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Routine Evaluation of People Living With Cancer

Routine Evaluation of People Living With Cancer - Body Composition, Physical Function, Systemic Inflammatory Response, Quality of Life and Symptoms

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT04406662
Acronym
REVOLUTION
Enrollment
600
Registered
2020-05-28
Start date
2020-07-15
Completion date
2029-08-08
Last updated
2026-07-07

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Advanced Cancer, Cachexia; Cancer, Quality of Life

Keywords

cancer, advanced cancer, incurable cancer, body composition, physical function, symptoms, cachexia, quality of life, systemic inflammatory response, palliative medicine

Brief summary

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.

Interventions

None listed

Sponsors

University of Edinburgh
Lead SponsorOTHER
NHS Lothian
CollaboratorOTHER_GOV

Study design

Observational model
OTHER
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Patients with incurable cancer (metastatic cancer (Clinical, histological, cytological or radiological evidence) or receiving anti-cancer therapy with palliative intent). * Aged 18-years and over * Written informed consent

Exclusion criteria

* Any concomitant medical or psychiatric problems which, in the opinion of the investigator, would increase the risk of complication for the participant and/or investigator. * Participants will not be able to take part in bio-impedance analysis if they have a pacemaker or implantable cardiac defibrillator.

Design outcomes

Primary

MeasureTime frameDescription
Association between inflammatory cytokines and clinical parameters in incurable cancer2 yearsCorrelation of serum levels of inflammatory cytokines with clinical parameters including skeletal muscle mass, symptom based scores and physical activity as measured by actigraphy.

Countries

United Kingdom

Contacts

CONTACTBarry JA Laird, MBCHB MD
barry.laird@ed.ac.uk01316518611
PRINCIPAL_INVESTIGATORBarry JA Laird, MBCHB MD

St Columba's Hospice/ University of Edinburgh

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Jul 8, 2026