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

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age65+
SponsorBispebjerg Hospital

About this trial

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.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

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.

Disqualifiers

<24 hours admission

Terminal illness in end stage of life

Patients with temporary civil person registration number (CPR)

Trial population

Patients acutely admitted at Bispebjerg Hospital

Trial design

Design model

Cohort

Time perspective

Prospective

Treatments tested in this trial

  • Exposures and measurements

    Other intervention

    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.

Treatment groups

1,500 Participants
are divided into 1 treatment group
Group A: The INSIGHT cohort1 intervention

Trial outcomes

Primary outcomes

1

Length of Hospital Stay

Time (in hours) hospitalized from arrival to discharge

Time frame
From date of hospital admission untill discharge, assessed up to 2 months

Secondary outcomes

1

Readmission

Time to readmission from discharge

Time frame
Time to readmission 30 days from discharge
2

Acute contact

Time to acute contact from discharge

Time frame
Time to acute contact 30 days from discharge
3

Mortality

Time to mortality from index admission

Time frame
Time to mortality 90 days from index admission

Other outcomes

Sponsors and contacts

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