- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07452276
Artificial Intelligence-Based Cognitive Training in Patients With Stroke (AICoRe-Stroke)
Effect of Artificial Intelligence-Based Training on Cognitive Functions in Patients With Stroke
This study would answer the following question:Does AI application-based training improve cognitive function in Patients with Stroke?
The aims of this study:
To investigate the efficacy of AI application-based training on cognitive function in stroke patients.
Study Overview
Status
Study Type
Enrollment (Estimated)
Phase
- Not Applicable
Contacts and Locations
Study Contact
- Name: Omima Alaa Eldin Hussein
- Phone Number: +201207838324
- Email: omimaalaa27@gmail.com
Study Locations
-
-
Egypt
-
Cairo, Egypt, Egypt, 62517
- Recruiting
- Physical therapy- Cairo University
-
Contact:
- Omima Alaa Eldin Hussein
- Phone Number: +201207838324
- Email: omimaalaa27@gmail.com
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
Patient's age will range from 45- 60 years.
- Diagnosis of stroke in the chronic stage (≥3 months post-onset).
- Presence of cognitive impairment confirmed by a Montreal Cognitive Assessment (MoCA) score ≤ 26.
- Medically stable and able to follow instructions.
- patients with memory deficits following stroke
Exclusion Criteria:
- Patients will be excluded if they have:
- Severe visual, hearing, or speech impairments prevent participation.
- History of other neurological or psychiatric disorders.
- Unstable cardiovascular or systemic disease.
- Severe depression (Beck Depression Inventory > 29).
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Double
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: AI-Based Cognitive Training
Participants receive artificial intelligence-based cognitive training in stroke patients.
The AI program is designed to target multiple cognitive domains including attention, memory, executive function, and processing speed.
|
A structured artificial intelligence-based cognitive training program targeting attention, memory, executive function, and processing speed in patients with stroke.
The program provides adaptive, individualized exercises based on participant performance.
|
|
Active Comparator: Conventional Physical Therapy
Participants receive a conventional rehabilitation program consisting of aerobic exercises, relaxation exercises, and traditional paper-based cognitive exercises, in addition to standard physical therapy.
|
A structured conventional rehabilitation program consisting of aerobic exercises, relaxation exercises, and traditional paper-based cognitive exercises for patients with stroke.
The duration and frequency of treatment are matched to the experimental group.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Change in Cognitive Function
Time Frame: Baseline and 6 weeks post-intervention
|
Change in Global Cognitive Function Measured by the Montreal Cognitive Assessment (MoCA) Global cognitive function will be assessed using the Montreal Cognitive Assessment (MoCA), a one-page, 30-point cognitive screening tool that evaluates attention, memory, executive function, language, visuospatial abilities, abstraction, calculation, and orientation. The test takes approximately 10 minutes to administer. Scores range from 0 to 30, with higher scores indicating better cognitive function. A score of less than 26 indicates cognitive impairment. |
Baseline and 6 weeks post-intervention
|
Collaborators and Investigators
Sponsor
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Estimated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
- Cerebrovascular Disorders
- Brain Diseases
- Central Nervous System Diseases
- Nervous System Diseases
- Vascular Diseases
- Cardiovascular Diseases
- Stroke
- Therapeutics
- Patient Care
- Health Services
- Health Care Facilities Workforce and Services
- Rehabilitation
- Aftercare
- Continuity of Patient Care
- Neurological Rehabilitation
- Cognitive Training
Other Study ID Numbers
- P.T.REC/012/006268
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
product manufactured in and exported from the U.S.
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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