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Recruiting NCT06946537

Nutritional Status and Patient Characteristics Upon Length of Stay, Clinical Outcome, and Survival in Older Hospitalized Patients

Observational Geriatric Malnutrition Length of Stay

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
The protocol lists: Exposures and measurements.
Who it may be relevant to
Registry conditions: Geriatric, Malnutrition, Length of Stay. Basic parameters: from 65 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
Denmark
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

The Influence of Nutritional Status and Phenotypic Characteristics Upon Length of Stay, Clinical Outcome, and Survival in Hospitalized Patients

Overview

Disease-related malnutrition (DRM) describes undernutrition or imbalances in energy, protein, or other nutrient-needs, caused by a concomitant disease. Nutritional status plays a vital role in the fate of hospitalized patients, and DRM is associated with loss of function and decreased survival. DRM is a common condition in patients with acute illnesses, approximately 30% among medical inpatients are malnourished when admitteed to the hospital, and rise higher among the older or critically ill. Physiologically malnutrition is associated with a) poorer tissue healing and restitution after severe disease, b) suppressed immune function and resistance towards infections, c) poorer metabolic defense towards critical disease, d) delayed and poorer progress of chronic diseases. In addition, inadequate nutrition is coupled to a prolonged hospital stay, resulting in more readmissions, and overall higher mortality in hospital patients. Yet, nutritional status of patients upon hospital admittance is seldom systematically assessed and the consequences of DRM in older acutely admitted patients still needs to be understood. This project will provide a detailed description of nutritional, physiolgical, and biochemical status of 1500 acutely admitted patients. In relation, the study will investigate the relation between patient characteristics and disease progression. The obtained data will also be coupled to patient registers to investigate the link between length of hospital stay, readmissions and acute contact, and mortality.

Interventions

  • Other Exposures and measurements
    Anthropometry, Body composition (BIA), Nutritional screening (GLIM, SNAQ, NIS, NRS-2002), Functional tests, Seisomocardiography, Muscle strength, Blood tests, Fecal swabs, Indirect calorimetry Orientation-Memory-Concentration (OMC), Sarcopenia, Frailty (Clinical Frailty Scale), Comobidity, Polypharmacy, Portrait photo.

Primary outcome measures

  • Length of Hospital Stay [Time frame: From date of hospital admission untill discharge, assessed up to 2 months]
Secondary outcome measures (3)
  • Readmission [Time frame: Time to readmission 30 days from discharge]
  • Acute contact [Time frame: Time to acute contact 30 days from discharge]
  • Mortality [Time frame: Time to mortality 90 days from index admission]

Eligibility criteria

Inclusion criteria

  • Acutely admitted adults aged 65 years and above.
  • Be able to comply with the study information, as assessed by the research personnel.
  • Be able to understand Danish.

Exclusion criteria

  • <24 hours admission
  • Terminal illness in end stage of life
  • Patients with temporary civil person registration number (CPR)

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

Healthy volunteers: No

Study design

Observational model
Cohort

Study locations

Denmark · 1 center
  • Bispebjerg Hospital — Copenhagen

Identifiers

NCT: NCT06946537 · H-25009586

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗