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Effects of Computer Assisted Cognitive Rehabilitation on Patients With Stroke

E

Ege University

Status

Unknown

Conditions

Stroke

Treatments

Behavioral: Computer Assited Cognitive rehabilitation
Behavioral: Conventional Cognitive Rehabilitation

Study type

Interventional

Funder types

Other

Identifiers

NCT03890159
Stroke-CACR

Details and patient eligibility

About

This study aims to investigate the effects of computer assisted cognitive rehabilitation and conventional cognitive rehabilitation methods on patients' attention, quality of life and functional independence. Recruiting from 15 patients from each group, patients will be followed up for a month and the outcome measures will be repeated.

Enrollment

45 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Patients over 18 years of age with stroke

Exclusion criteria

  • Problems with sight
  • Comorbid neurological disease
  • Cognitive impairment prior to stroke
  • Neglect Syndrome
  • Wernicke or Global aphasia

Trial design

Primary purpose

Supportive Care

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Double Blind

45 participants in 3 patient groups

Computer Assisted Cognitive Rehabilitation
Experimental group
Description:
Patients will receive their therapies 1 day a day, 2-3 days a week. The computer-aided cognitive rehabilitation group will perform simulation-based exercises, including exercises related to attention, in a special computer program (Cogniplus TR version) during therapy hours, and patients will progress to the difficulty level automatically. Their performance during this process (response time etc.) will be recorded.
Treatment:
Behavioral: Computer Assited Cognitive rehabilitation
Conventional Cognitive Rehabilitation
Experimental group
Description:
The home (paper pen) exercise group will take the necessary exercises on paper suitable for their respective levels and the daily tasks suitable for their functional needs and interests.
Treatment:
Behavioral: Conventional Cognitive Rehabilitation
Waiting list controls
No Intervention group
Description:
These patients will get no intervention as means of cognitive rehabilitation, but will get their usual treatments.

Trial contacts and locations

0

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Central trial contact

Hale Karapolat, M.D.

Data sourced from clinicaltrials.gov

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