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
| Type | Name | Description |
|---|---|---|
| OTHER | Multimodal education and support program for cancer related cachexia prevention | 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 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.