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Recruiting NCT07169526

Health Literacy and Self-efficacy Expectations in Patients With Alcohol-related Liver Cirrhosis

Observational Self-Efficacy Health Literacy Liver Cirrhosis ALD - Alcoholic Liver Disease

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
This is an observational study: the protocol does not assign a study treatment.
Who it may be relevant to
Registry conditions: Self-Efficacy, Health Literacy, Liver Cirrhosis, ALD - Alcoholic Liver Disease. Basic parameters: 18 years — 99 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
Germany
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Official title

Gesundheitskompetenz Und Selbstwirksamkeitserwartung Bei PatientInnen Mit Alkoholbedingter Leberzirrhose

Overview

The goal of this observational study is to quantify the health literacy and self-efficacy in people with alcohol-related liver cirrhosis.

Primary outcome measures

  • Level of self-efficacy at baseline, assessed using the Scale for General Self-Efficacy (Skala zur Allgemeinen Selbstwirksamkeitserwartung) [Time frame: baseline]
  • Level of health literacy at baseline, assessed using the European Health Literacy Survey Questionnaire (HLS-EU-Q47) [Time frame: baseline]
Secondary outcome measures (4)
  • Occurrence of hepatic decompensation or liver-related death [Time frame: until end of study]
  • Rehospitalization due to liver-related complications [Time frame: Throughout study completion (up to 12 months)]
  • Hepatic decompensation episodes [Time frame: Throughout study completion (up to 12 months)]
  • Level of quality of life, assessed using the [e.g., SF-36 Questionnaire] [Time frame: baseline]

Eligibility criteria

Inclusion criteria

  • age (18-99)
  • liver cirrhosis

Exclusion criteria

  • pregnancy
  • insufficient german

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: Yes

Study design

Observational model
Cohort

Study locations

Germany · 1 center
  • Medizinische Hochschule Hannover — Hanover

Identifiers

NCT: NCT07169526 · 12014-BO-K-2025 · 12014-BO-K-2025

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗