Actively Recruiting

Age: 18Years +
All Genders
ID06499623

Early Detection of Malnutrition in Oncology Patients and People Over 65 Years of Age

Led by Institute of Health Information and Statistics of the Czech Republic · Updated on 2024-10-03

2000

Participants Needed

9

Research Sites

17 weeks

Total Duration

On this page

Sponsors

I

Institute of Health Information and Statistics of the Czech Republic

Lead Sponsor

B

Brno University Hospital

Collaborating Sponsor

AI-Summary

What this Trial Is About

Researchers are conducting a national, prospective, multicenter observational study in the Czech Republic to evaluate early detection methods for malnutrition in oncology patients and hospitalized patients aged 65 years and older. The goal is to develop a standardized diagnostic process that improves quality of life and treatment effectiveness by enabling timely nutritional interventions for these patient groups. This pilot project will include about 1,500 oncology patients and 500 elderly patients. The study involves assessing participants using diagnostic tests such as blood tests measuring albumin, C-reactive protein, cholesterol, urea, creatinine, and vitamin D levels, as well as bioelectrical impedance analysis to evaluate body composition. Participants will also complete a nutritional risk assessment questionnaire focusing on weight loss, BMI, food tolerance, and cancer diagnosis with ongoing treatment. The project aims to establish a unified standard for nursing practice to identify malnutrition early and start appropriate nutritional support. Participants will be monitored through these assessments until March 31, 2026. Researchers will track the number of patients identified with malnutrition using the PSNPO questionnaire and the proportion who receive nutritional interventions. The study is supported by national and European funding, with the goal of improving care standards for oncology and elderly hospitalized patients by better managing malnutrition risks.

CONDITIONS

Brief Title

Early Detection of Malnutrition in Oncology Patients and Elderly Patients

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • For oncology patients: age 18 or older, diagnosed with cancer, and survival prognosis of at least 3 months
  • For patients aged 65 and older: hospitalized for at least 14 days or longer
Not Eligible

You will not qualify if you...

  • Not agreeing to participate in the project

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)

Diagnostic Evaluation

Duration - Up to 3 years

Participants undergo diagnostic tests including blood tests, bioelectrical impedance analysis, and nutritional risk assessment questionnaires to detect malnutrition.

Visits as needed for diagnostic testing during hospitalization or oncology treatment

Long-term Monitoring

Duration - Up to 3 years

Participants are monitored over time to observe nutritional status and the initiation of nutritional interventions if necessary.

Ongoing assessments during hospital stay for patients 65 and older and during oncology treatment for oncological patients

Trial Site Locations

Total: 9 locations

1

Brno University Hospital

Brno, Czechia, 60200

Enrolling by Invitation

2

Masaryk Memorial Cancer Institute

Brno, Czechia, 60200

Actively Recruiting

3

Hospital AGEL Nový Jičín a.s.

Nový Jičín, Czechia

Actively Recruiting

4

University Hospital Olomouc

Olomouc, Czechia

Enrolling by Invitation

5

University Hospital Pilsen

Pilsen, Czechia

Enrolling by Invitation

6

Bulovka Hospital

Prague, Czechia

Actively Recruiting

7

General University Hospital, Prague

Prague, Czechia

Enrolling by Invitation

8

Military University Hospital, Prague

Prague, Czechia

Actively Recruiting

9

University Hospital, Motol

Prague, Czechia

Actively Recruiting

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Research Team

N

Nikola Stourac

L

Lucie Mandelova, 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

2

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