Leukaemia 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 people with blood cancer receiving TKI treatment:
- People who have been diagnosed with CML (chronic myeloid leukaemia) or CLL (chronic lymphocytic leukaemia)
- People who are due to receive their first dose of a TKI (a type of targeted cancer medication) within the next 30 days, or who received their first dose within the past 30 days
- People who are 18 years of age or older
- People who can speak and read English
- People who are able to understand the study and are willing to sign a consent form
For cancer-free people joining as a comparison group:
- People who are 18 years of age or older
- People who can speak and read English
- People who are able to understand the study and are willing to sign a consent form
- People whose age is within 5 years (older or younger) of a matched participant in the cancer group, and who are the same sex as that participant
Who may not be able to join:
- People who have a history of cancer that has spread to other parts of the body, a primary brain tumour, or radiation treatment to the brain
- People who have previously received TKI therapy at any point
- People who have received certain other cancer treatments — including chemotherapy, immune checkpoint therapy, hormonal therapy, biologic therapy, or radiotherapy — within the past 5 years (note: prior use of hydroxyurea for CML or CLL, or use of obinutuzumab or rituximab alongside TKI therapy for CLL, are exceptions and may still be permitted — confirm with trial site)
- People who have had a stroke within the past year, or who still have ongoing thinking or memory difficulties from a stroke that occurred more than a year ago
- People who have had a head injury with loss of consciousness within the past year
- People who have been diagnosed with dementia or a serious condition affecting the brain and nervous system that impacts daily life
- People who have been hospitalised for a psychiatric condition within the past year
- People who are currently pregnant
- People who report being colour blind
- People who are staff members on this study and have previously seen or administered the cognitive tests being used (such as CANTAB)
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 Janelsins, PhD, University of Rochester NCORP Research Base
Phone: 585-275-1090
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
Subjective cognitive performance
Can't join this trial?
Data last synced from ClinicalTrials.gov: 23 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.