Cognitive Impairment in Colorectal Cancer Patients Receiving Cytotoxic Chemotherapy
NCT05014399
Chemically-Induced Disorders, Chemo Fog
Fort Wayne, Indiana, United States
View Trial DetailsNCT Number: NCT07842679
This cross-sectional study aims to determine the prevalence of cognitive impairment and evaluate its relationship with activities of daily living among older adults with hematologic malignancies receiving chemotherapy.
Trial opening soon.
Get Notified65 year and older
All sexes
Observational
Cognitive impairment is common among older adults with cancer and may affect treatment adherence and independence. This observational study will include adults aged 65 years or older with confirmed hematologic malignancies who are currently receiving chemotherapy.
Participants will undergo cognitive assessment using the Montreal Cognitive Assessment (MoCA) and functional assessment using the Katz Index of Activities of Daily Living (ADL) and Lawton Instrumental Activities of Daily Living (IADL).
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Time frame: Baseline
Proportion of participants with cognitive impairment defined as a Montreal Cognitive Assessment (MoCA) score less than 26.
Time frame: Baseline
Mean Montreal Cognitive Assessment score (range 0-30).
Time frame: Baseline
Mean Katz Index of Activities of Daily Living score
Time frame: Baseline
Mean Lawton Instrumental Activities of Daily Living score.
Time frame: Baseline
Proportion of participants with impaired Katz ADL score.
Time frame: Baseline
Proportion of participants with impaired Lawton IADL score.
Trial opening soon.
Get NotifiedAssiut University
Other
Prevalence of Cognitive Impairment and Its Association With Activities of Daily Living Among Older Adults With Hematologic Malignancies Receiving Chemotherapy
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