Lymphoma 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 the patient group:
- Adults diagnosed with acute myeloid leukemia, Hodgkin's lymphoma, or non-Hodgkin's lymphoma
- People who are receiving a set, fixed-length course of first-line chemotherapy (meaning chemotherapy given as the first treatment for their condition)
- People who are covered by a social security scheme
- People who have signed a consent form agreeing to take part
For the comparison (control) group — a close relative or friend of a patient in the trial:
- Adults who are a relative or close contact of a patient participant (such as a spouse, sibling, or friend)
- People whose age is within 5 years of the patient they are paired with
- People who have a similar level of education to the patient they are paired with
- People who are covered by a social security scheme
- People who have signed a consent form agreeing to take part
Who may not be able to join:
For the patient group:
- People who have no suitable relative or close contact available to participate in the control group
- People with known or suspected thinking or memory difficulties that existed before chemotherapy
- People with a history of severe neurological or psychiatric conditions (for example, severe depression)
- People who have previously received chemotherapy
- People who have previously had radiotherapy to the brain
- People currently taking medications that are known to affect thinking or memory
- People who are unable to read
- People who do not speak French
- People who are in custody or subject to a judicial or administrative restriction on their liberty
- People receiving forced psychiatric care
- People under a legal protection order (confirm with trial site)
- People who are unable to give their own consent
- Women who are pregnant or breastfeeding
For the comparison (control) group:
- People with known or suspected thinking or memory difficulties
- People with a history of severe neurological or psychiatric conditions (for example, severe depression)
- People who have previously received chemotherapy
- People who have previously had radiotherapy to the brain
- People currently taking medications that are known to affect thinking or memory
- People who are unable to read
- People who do not speak French
- People who are in custody or subject to a judicial or administrative restriction on their liberty
- People receiving forced psychiatric care
- People under a legal protection order (confirm with trial site)
- People who are unable to give their own consent
- Women who are pregnant or breastfeeding
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
Phone: 2 41 35 44 82
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
Changes in cognitive complaints measured by the Functional Assessment of Cancer Therapy - Cognitive function (FACT-Cog) questionnaire
Can't join this trial?
Data last synced from ClinicalTrials.gov: 19 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.