Cognitive Impairment in Older Adults With Hematologic Malignancies
Prevalence of Cognitive Impairment and Its Association With Activities of Daily Living Among Older Adults With Hematologic Malignancies Receiving Chemotherapy
1 other identifier
observational
120
0 countries
N/A
Brief Summary
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 Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P50-P75 for all trials
Started Sep 2026
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
September 21, 2026
CompletedFirst Posted
Study publicly available on registry
September 25, 2026
CompletedStudy Start
First participant enrolled
September 26, 2026
CompletedPrimary Completion
Last participant's last visit for primary outcome
September 26, 2027
ExpectedStudy Completion
Last participant's last visit for all outcomes
February 25, 2028
September 28, 2026
September 1, 2026
1 year
September 21, 2026
September 24, 2026
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Prevalence of cognitive impairment
Proportion of participants with cognitive impairment defined as a Montreal Cognitive Assessment (MoCA) score less than 26.
Baseline
Secondary Outcomes (5)
Mean MoCA score
Baseline
Mean Katz ADL score
Baseline
Mean Lawton IADL score
Baseline
Proportion with impaired activities of daily living
Baseline
Proportion with impaired instrumental activities of daily living
Baseline
Study Arms (1)
Single cohort: Older adults with hematologic malignancies
Adults aged 65 years or older with hematologic malignancies receiving chemotherapy who will undergo cognitive and functional assessment.
Eligibility Criteria
Older adults aged 65 years or older with confirmed hematologic malignancies receiving chemotherapy at Assiut University Hospitals.
You may qualify if:
- \- Age 65 years or older
- Confirmed diagnosis of hematologic malignancy
- Currently receiving chemotherapy
- Able to communicate and participate in cognitive assessment
- Written informed consent
You may not qualify if:
- \- Previously diagnosed dementia before the diagnosis of malignancy
- Delirium at the time of assessment
- Severe visual or hearing impairment interfering with cognitive testing
- History of major neurological disorders affecting cognition
- Severe psychiatric illness affecting cognitive assessment
- Critically ill patients unable to complete study assessment
Contact the study team to confirm eligibility.
Sponsors & Collaborators
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- STUDY CHAIR
Soher M kasem, prof
Internal Medicine Department, Assiut University Hospitals
Central Study Contacts
Study Design
- Study Type
- observational
- Observational Model
- CASE ONLY
- Time Perspective
- CROSS SECTIONAL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Resident Physician, Department of Internal Medicine - Geriatrics
Study Record Dates
First Submitted
September 21, 2026
First Posted
September 25, 2026
Study Start
September 26, 2026
Primary Completion (Estimated)
September 26, 2027
Study Completion (Estimated)
February 25, 2028
Last Updated
September 28, 2026
Record last verified: 2026-09
Data Sharing
- IPD Sharing
- Will not share