Efficacy of neurocognitive rehabilitation after CABG surgery in improving quality of life

Not Applicable

• Conditions: cognitive deficit.; Other specified cognitive deficit; R41.84

• Registration Number: IRCT2017022132704N1
• Lead Sponsor: Cognitive Sciences and Technologies Council

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 14 January 2019

Recruitment & Eligibility

• Status: Complete
• Sex: All
• Target Recruitment: 75

Inclusion Criteria

Male or female outpatients.
Aged between 40 and 80.
Capable of perception of the research nature.
Able to give informed consent before any study is written.
Capable to speak in Persian with study personnel.
Able to read and write and work with computer.
Participation in concurrent standard routine rehabilitation during the trial.

Exclusion Criteria

Dependency on alcohol or drugs.
Has any mental disorders that might interfere with the exact assessment or accuracy of treatment.
Has any clinical conditions that cause the usage of prescribed drugs that could have any effect on the Attention.

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Selective attention. Timepoint: pre-intervention, post-intervention, 6-month follow-up. Method of measurement: Flanker test.;Sustained attention. Timepoint: pre-intervention, post-intervention, 6-month follow-up. Method of measurement: Continuous Performance test.;Divided attention. Timepoint: pre-intervention, post-intervention, 6-month follow-up. Method of measurement: Useful Field of View.;Working memory. Timepoint: pre-intervention, post-intervention, 6-month follow-up. Method of measurement: Digit Span test (Forward and Backward ).

Secondary Outcome Measures

Name	Time	Method
Quality of life. Timepoint: pre-intervention, post-intervention, 6-month follow-up. Method of measurement: Quality of Life Short Form (SF-36) questionnaire.