Clinical Trials Directory

Trials / Recruiting

RecruitingNCT04627376

Multimodal Program for Cancer Related Cachexia Prevention

Effectiveness of a Multimodal Education and Support Program for the Prevention of Cancer Related Cachexia for Patients and Their Family Caregiver

Status
Recruiting
Phase
N/A
Study type
Interventional
Enrollment
60 (estimated)
Sponsor
Cyprus University of Technology · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

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.

Detailed 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.

Conditions

Interventions

TypeNameDescription
OTHERMultimodal education and support program for cancer related cachexia prevention12-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 related to anti cancer treatment.

Timeline

Start date
2020-09-24
Primary completion
2023-02-01
Completion
2026-06-01
First posted
2020-11-13
Last updated
2022-09-02

Locations

1 site across 1 country: Cyprus

Source: ClinicalTrials.gov record NCT04627376. Inclusion in this directory is not an endorsement.