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

Efficacy of neurocognitive rehabilitation after coronary artery bypass graft surgery in improving quality of life: A randomized controlled trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT2017022132704N1
Enrollment
75
Registered
2017-10-28
Start date
2017-10-17
Completion date
Unknown
Last updated
2019-01-14

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

Conditions

cognitive deficit. Other specified cognitive deficit

Interventions

Intervention 1: CCRT Group:This group of patients is going to receive CCRT plus RCR to activate different cognitive functions including attention, working memory and inhibition.The computerized cognit

Sponsors

Cognitive Sciences and Technologies Council
Lead Sponsor

Eligibility

Sex/Gender
All
Age
40 Years to 80 Years

Inclusion criteria

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

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.

Design outcomes

Primary

MeasureTime frame
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

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

Countries

Iran (Islamic Republic of)

Contacts

Public ContactSimin Sadat Ajtahed

College of Farabi, University of Tehran

s.ajtahed@gmail.com+98 31 5534 1046

Outcome results

None listed

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