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UNKNOWNNA

EXTRA-Meso (EXercise TheRApy in Mesothelioma) Feasibility

Sponsor: NHS Greater Glasgow and Clyde

NCT ID: NCT06491784

View on ClinicalTrials.gov ↗

At a glance

What the study gets you
Access to the study treatment being tested
Type of study
Interventional (receives a drug or procedure)
Time in hospital
In-person visits at study sites — visit count not specified by the sponsor
Drug or intervention
Exercise Therapy (other)
How long the study runs
Study runs about 18 months (dates as stated)
About the drug or intervention
Exercise Therapy — other: 12 week personalised exercise, nutrition and wellbeing programme
Patient visit burden
Not specified by the sponsor
Type of study
Testing a treatment
Ages
18 Years and over
Who
All
Number of participants
40
Started
2024-01-25
Last checked
2024-07

Plain English Summary

What is this study?

  • • Testing a new treatment for mesothelioma
  • • NA - 40 participants
  • • The goal of this clinical trial is to learn whether running an exercise study in patients with mesothelioma is feasible

Who can take part?

  • • Ages 18 Years and over
  • • Diagnosed with mesothelioma

Where?

  • • Glasgow - Queen Elizabeth University Hospital
  • • Manchester - Wythenshawe Hospital

This is a simplified summary. Always discuss with your doctor before making any decisions.

About This Trial

The goal of this clinical trial is to learn whether running an exercise study in patients with mesothelioma is feasible. The main question(s) it aims to answer are: 1. Is it feasible to recruit patients to a randomised clinical trial of exercise therapy 2. What are the barriers to study recruitment 3. What are the barriers to study retention Participants who decide to take part in the study will be randomly allocated one of two study arms: 1. Standard of care, where the participant will undergo their usual clinical follow-up 2. Exercise therapy, where the participant will receive a personalised 12 week exercise, nutrition and wellbeing programme Participants in both study arms will be asked to complete quality of life questionnaires and a basic fitness assessment at the start and end of the study follow-up period. Participants will be asked if they would be happy to conduct a short interview with a member of the research team, to assess their views on the study. This interview will be audio recorded and the audio recording will be transcribed anonymously to allow researchers to improve future study design.

More detail

The aim of this study is to examine the feasibility of a randomised trial of exercise therapy in Mesothelioma. It will define likely rate of recruitment based on performance in two mesothelioma centres and identify barriers to recruitment and retention. Outcomes from the study will help refine the design of a future definitive phase 3 trial. That future phase 3 trial will have a patient-centred primary endpoint, e.g. a meaningful improvement in Health Related Quality of Life (HRQOL) or an increase in treatment uptake or tolerance. Additional outcome measures are likely to include functional fitness, hospital admissions and overall survival. A randomised prospective feasibility study will be performed over 12 months in two centres in the United Kingdom (Glasgow and Manchester). If eligible for the study, patients will be randomised 1:1 to receive a personalised exercise programme or standard care. Patients randomised to the intervention (exercise) arm will undergo an individualised assessment by either a physiotherapist or a qualified exercise specialist with specialised exercise and health condition qualifications. Following this initial assessment, patients will receive a tailored exercise, wellbeing and nutritional support package. The investigators will assess functional fitness and health-related quality of life scores as study outcome measures. The investigators also aim to conduct semi-structured interviews in patients who decline to participate or drop out of the study in order to examine barriers to study recruitment and retention.

Mesothelioma

How this trial compares with your answers

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What we know so far

Condition· Matched your search
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Still need:

  • • Tell us your age for better matching
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Preliminary match based on your answers. Full eligibility requires on-site assessment including medical history, physical exam, and lab tests. This does not guarantee enrolment.

Eligibility at a Glance

Key info

  • Age: 18 Years and over
  • Who can join: All genders

What the study is looking for

  • ✓Diagnosis of mesothelioma, ratified by a mesothelioma multi-disciplinary team (MDT) meeting
  • ✓Performance status 0 - 2
  • ✓Clinical frailty score ≤5
  • ✓Informed written consent

Who cannot take part

  • ✗Performance status ≥3
  • ✗Clinical frailty score ≥6
  • ✗Unlikely to be able to participate in an exercise programme (clinician/physiotherapist judgement)
See the full criteria
Inclusion Criteria: 1. Diagnosis of mesothelioma, ratified by a mesothelioma multi-disciplinary team (MDT) meeting 2. Performance status 0 - 2 3. Clinical frailty score ≤5 4. Informed written consent Exclusion Criteria: 1. Performance status ≥3 2. Clinical frailty score ≥6 3. Unlikely to be able to participate in an exercise programme (clinician/physiotherapist judgement)

Where Is This Study? (2 UK sites)

Queen Elizabeth University Hospital

Glasgow G51 4TF, United Kingdom

Recruiting
Site contact (verified)
Selina Tsim, PhDPrincipal Investigator

Wythenshawe Hospital

Manchester M23 9LT, United Kingdom

Recruiting
Site contact (verified)
Matthew Evison, MDPrincipal Investigator

How to Get in Touch

Selina Tsim, PhD

Sponsor contact

CONTACT

0141 451 6163 Selina.Tsim@glasgow.ac.uk
Data sourced from ClinicalTrials.gov · Last verified: 2024-07