Breast 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:
All participants:
- People who identify as female, based on their medical records or self-report
- People who are currently between the ages of 60 and 80
- People who have access to a computer and internet connection
- People who score below 11 on a short memory and thinking test called the Blessed Orientation-Memory-Concentration Test (BOMC) (confirm with trial site)
- People who, if currently taking medications that affect mood or mental health (such as antidepressants or anti-anxiety medications), have been on a stable dose for at least two months before joining
- People who speak English fluently and can hold a reasonable conversation in English, as confirmed by trial staff
Breast cancer survivors (in addition to the above):
- People with a history of stage 0 to 3 breast cancer that was first diagnosed between the ages of 50 and 60
- People who currently have no signs of active cancer (known as "no evidence of disease")
People with no cancer history (control group, in addition to the general criteria above):
- People who have never had breast cancer
Who may not be able to join:
All participants:
- People who have been diagnosed with a condition that affects brain function, such as Alzheimer's disease, Parkinson's disease, multiple sclerosis, dementia, or seizure disorders
- People who have had a stroke or a head injury that caused lasting brain changes, ongoing thinking or memory difficulties affecting daily life, or required cognitive rehabilitation
- People who have been diagnosed with certain serious mental health conditions, including schizophrenia-related disorders, bipolar disorder, schizotypal personality disorder, or substance use disorder
- People with vision or hearing problems severe enough to prevent them from completing the study assessments, even with glasses or hearing aids
- People who take the medications methotrexate or rituximab for rheumatoid arthritis, psoriasis, or Crohn's disease, or cyclophosphamide for lupus
- People who are already taking part in a conflicting research study that involves overlapping brain and thinking assessments (specifically study MSK 18-294)
Breast cancer survivors:
- People whose breast cancer has come back (recurrence)
- People who have had any other type of cancer, except non-melanoma skin cancer (a second breast cancer also makes someone ineligible)
- People whose breast cancer was treated with surgery only, with no other treatments
People with no cancer history (control group):
- People who have previously been treated with radiation, chemotherapy, tamoxifen, or aromatase inhibitors
- People who have had any history of cancer, except non-melanoma skin cancer
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: James Root, PhD, Memorial Sloan Kettering Cancer Center
Phone: 646-888-0035
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
examine cognitive effects
Can't join this trial?
Data last synced from ClinicalTrials.gov: 7 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.