Multimodal Program for Cancer Related Cachexia Prevention

Status Recruiting

Clinical Trial Summary

The aim of the study is to evaluate the effectiveness of a multifactorial education and support program for the prevention of cancer-related cachexia syndrome, for patients and their family caregivers during anti-cancer treatment.

Clinical Trial Description

After being informed about the study and the need to nominate a family caregiver, all patients and their family caregiver giving written informed consent, they will undergo a 12-weeks multimodal program. Randomly they will divided into two groups (intervention and control). This 12-weeks multimodal program includes 4 meetings (with cancer nurse and clinical dietician). In this 4 meetings (about 30 minutes) they will have blood tests (CRP, Albumin levels), body composition measurements, questionnaires, education on their diet and symptom management. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT04627376
Study type	Interventional
Source	Cyprus University of Technology
Contact	Andreas Charalambous, PhD
Phone	00357-25002011
Email	andreas.charalambous@cut.ac.cy
Status	Recruiting
Phase	N/A
Start date	September 24, 2020
Completion date	June 2026

View Details

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