Developing a Rehabilitation Program in Patients with Stroke

Not Applicable

Recruiting

• Conditions: Ischemic Stroke.; Cerebral infarction

• Registration Number: IRCT20230814059142N1
• Lead Sponsor: Institute for Cognitive Science Studies

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 16 October 2023

Recruitment & Eligibility

• Status: Recruiting
• Sex: All
• Target Recruitment: 30

Inclusion Criteria

Having Diagnostic Criteria for Ischemic Stroke
Signing the Ethical Consent Form to Participate in the Study (by the person himself/herself or his/her First-Degree Companions)
Age between 18 and 65 years
Being in the Sub-Acute and Chronic Stage of Stroke, according to Specialist Diagnosis
Having the Ability to Read and Write in Persian
Obtaining a score of 22 or lower in Montreal Cognitive Assessment (MoCA)

Exclusion Criteria

Obtaining a score of 10 or lower in Montreal Cognitive Assessment (MoCA)
Having an Unstable Medical Condition, as Diagnosed by a Specialist (eg, Epilepsy or Uncontrolled Diabetes)
Having Other Severe Neuro-Cognitive Disorders, as Diagnosed by a Specialist (eg, Aphasia)
Drug or Alcohol Addiction
Having Movement Limitations that Prevent Training and Intervention Exercises
Getting Another Cognitive Rehabilitation Method

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Sustained Attention. Timepoint: Before the Intervention, After the Intervention, 1 Month after the Intervention. Method of measurement: Integrated Visual and Auditory Continuous Performance Test - 2 (IVACPT - 2) and Trail Making Test - Part A (TMT-A).;Selective Attention. Timepoint: Before the Intervention, After the Intervention, 1 Month after the Intervention. Method of measurement: Stroop Test.;Alternating Attention. Timepoint: Before the Intervention, After the Intervention, 1 Month after the Intervention. Method of measurement: Trail Making Test - Part B (TMT-B).;Divided Attention. Timepoint: Before the Intervention, After the Intervention, 1 Month after the Intervention. Method of measurement: Letter-Number Sequencing Test.

Secondary Outcome Measures

Name	Time	Method
Anxiety. Timepoint: Before the Intervention, After the Intervention, 1 Month after the Intervention. Method of measurement: Beck Anxiety Inventory (BAI).;Depression. Timepoint: Before the Intervention, After the Intervention, 1 Month after the Intervention. Method of measurement: Beck Depression Inventory (BAI).