Actively Recruiting

Age: 18Years - 100Years
All Genders
ID04502719

Comparison of Two Nutritional Screening Tools for the Detection of Malnutrition in Patients with Liver Cirrhosis

Led by Hospital Clinic of Barcelona · Updated on 2024-12-03

46

Participants Needed

1

Research Sites

26 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Researchers are evaluating two nutritional screening questionnaires, the Royal Free Hospital Nutritional Prioritizing Tool (RFH-NPT) and the Liver Disease Undernutrition Screening Tool (LDUST), in patients with liver cirrhosis. The study aims to compare how well these tools detect the risk of malnutrition in cirrhotic patients, a group for whom traditional screening methods have limitations due to disease-related changes like ascites. The study also looks at the prevalence of sarcopenia and its impact on patients' quality of life. Participants will be screened using both RFH-NPT and LDUST questionnaires, followed by a complete nutritional assessment based on new diagnostic criteria promoted by the Global Leadership Initiative on Malnutrition. Additionally, sarcopenia risk will be assessed using the SARC-F questionnaire, and quality of life will be measured with the Chronic Liver Disease Questionnaire. All assessments occur within 48 hours for primary and secondary outcomes, with adverse clinical outcomes monitored over 6 months. During the study, patients will undergo detailed nutritional and sarcopenia assessments along with quality of life questionnaires. Researchers will track malnutrition diagnosis agreement between tools, prevalence of malnutrition and sarcopenia, quality of life scores, and any adverse clinical events over six months. This observational study does not involve assigned treatments but focuses on validating screening tools to better detect malnutrition risk in liver cirrhosis patients.

CONDITIONS

Brief Title

Comparison of Nutritional Screening Tools in Liver Cirrhosis Patients

Who Can Participate

Age: 18Years - 100Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Patients diagnosed with liver cirrhosis
Not Eligible

You will not qualify if you...

  • Patients with cognitive impairment or major psychiatric disorder
  • Lack of consent from the patient for inclusion in the study
  • Any patient who is not suitable based on the researcher's own judgement

AI-Screening

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Diagnostic Evaluation

Duration - 48 hours

Participants complete nutritional screening questionnaires to assess malnutrition risk and related health factors.

1 visit (in-person)

Long-term Monitoring

Duration - 6 months

Participants are observed for adverse clinical outcomes and quality of life over time.

Follow-up visits as scheduled

Trial Site Locations

Total: 1 location

1

Hospital Clinic de Barcelona

Barcelona, Catalonia, Spain, 08036

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Research Team

J

Joan Trabal, RDN, PhD

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

1

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