Actively Recruiting

Age: 18Years +
All Genders
Healthy Volunteers
ID06626360

Screening for Malnutrition and Obesity in Patients With COVID-19 and Other Diseases

Led by HAN University of Applied Sciences · Updated on 2024-11-08

2000

Participants Needed

3

Research Sites

17 weeks

Total Duration

On this page

Sponsors

H

HAN University of Applied Sciences

Lead Sponsor

A

Amsterdam University of Applied Sciences

Collaborating Sponsor

AI-Summary

What this Trial Is About

Researchers are investigating how overweight, obesity, and malnutrition influence the outcomes of COVID-19 and other diseases such as cancer. These conditions often occur together and may worsen health results, but the exact mechanisms are not well understood. The study aims to identify key factors linked to worse disease outcomes by reviewing existing literature and analyzing large datasets involving over 150,000 participants. The project includes evaluating the nutritional status and dietary treatments of patients with COVID-19 in primary care. It involves a clinical study to develop a simple screening tool for detecting the coexistence of malnutrition and overweight or obesity in everyday medical practice. The study includes patients who are overweight with a BMI of 25 or higher and are 18 years or older. Participants will be observed and assessed for malnutrition over a nine-month period. Data collection involves reviewing nutritional status and health outcomes related to COVID-19 and cancer. The study also assesses various parameters to understand their impact on disease progression. The findings aim to improve screening and treatment strategies for patients facing both overweight and malnutrition.

CONDITIONS

Brief Title

Screening for Malnutrition in Obese Patients

Who Can Participate

Age: 18Years +
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Age 18 years or older
  • Overweight with a body mass index (BMI) of 25 kg/m8 or higher
Not Eligible

You will not qualify if you...

  • Physically or mentally unable to participate
  • Severe cognitive disorder or severe emotional instability as assessed by a nurse or physician
  • Insufficient proficiency in Dutch to communicate without help
  • Currently residing in a nursing or care home

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Monitoring

Duration - 9 months

Participants with overweight or obesity are observed to evaluate nutritional status and the influence on disease outcomes.

Visits as scheduled by primary care providers

Trial Site Locations

Total: 3 locations

1

OLVG

Amsterdam, Netherlands

Actively Recruiting

2

Ziekenhuis Gelderse Vallei

Ede, Netherlands

Actively Recruiting

3

ErasmusMC

Rotterdam, Netherlands

Actively Recruiting

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Research Team

M

Marian A de van der Schueren, PhD

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

1

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Frequently Asked Questions

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