Brain Cancer Trial, Recruiting
Who may be able to join
AI generated eligibility summary. Written by an AI model from the official source data and checked on a sample basis. It can contain mistakes, so confirm anything important against the original source. How we use AI
Who might be able to join this trial:
For breast cancer patient participants:
- Women who have been diagnosed with invasive breast cancer that has not spread to other parts of the body (stages I through IIIC)
- People who are scheduled to start a chemotherapy treatment plan using the drugs Adriamycin and Cytoxan
- People who have never received chemotherapy before
- People who are able to speak and read English
- People aged 21 or older
- People who are willing to sign a written consent form
For control participants (people without breast cancer who take part for comparison):
- Women who are within 5 years of age of a breast cancer participant in the trial
- People who are able to speak and read English
- People aged 21 or older
- People who are willing to sign a written consent form
Who may not be able to join:
For breast cancer patient participants:
- People who are currently in hospital, or who have been hospitalised in the past year due to a mental health condition
- People who have been diagnosed with a disease that causes the brain or nervous system to break down over time, such as Alzheimer's or Parkinson's disease
- People who have a condition affecting the brain or central nervous system, such as multiple sclerosis or a movement disorder
- People who have had a mini-stroke (TIA) or stroke within the past year, or who still have symptoms from a past TIA or stroke (confirm with trial site)
- People who are scheduled to receive radiation treatment at the same time as chemotherapy
- People who are colorblind
For control participants:
- People who are currently in hospital, or who have been hospitalised in the past year due to a mental health condition
- People who have been diagnosed with a disease that causes the brain or nervous system to break down over time, such as Alzheimer's or Parkinson's disease
- People who have a condition affecting the brain or central nervous system, such as multiple sclerosis or a movement disorder
- People who have had a mini-stroke (TIA) or stroke within the past year, or who still have symptoms from a past TIA or stroke (confirm with trial site)
- People who have previously been diagnosed with cancer or received chemotherapy
- People who are colorblind
For the optional brain scan sub-study:
- MRI safety screening is required to determine whether participation in the optional scanning portion of the study is appropriate (confirm with trial site)
Important: Always verify eligibility with the trial site directly before applying.
Based on publicly available eligibility criteria from ClinicalTrials.gov. Verify directly with the trial site before acting. This is not medical advice.
Contact this trial
Principal Investigator: Michelle C. Janelsins, Ph.D.,M.P.H., University of Rochester
Phone: 585-273-3998
Contact details sourced from ClinicalTrials.gov. Verify directly with the trial site before attending.
GP referral letter
Print a one-page summary to share with your doctor.
Trial details
Where this trial is recruiting
Primary endpoints
Cognitive function (memory, concentration, attentiveness) will be assessed by computerized cognitive assessments and associated with inflammation and neurotoxicity markers
Can't join this trial?
Data last synced from ClinicalTrials.gov: 14 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.