Clinical Trials Directory

Trials / Recruiting

RecruitingNCT06280885

A Flexible Individualized ExeRcise Programme for Cancer Patients During ChEmotherapy

Status
Recruiting
Phase
N/A
Study type
Interventional
Enrollment
50 (estimated)
Sponsor
University of Dublin, Trinity College · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

The primary aim of this study is to measure the feasibility of delivering a co-designed exercise programme for patients with cancer receiving chemotherapy treatment.

Detailed description

Exercise has been shown to play an important role in reducing many of the side effects associated with chemotherapy treatment. Exercise can help to improve symptoms of fatigue, nausea, muscle weakness, and pain, which in turn can help to improve patients overall quality of life and wellbeing. In addition to this, exercising during chemotherapy can also help to maintain physical fitness and preserve muscle mass, which has been shown to significantly reduce treatment toxicities. Despite these benefits of exercise, performing regular physical activity during chemotherapy poses significant challenges. Patients are faced with a number of physical and logistical barriers during chemotherapy which makes it difficult to engage in regular exercise. In addition to this, exercise programs that are being designed lack flexibility and individualization, and don't account for the unpredictable nature of chemotherapy treatment. It is, therefore, no surprise that patients struggle to meet the exercise recommendations during chemotherapy, and highlights the need for careful consideration when prescribing exercise during this time. In preparation for this study, the research team held a number of workshops which included a mixture of patients and healthcare professionals with the aim of co-designing an exercise intervention for patients during chemotherapy. Including public and patient involvement (PPI) in the design process will help to ensure that the exercise program that is developed is pragmatic and, most importantly, patient-centred.

Conditions

Interventions

TypeNameDescription
BEHAVIORALExerciseParticipants will be randomised to either the FIERCE exercise programme involving supervised exercise prescription
BEHAVIORALHealth Behaviour Change (Pedometer)Participants in both arms will be provided with a pedometer as a health behaviour change intervention

Timeline

Start date
2025-01-01
Primary completion
2025-09-01
Completion
2026-03-31
First posted
2024-02-28
Last updated
2025-02-03

Locations

1 site across 1 country: Ireland

Source: ClinicalTrials.gov record NCT06280885. Inclusion in this directory is not an endorsement.