Actively Recruiting
Routine Evaluation of People Living With Cancer
Led by University of Edinburgh · Updated on 2025-07-03
600
Participants Needed
1
Research Sites
473 weeks
Total Duration
On this page
Sponsors
U
University of Edinburgh
Lead Sponsor
N
NHS Lothian
Collaborating Sponsor
AI-Summary
What this Trial Is About
People with incurable cancer often have complex individual needs, however there are several common themes encountered when considering this group. As cancer progresses there are series of interactions between the tumour and the patient, producing both local and systemic effects. This altered state of illness can have multiple ill effects including weight loss, fatigue, increased symptom burden and reduction in physical function which all contribute to a reduced quality of life. These areas are often studied in isolation, giving an incomplete picture. A detailed, holistic characterisation of this group of people does not exist. A robust characterisation of people with incurable cancer will allow identification and prioritisation of future research and has the potential to inform new therapeutics and provide justification for treatments. This study aims to collect information about symptoms and quality of life, weight loss and body composition, physical activity and the body's immune response to cancer. Participants with incurable cancer will be recruited to the study from oncology and palliative medicine services in the UK. Participants will answer questionnaires about quality of life and symptoms, have bloods taken for inflammatory marker and cytokine analysis and have their body composition measured by a variety of methods.
CONDITIONS
Official Title
Routine Evaluation of People Living With Cancer
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Patients with incurable cancer (metastatic cancer confirmed by clinical, histological, cytological, or radiological evidence) or receiving anti-cancer therapy with palliative intent
- Age 18 years or older
- Provided written informed consent
You will not qualify if you...
- Any medical or psychiatric condition that could increase risk for the participant or investigator, as judged by the investigator
- Inability to participate in bio-impedance analysis due to having a pacemaker or implantable cardiac defibrillator
AI-Screening
AI-Powered Screening
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Trial Site Locations
Total: 1 location
1
St Columba's Hospice
Edinburgh, United Kingdom, EH53RW
Actively Recruiting
Research Team
B
Barry JA Laird, MBCHB MD
CONTACT
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
0
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