Actively Recruiting
Chemotherapy Induced Cognitive Impairment
Led by University of Aberdeen · Updated on 2026-05-08
50
Participants Needed
1
Research Sites
211 weeks
Total Duration
On this page
Sponsors
U
University of Aberdeen
Lead Sponsor
N
NHS Grampian
Collaborating Sponsor
AI-Summary
What this Trial Is About
Chemotherapy is toxic and challenges everyone differently. Most chemotherapy side-effects are known and well documented. However, the phenomenon of "chemo fog" also known as "chemobrain" has not been fully investigated and is often based on comments of breast cancer patients attending outpatient clinics during and after their chemotherapy. Changes in thinking ability like lack of concentration, loss of memory and the inability to hold a thought or even a conversation has a significant impact on the lives of breast cancer patients. Without understanding what "chemobrain" is, and what causes it, there is little that doctors can do to help at the moment. The team proposing this study believe that chemotherapy causes chemicals associated with inflammation to attack parts of the brain that are important for concentration and making new memories. Unfortunately, it is not possible to measure these chemicals directly in the brain, but we believe that a brain scan sensitive to excess iron, a marker of brain inflammation, can help. This project will measure thinking ability, such as memory and concentration, take a blood sample and do a brain scan before, during and after a patient has chemotherapy. We will then look for changes in iron in the brain areas that are important for concentration and memory and compare those to changes in thinking ability and to levels of inflammation chemicals in the blood. This information will be essential to help plan our next step which is to test ways to reduce the effects of "chemobrain".
CONDITIONS
Official Title
Chemotherapy Induced Cognitive Impairment
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Women and men >18 years
- Diagnosed with HER2 negative breast cancer
- Receiving EC-Taxane or Taxane only based chemotherapy
- Able to communicate in English
- Willing and able to give informed consent for participation in the study.
You will not qualify if you...
- Any patient whose physical condition will preclude them from lying still for the duration of the brain scan.
- Pre-existing mental condition or disability
- Contraindication to magnetic resonance scanning such as an implantable cardiac device.
AI-Screening
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Trial Site Locations
Total: 1 location
1
NHS Grampian
Aberdeen, United Kingdom
Actively Recruiting
Research Team
T
Teresa Morris
CONTACT
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
1
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