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Developing a Rehabilitation Program in Patients with Stroke

Developing a Group Attention Rehabilitation Program and Investigating its Efficacy on Attention and Emotional Outcomes in Patients with Ischemic Stroke

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20230814059142N1
Enrollment
30
Registered
2023-08-21
Start date
2023-09-23
Completion date
Unknown
Last updated
2023-10-16

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Ischemic Stroke. Cerebral infarction

Interventions

Intervention 1: Intervention group: Group Attention Rehabilitation Program. Intervention 2: Control group: General Education about the Disease and its Course.

Sponsors

Institute for Cognitive Science Studies
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

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

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

Design outcomes

Primary

MeasureTime frame
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

MeasureTime frame
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).

Countries

Iran (Islamic Republic of)

Contacts

Public ContactSajjad Montazerghaem

Institute for Cognitive Science Studies

sajjad.montazerghaem@gmail.com+98 21 7629 1130

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026