
CollaboratorOTHER
University of Aarhus
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Cirrhosis, Child Pugh score A and B

Exclusion criteria

* Cirrhosis, Child-Pugh score C at inclusion * Neurological and/or psychiatric disorder * Pregnancy, breastfeeding * Patients with malignancy * Patients with hepatic encephalopathy at inclusion * Patients with atypical diets, such as vegans

Design outcomes

Primary

MeasureTime frame
Maximal voluntary muscle strength in knee extensor will be measured by an isokinetic dynamometer and hand strength by hand dynamometer.12-14 weeks

Secondary

MeasureTime frameDescription
Readmissions as measured by a follow-up one year after the intervention.1-1,5 year
Quality of Life as measured by a standardized questionnaire (SF-36)12-14 weeks
Nutritional status as measured by Triceps skinfold thickness (TSF), mid-upper-arm circumference (MUAC), mid-arm muscle area (MAMA) and hand dynamometer12-14 weeks
Ammonia metabolism as measured by Oral Glutamine Challenge Test12-14 weeksMinimal risk in the taking of blood samples. The participant can experience nausea and dizziness but will not be left unsupervised during the test.
Muscle mass as measured by MRi scan and bioimpedance scan.12-14weeks
Insulin sensitivity as measured by HOMA-IR12-14 weeks

Countries

Denmark

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 2, 2026