RecruitingNCT07147621

Evaluation of Chemotherapy-induced Cognitive Disorders During the Treatment of Hematological Malignancies


Sponsor

University Hospital, Angers

Enrollment

120 participants

Start Date

Feb 26, 2026

Study Type

OBSERVATIONAL

Conditions

Summary

Chemotherapy-induced cognitive disorders, such as memory problems, slowness of execution, inability to concentrate, and language difficulties, are sequelae that occur in patients undergoing chemotherapy or who have received chemotherapy. These symptoms lead to a degradation of the patients' quality of life and can have a significant social and familial impact. They are most commonly described in solid oncology, particularly in patients with breast cancer. Data about patients with hematological malignancies are scarce, but they seem to show the same phenomenon as in solid oncology. Indeed, many chemotherapies are used both in hematology and solid oncology and may therefore cause similar effects on cognition. Additionally, due to their mechanism of action, some chemotherapies specifically used in hematology could induce cognitive disorders. Hematology-treated patients are probably also affected by these disorders and may consequently experience a reduced quality of life. The objective of this study is to assess the changes in cognitive functions in patients receiving chemotherapy for the treatment of hematological malignancies, using neuropsychological tests and a self-administered questionnaire, compared to a control group, as well as their potential impact on quality of life, fatigue, anxiety, and depression.


Eligibility

Min Age: 18 Years

Plain Language Summary

Simplified for easier understanding

This study is examining whether chemotherapy for blood cancers (like leukemia or lymphoma) causes memory and thinking problems — sometimes called "chemo brain." Researchers will compare cognitive function in patients undergoing treatment to a healthy comparison group. **You may be eligible if...** - You are an adult diagnosed with acute myeloid leukemia, Hodgkin's lymphoma, or non-Hodgkin's lymphoma - You are about to begin your first course of chemotherapy (fixed duration) - OR you are a healthy adult (relative of a patient) of similar age and education level willing to serve as a comparison participant **You may NOT be eligible if...** - You have previously received chemotherapy or treatments that affect the brain - You have pre-existing cognitive or neurological conditions - (For the control group) You are not within 5 years of age or do not match the education level of a participating patient Talk to your doctor to see if this trial is right for you.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Locations(1)

University Hospital of Angers

Angers, Maine et Loire, France

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NCT07147621


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