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NCT06310993Not yet recruiting

Exercise to Boost Immunity in Advanced Cancer

Exercise to Boost Immunity in Advanced Cancer: Feasibility of Combined Aerobic Exercise and Resistance Training for Patients with Advanced Mesothelioma and Pancreatic Cancer

Source: ClinicalTrials.gov · Last updated 3 Dec 2024 · Not updated for over 12 months - ask the site whether it is still open

Brief summary (registry, in English)

The trial is a prospective feasibility trial conducted in Sheffield. Recruitment will include twenty patients receiving first line palliative immunotherapy for advanced, unresectable or metastatic mesothelioma and patients receiving first line systemic anti-cancer treatment for pancreatic cancer. Patients will attend the AWRC for a supervised exercise session once a week to include aerobic exercise along with an unsupervised weekly exercise session for 3 months. Blood samples will be collected at baseline and then monthly for 3 months, pre and post the supervised exercise session. Cytokine, myokine and immune cell concentration will be analysed using cytokine bead-based multiplex immune assays and RNA-seq to full profile changes in gene and protein expression

Status (registry)
Not yet recruiting
Study type
Interventional
Enrollment
30 (estimated)
First submitted
28 Feb 2024
Start date
1 Sept 2025
Primary completion date
1 Mar 2027
Lead sponsor
Sheffield Teaching Hospitals NHS Foundation Trust
NCT number
NCT06310993

What you commit to

  • Study type: Interventional
  • Planned participants: 30
  • From 1 Sept 2025 to the primary completion date, 1 Mar 2027
  • 2 sites in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Prior treatment with systemic anti-cancer treatment
  • Patients who have progressed on first line palliative immunotherapy for advanced, unresectable, or metastatic mesothelioma.

Other illness

  • More than one primary cancer
  • Patients who have progressed on first line palliative chemotherapy for advanced, unresectable, or metastatic pancreatic cancer.
  • No histological or cytological diagnosis of mesothelioma or pancreatic cancer.

Age

  • Age below 18 years old

Other

  • Uncontrolled brain or bone metastases
  • Patients with active co-morbidities that would prevent or limit their participation in the exercise intervention
  • ECOG Performance status of 2 or more
  • Unable to provide informed consent

Who the study is looking for

  • Patients about to start or who are undergoing first line palliative immunotherapy for advanced, unresectable, or metastatic mesothelioma or patients about to start or who are undergoing first line palliative chemotherapy for advanced, unresectable, or metastatic pancreatic cancer.
  • Age over 18 years old
  • Histological or cytological diagnosis of mesothelioma or pancreatic cancer.
  • ECOG Performance status 0-1 (to be assessed by clinician)
  • Ability to provide informed consent

Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (2)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Sheffield Hallam University
Coordinator of this site? Confirm its status
SheffieldUnited KingdomUnknown status
Cancer Research Centre at Weston Park Hospital
Coordinator of this site? Confirm its status
SheffieldUnited KingdomUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.