Actively Recruiting
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
Eligibility Criteria
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
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
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
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
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
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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