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The impact of cognitive training on cognitive outcomes following coronary artery bypass grafting surgery in older adults.

Reducing delirium and dementia risk: A cognitive training intervention of older adults undergoing elective coronary artery bypass grafting surgery.

Status
Completed
Phases
Unknown
Study type
Interventional
Source
ANZCTR
Registry ID
ACTRN12618000799257
Acronym
The Cognitive CABG Study, CCABG
Enrollment
45
Registered
2018-05-10
Start date
2018-05-15
Completion date
2021-09-01
Last updated
2023-09-18

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

Conditions

None listed

Brief summary

Older adults are increasingly having operations on their heart, which improves heart function however often leads to problems with learning and memory (cognitive impairment). These adults are already at high risk of dementia due to poor heart health, therefore this cognitive impairment after surgery puts them at even greater risk of late-life dementia. This project aims to decrease future dementia risk following heart surgery, in 120 patients 65 years and older, using cognitive training interventions. Learning and memory will be measured at the beginning of the study, so any changes can be assessed following surgery. The cognitive interventions will take place both before and after surgery in half of the patients. Cognitive impairment (such as delirium) will be monitored in hospital and learning and memory will be tested 4 and 6 and 12 months, and 1 and 3 years post-surgery. It is expected that patients who undertake cognitive training will demonstrate better learning and memory after surgery compared to patients who did not.

Interventions

The HappyNeuron Pro cognitive training platform will be utilised to deliver the cognitive training within the study. There will be two cognitive training intervention time points throughout the study. The first is pre-surgery, starting immediately after completing their baseline session, and involve approximately 2 weeks of training. The second intervention will begin 1-month after the participant has had their surgery and will involve 12 weeks of cognitive training. The same participants who co

The HappyNeuron Pro cognitive training platform will be utilised to deliver the cognitive training within the study. There will be two cognitive training intervention time points throughout the study. The first is pre-surgery, starting immediately after completing their baseline session, and involve approximately 2 weeks of training. The second intervention will begin 1-month after the participant has had their surgery and will involve 12 weeks of cognitive training. The same participants who complete pre-surgery cognitive training will complete post-surgery intervention. The cognitive training intervention will be in addition to normal care pre and post-surgery, and the intervention will be conducted outside of any needed hospital visits so not to disrupt normal care. Within the cognitive training program, each session has been planned and is identical across participants (each session equally trains targeted domains; pyscho-motor speed, attention, memory and executive function). However, the program is still personalised as each exercise has 9 levels and allows participants to level up through the exercises at different rates (consistent high performance increases the level, consistent low performance results in levelling down). For participants randomised into the cognitive training, the training intervention will be home-based and conducted on either a participant’s personal laptop or on a supplied University laptop. The duration of the sessions will be 45 minutes of completed cognitive training (if break wanted/needed then extend session. E.g. 3 minute break; session extends to 48 minutes). The session frequency pre-surgery will be every other day (3.5 times a week), post-surgery this frequency will be decreased to 3 times a week. Pre-surgery cognitive training: The initial session will be instructed and supervised, with an emphasis being placed on participant understanding and competence of system use. Participants will complete 45 minutes of cognitive training every other day over a two week period following baseline testing (total of approximately 7 sessions). Post-surgery cognitive training: This second program will last for a longer duration (compared to pre-surgery) of 12 weeks. Between their pre- and post-surgery interventions participants will be prohibited from using their cognitive training log in. The initial session will yet again be supervised. The post-surgery intervention will be conducted for twelve weeks with 45 minute sessions three times a week (total of 27 hours). Following the completion of the intervention, participants will be informed and prohibited from using the cognitive training system until the commencement of the final follow-up session (3 years post-surgery). To support participants with their cognitive training and to help with adherence, multiple strategies have been put in place. Firstly weekly, face-to-face interventions will be offered to the participants to support any person who may be having difficulties. If individual participants require further support, multiple face-to-face sessions/ phone calls or other support will be organised. Weekly phone calls will also be made to check in on participants, and allow them to ask any questions. An instruction booklet will be provided to participants with information of how to use the program and outline technical troubleshooting. Within the booklet contact information of the cognitive training members of the research team is provided for any further questions. The members of the research team have been trained by Dr Amit Lampit, a cognitive training expert with experience in running large cognitive training interventions.

Sponsors

The University of South Australia
Lead SponsorUniversity

Study design

Allocation
Randomised controlled trial
Intervention model
Parallel
Primary purpose
Prevention
Masking
Blinded (masking used) (Outcomes Assessor)

Eligibility

Sex/Gender
All
Age
65 Years to No maximum
Healthy volunteers
No

Inclusion criteria

Persons must be undergoing elective CABG surgery at the Royal Adelaide Hospital aged 65 years and over. Must be proficient English speakers, have normal vision and hearing with or without the use of aids, live within metropolitan boundaries of Adelaide (Development Act 1993) and be willing to participate in a longitudinal study with follow-up sessions.

Exclusion criteria

* Known learning disabilities or dementia diagnosis, a significant neurological/ psychiatric diagnosis (all factors will affect ability to perform assessments) * History of cancer treatment within the past 5 years (excluding pure surgical treatment) [as cancer treatment is known to negatively affect cognition ]). * Suffered a stroke within the past year (many stroke related cognitive impairments subside within a year) * Currently practicing cognitive training (will interfere or muddle cognitive training effects).

Outcome results

None listed

Source: ANZCTR · Data processed: Feb 19, 2026