Screening for Malnutrition in Obese Patients

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18+
SponsorHAN University of Applied Sciences

About this trial

More than half of the Dutch population is overweight or obese, which is associated with an increased risk of COVID-19 and worse outcomes during a COVID-19 infection. In addition, malnutrition and loss of muscle mass are often reported with COVID-19, as well as with cancer and other diseases. Malnutrition and overweight or obesity can coexist, even within the same individual. It is still unclear which mechanisms contribute to the worse outcomes of COVID-19 and other diseases in case of overweight, malnutrition, and a combination of both. The aim of this study is to identify which parameters are associated with worse disease outcomes through literature research and database research (COVID-19 and cancer, more than 150.000 participants). In addition, a clinical study will be conducted aiming to develop a simple screening tool for the recognition of the coexistence of malnutrition and overweight or obesity in clinical practice.

Eligibility criteria

This trial accepts healthy volunteers

Qualifiers

Age 18 years or older

Overweight (BMI of 25 kg/m² or higher)

Disqualifiers

Physically or mentally unable to participate.

Severe cognitive disorder or severe emotional instability, as assessed by the attending nurse or physician.

Insufficient proficiency in the Dutch language to express themselves properly and no interpreter or assistant to help.

Patient resides in a nursing or care home.

Trial population

Hospital in- and outpatients with overweight or obesity

Trial design

Design model

Other

Time perspective

Cross-sectional

Treatments tested in this trial

Not listed

Trial groups

2,000 Participants
are grouped into 1 trial group
Group A: Patients with overweight or obesity

Trial outcomes

Primary outcomes

1

Malnutrition

Malnutrition will be assessed by a working definition based on the GLIM-criteria and a Delphi-study

Time frame
9 months

Secondary outcomes

Other outcomes

Sponsors and contacts

Click on the lead sponsor to view all of their trials.

HAN University of Applied Sciences

Lead sponsor

Amsterdam University of Applied Sciences

Collaborator

National Institute for Public Health and the Environment (RIVM)

Collaborator

Erasmus Medical Center

Collaborator

Wageningen University and Research

Collaborator

Gelderse Vallei Hospital

Collaborator

Amsterdam UMC, location VUmc

Collaborator

Amsterdam UMC, location AMC

Collaborator