Multimodal Program for Cancer Related Cachexia Prevention (NCT04627376) | Clinical Trial Compass
RecruitingNot Applicable
Multimodal Program for Cancer Related Cachexia Prevention
Cyprus60 participantsStarted 2020-09-24
Plain-language 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.
Who can participate
Age range
18 Years
Sex
ALL
See this in plain English?
AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Inclusion criteria
. 18 years old or older
. Participants must be diagnosed with solid tumour (stomach, colorectal, pancreas, breast, lung)
. Participants must be normal or pre cachectic as defined by the guidelines
. Read and understand Greek or English
Exclusion criteria
. Haematologic tumors
. Parenteral Nutrition
. ECOG Performance status \>2 or Karnofsky Performance Status \<60%
. Participant who can not introduce a family caregiver
. Participants in cachexia or refractory cachexia stage as defined by the guidelines below:
. Patients who use complementary therapies (ex-acupuncture)
Questions worth asking your doctor
Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.
1Based on my diagnosis and history, is this trial worth exploring for me — or is there a standard treatment we should try first?
2What does this trial's phase tell us about how much is already known about its safety and benefit?
3What would taking part actually involve for me — visits, tests, time, and travel?
4What are the known and possible risks or side effects I should weigh, and how would they be monitored?
5If this trial isn't the right fit, what other options or trials would you suggest I look into?
Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.
Questions for the trial coordinator
The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.
1What does taking part actually involve week to week — how many visits, where, and how long does each one take?
2What costs are covered by the study, and what might I have to pay for myself, including travel, parking, or time off work?
3What happens during screening, and what happens if the study team confirms I don't meet the criteria after those tests?
4Who pays for the scans, blood work, and other tests the trial requires — the study, my insurance, or me?
5How will being in the trial affect my regular care, and will my own doctor stay informed and involved?
6Can I leave the trial at any point if I change my mind, and what would happen to my care if I do?
A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.
What they're measuring
1
Change from baseline in pre-cachexia stage against cachexia criteria at 12 weeks