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NCT Number: NCT06164925

Standardising and Simplifying the Global Leadership Initiative on Malnutrition (GLIM) for Its More General Application

This observational study of aims to test whether and how the results of GLIM change when using different approaches and methods to carry out its components.

Recruiting

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Observational

Primary location

About this study

The main questions the study aims to answer are:

  • What is the most effective pre-GLIM screening approach?
  • Which of the simple, globally accessible muscle mass measurement methods works the best in the context of GLIM?
  • How does using simpler approaches to screening and muscle mass measurement affect the performance of GLIM in detecting Subjective Global Assessment (SGA) defined malnutrition and 1-year mortality?

Participants will be/have:

  • asked questions about their recent food intake and possible non-volitional weight loss
  • assessed for malnutrition with SGA
  • weighed, and their height will be measured (if not already recorded)
  • their muscle mass measured with a measuring tape (mid-upper arm circumference and calf circumference) and bioelectrical impedance
  • their muscle function measured using hand grip strength
  • have their patient records looked at to extract their weight and height data (if present), diagnoses, routine blood test results, abdominal computed tomography (CT) scan (if present), dual-energy x-ray absorptiometry (DEXA) scan (if present), 1-year mortality and personal identification code for documentation (the latter will be deleted when the study period is over).

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Age of 18+ years
  • Able and willing to sign the consent form
  • Inpatients of the Tartu University Hospital
  • Admitted within 72 hours before enrolment

Exclusion criteria

  • Age of <18 years
  • Inability or refusal to sign the consent form
  • Pregnant or lactating women
  • More than 72 hours passed since admission
  • Patients isolating with an infection

Treatment and study plan

Nutrition screening and assessment

Diagnostic Test

The patient is interviewed for changes in body weight in the last six months and food intake in the last two weeks.

The investigator evaluates the patient's diet, symptoms related to their nutritional status, and functional capacity according to the Subjective Global Assessment (SGA). The SGA tool itself is completed by the researcher.

Height and weight of the patient are measured, if not yet recorded, and BMI is calculated.

The patient's muscle mass is measured using mid-upper arm circumference (MUAC), calf circumference (CC) and bioelectrical impedance (BIA), and their muscle function assessed using hand grip strength.

Primary outcomes

  1. Subjective Global Assessment (SGA) defined malnutrition

    Time frame: baseline, pre-intervention/procedure/surgery

    Subjective Global Assessment (SGA) can be considered a method that is close to a "gold standard" for malnutrition assessment. Therefore, the study will analyse how different approaches to screening and muscle mass measurement affect the performance of GLIM in detecting Subjective Global Assessment (SGA) defined malnutrition.

  2. One-year mortality

    Time frame: through study completion, an average of 1 year

    One year after the data collection, we will look at the patient records to collect the 1-year mortality data. This will give information about whether and how different approaches to components of GLIM affect its ability to predict one-year mortality.

  3. Computed tomography (CT) defined muscle mass

    Time frame: baseline, pre-intervention/procedure/surgery

    One of the GLIM criteria is "reduced muscle mass", and this study will investigate how muscle mass measured with simpler methods compares against muscle mass measured with CT.

  4. DEXA defined muscle mass

    Time frame: baseline, pre-intervention/procedure/surgery

    One of the GLIM criteria is "reduced muscle mass", and this study will investigate how muscle mass measured with simpler methods compares against muscle mass measured with DEXA.

Secondary outcomes

  1. Bioelectrical impedance (BIA) defined muscle mass

    Time frame: baseline, pre-intervention/procedure/surgery

    One of the GLIM criteria is "reduced muscle mass", and this study will investigate how muscle mass measured with simpler methods compares against muscle mass measured with BIA.

Study contacts

Contact information is provided by the study sponsor or research team.

Alastair Forbes, MD

CONTACT

[email protected]

Grete Kurik, BSc

CONTACT

[email protected]

+372 53436535

Sponsors and collaborators

Lead sponsor

University of Tartu

Other

Collaborators

  • Tartu University Hospital

Registry information

Important dates

Study start
2023
Primary completion
2025
Study completion
2025
First posted
Dec 11, 2023
Registry last updated
Mar 28, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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