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Contact the study team using the details below to take part. If there are no contact details below please ask your doctor in the first instance.

Contact Information:

Lauren Heathcote
Lauren.heathcote@kcl.ac.uk


Emily Dowling
Emily.j.dowling@kcl.ac.uk


More information about this study, what is involved and how to take part can be found on the study website.

Study Location:

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Be Part of Research - Trial Details - EMBody

EMBody

Completed

Open to: Female / Male

Age: 16 Years - 25 Years

Medical Conditions

Malignant neoplasms of bone and articular cartilage
Malignant neoplasms of eye, brain and other parts of central nervous system
Malignant neoplasms of ill-defined, secondary and unspecified sites
Malignant neoplasms, stated or presumed to be primary, of lymphoid, haematopoietic and related tissue


This information is provided directly by researchers, and we recognise that it isn't always easy to understand. We are working with researchers to improve the accessibility of this information. In some summaries, you may come across links to external websites. These websites will have more information to help you better understand the study.


Survivors of childhood cancer experience impaired health-related quality of life, psychological distress, and pain. A previously developed body mindset intervention has improved health-related quality of life and symptom distress in adult cancer patients. In the current research, we will examine whether a body mindset intervention can instil adaptive body mindsets, boost resilience, and improve physical and psychological functioning in survivors of childhood cancer.

Survivors of childhood cancer will be randomised to the body mindset intervention or an active attention control group. The body mindset intervention aims to instil adaptive mindsets that the child’s body is resilient, working with them rather than against them, and is capable of healing after cancer treatment and that an experience of cancer can be an opportunity. Participants receiving the body mindset intervention will complete three modules over six-weeks consisting of short films and reflection exercises to guide participants to more adaptive body mindsets. Participants in this group will also complete a range of questionnaires at baseline, weeks two, four, and six, and at a 10-week and 3-month follow-up.

Participants in the active attention control group complete the same questionnaires at baseline, weeks two, four, and six, and at a 10-week and 3-month follow-up. Therefore, the purpose of the active attention control group is to control for completing online surveys and engaging with the research team to receive surveys.

Survivors of childhood cancer aged 16-25 will be recruited from The Royal Marsden Hospital, University College London Hospital (UCLH), and University Hospital Southampton (UHS). Clinicians at the hospitals will screen medical records and contact those who are eligible to provide information about the study. Overall, we predict that the body mindset intervention will increase adaptive body mindsets, reduce maladaptive body mindsets, and improve health-related quality of life, resilience, psychological and physical functioning compared to the active attention control group.

Start dates may differ between countries and research sites. The research team are responsible for keeping the information up-to-date.  

The recruitment start and end dates are as follows:

18 Oct 2024 05 Sep 2025

Interventional

Interventional type: Psychological & Behavioural;



You can take part if:



You may not be able to take part if:


Participants will be excluded if they have significant cognitive impairment that would precede engagement with the digital intervention or completion of self-report questionnaires. This information will be self-reported by the patient, caregiver or clinical team member.


Below are the locations for where you can take part in the trial. Please note that not all sites may be open.

  • John Radcliffe Hospital
    Headley Way
    headington
    Oxford
    Oxfordshire
    OX3 9DU

Lauren Heathcote
Lauren.heathcote@kcl.ac.uk


Emily Dowling
Emily.j.dowling@kcl.ac.uk



More information about this study, what is involved and how to take part can be found on the study website.


The study is sponsored by King's College London and funded by MEDICAL RESEARCH FOUNDATION .




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for Trial ID: CPMS 59180

Last updated 17 March 2026

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