Acute Myeloid Leukemia (AML) Clinical Trials

Find Acute Myeloid Leukemia (AML) Clinical Trials Near You

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

Status: Recruiting
Location: See location...
Study Type: Observational
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
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: t
View:

• Patient group inclusion criteria:

‣ adult patient with acute myeloid leukemia, Hodgkin's lymphoma, or non-Hodgkin's lymphoma;

⁃ patient receiving a fixed-duration first-line chemotherapy;

⁃ patient affiliated or beneficiary of a social security scheme; .signed inform consent form.

• Control group inclusion criteria:

‣ adult;

⁃ patient's relative (spouse, brother, sister, friend, etc.);

⁃ less than 5 years of difference with the patient;

⁃ same educational level (\< baccalaureate/high school degree, baccalaureate/high school degree level, 2-year university degree, \> 2-year university degree);

⁃ person affiliated or beneficiary of a social security scheme;

⁃ signed informed consent form

Locations
Other Locations
France
University Hospital of Angers
RECRUITING
Angers
Contact Information
Primary
SCHMIDT ALINE, MD, PhD
AlSchmidt@chu-angers.fr
2 41 35 44 82
Backup
Darras Elise, PharmD
Elise.Darras@chu-angers.fr
241355925
Time Frame
Start Date: 2026-02-26
Estimated Completion Date: 2027-10
Participants
Target number of participants: 120
Treatments
patient group
control group
Sponsors
Leads: University Hospital, Angers

This content was sourced from clinicaltrials.gov

Similar Clinical Trials