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Trial Title:
Nutrition Childhood Cancer Survivors
NCT ID:
NCT05481229
Condition:
Childhood Cancer
Nutrition Disorders
Conditions: Official terms:
Nutrition Disorders
Conditions: Keywords:
children cancer survivors
adiposity
late effects
nutriton
adipokines
Study type:
Observational
Overall status:
Unknown status
Study design:
Time perspective:
Prospective
Intervention:
Intervention type:
Other
Intervention name:
nutritional interventions
Description:
Nutritional intervention will be initiated in patients at risk of overweight and obesity.
A targeted nutritional intervention will be carried out, which will include consultation
on dietary habits and physical activity as determined by diet and physical activity
records. Consultations will be aimed at improving lifestyle and maintaining an adequate
body weight.
Summary:
NUTRITION CCS is a cross-sectional, descriptive study to assess the relationship between
body composition and demographic, socioeconomic status, treatment modalities and blood
samples of survivors who were in remission. The study was conducted in the Clinic for
childhood cancer survivors. The clinic is attended by patients older than 18 years and
was built in 2016 at the St. Anne's Hospital in Brno.
Detailed description:
NUTRITION CCS is a cross-sectional, descriptive study to assess the relationship between
body composition and demographic, socioeconomic status, treatment modalities and blood
samples of survivors who were in remission.
Objectives of the study
1. to determine the prevalence (incidence) of nutritional disorders, especially obesity
and metabolic syndrome, in cured paediatric cancer patients in adulthood;
2. to investigate the role of adipokines in the development of cardiometabolic
complications in this group of patients; 3. to determine whether targeted dietary
and lifestyle interventions can lead to improvements in nutritional status and
subjectively perceived quality of life of treated paediatric cancer patients in
adulthood and objectively assessed cardiometabolic risk
Criteria for eligibility:
Study pop:
The study population is patients who have been treated for childhood or adolescent cancer
and who are now being followed up in a dispensary clinic.
Sampling method:
Probability Sample
Criteria:
Inclusion Criteria:
- Patients after treatment from childhood and adolescent cancers.
- The subject is male or female, aged 18 - 64 years
Exclusion Criteria:
- Patients with acute cancer therapy
- Pregnant women
Gender:
All
Minimum age:
18 Years
Maximum age:
64 Years
Healthy volunteers:
No
Locations:
Facility:
Name:
Masaryk University
Address:
City:
Brno
Zip:
625 00
Country:
Czechia
Status:
Recruiting
Contact:
Last name:
Julie Bienertová-Vašků, Prof.
Investigator:
Last name:
Lucie Štrublová, Mgr.
Email:
Sub-Investigator
Investigator:
Last name:
Jan Kučera, Ph.D.
Email:
Sub-Investigator
Facility:
Name:
St. Anne Hospital in Brno
Address:
City:
Brno
Zip:
656 91
Country:
Czechia
Status:
Recruiting
Contact:
Last name:
Tomáš Kepák, MUDr.
Email:
tomas.kepak@fnusa.cz
Investigator:
Last name:
Lucie Štrublová, Mgr.
Email:
Sub-Investigator
Investigator:
Last name:
Viera Bajčiová, MUDr.
Email:
Sub-Investigator
Investigator:
Last name:
Hana Hrstková, Prof.
Email:
Sub-Investigator
Investigator:
Last name:
Jaroslav Štěrba, Prof.
Email:
Sub-Investigator
Start date:
April 25, 2018
Completion date:
April 25, 2023
Lead sponsor:
Agency:
Masaryk University
Agency class:
Other
Collaborator:
Agency:
St. Anne's University Hospital Brno, Czech Republic
Agency class:
Other
Source:
Masaryk University
Record processing date:
ClinicalTrials.gov processed this data on November 12, 2024
Source: ClinicalTrials.gov page:
https://clinicaltrials.gov/ct2/show/NCT05481229
