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Study identifier: NCT07511829 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

WearAble Technology for Collecting Health Data in People Who Are the Transfused (WATCH Transfused) - A UK Exploratory Study to Improve Quality of Life and the Efficacy of Transfusion Supportive Care in People With Blood Cancers Undergoing Treatment

Condition: MDS (Myelodysplastic Syndrome) · AML (Acute Myeloid Leukemia)  ·  Sponsor: University of Oxford

PhaseN/A
Planned participants80
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersNo

About this study

Cancer treatments such as chemotherapy often affect healthy cells as well as the cancer cells and this can lead to side-effects such as low blood counts - anaemia. This can cause severe fatigue, shortness of breath and brain fog and may need regular blood transfusions. Their quality of life (QoL) is often very poor during treatment because of these side effects, and it is hard to deal with. Doctors use blood tests to decide whether a patient is well enough for treatment and when to start treatment. However, blood tests do not tell us how a person feels, and it is not the same in everyone. We need a better way for doctors to monitor patients' QoL and these symptoms so that they are physically and emotionally able to continue their treatment. It is hard for doctors to accurately assess this through speaking to their patients and doctors do not record or discuss these effects of treatment very well with patients. The aim of this study is to better understand how people feel during their treatment and how we can best use blood transfusions to maintain QoL. 80 adult patients who are starting blood cancer treatments will be asked to answer questionnaires about how they are feeling and their symptoms during their treatment. Participants will be asked to wear a smartwatch to measure their physical activity levels. Activity data collected will then be compared with their reported QoL and blood counts to help us understand when patients can tolerate difficult treatments the best and…

This description comes directly from the study's public registry record.

Talk to the study team

Matthew H Poynton, MBBS  ·  +447742990230  ·  matthew.poynton@linacre.ox.ac.uk

Always discuss trial participation with your own doctor first.

Locations (1)

Oxford University Hospitals NHS TrustOxford, OXFORDSHIRE, United KingdomRecruiting

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Source record: clinicaltrials.gov/study/NCT07511829