Investigation of the Relationship Between Nutritional Status Assessment and Frailty in Critical Care Patients

NCT07143084 · tracked via the Priya Life Science Turkey tracker

Sponsor

Ankara Training and Research Hospital

Phase

Observational

Started

2025-05-15

Last updated

2026-03-19

Condition(s) studied

FrailityCritical Illness

Study summary

This study aims to understand the effects of these two parameters on clinical outcomes by examining the relationship between NUTRIC and CONUT scores in intensive care patients. The results of the study may contribute to the development of new approaches to the treatment process of patients by better understanding the relationship between nutritional status and pre-hospital frailty in intensive care units. In addition, eliminating the deficiencies in this area will pave the way for the creation of more effective and personalized treatment plans for similar patients.

Eligibility

Sex

ALL

Min age

65 Years

Max age

—

Healthy volunteers

Inclusion Criteria: * over 65 * 48 hours min. ICU stay Exclusion Criteria: * Patients who are under 65 years of age * whose intensive care stay does not exceed 48 hours * who have missing data for serum albumin or lymphocyte count or total cholesterol, * who have been diagnosed with hematological diseases such as leukemia or lymphoma

Primary outcome measure(s)

Correlation between CONUT scale and frailty in intensive care patients — From enrollment 2 days
To evaluate the correlation between the CONUT scale and frailty, Pearson or Spearman correlation analysis will be performed depending on suitability for normal distribution. Logistic regression analysis will be performed to assess the independent association between CONUT scale and frailty. Potential confounding variables such as age, gender, APACHE II score, and activities of daily living will be included in the regression model.

Trial sites (1)

Facility	City	Region	Status
Ankara Training And Research Hospital	Altındağ	Ankara

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Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07143084 on ClinicalTrials.gov ↗ ← All trials in Turkey