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Adaptive Cognitive Training in Healthy Older Adults

Adaptive Cognitive Training in Healthy Older Adults

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02205710
Enrollment
99
Registered
2014-07-31
Start date
2016-08-31
Completion date
2018-08-31
Last updated
2019-08-02

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

Conditions

Alzheimer's Disease, Mild Cognitive Impairment, Mild to Moderate Dementia

Brief summary

Cognitive training has emerged as a promising method to maintain, enhance, and rehabilitate cognitive function in older adults and individuals with dementia. In recent years, such training has become particularly appealing in the clinical context, with many paradigms aimed specifically at adults experiencing various stages of cognitive decline due to Mild Cognitive Impairment, Alzheimer's disease, and vascular dementias. However, basic questions remain. For example, uncertainty persists regarding factors that influence observed improvements as well as the conditions that would maximize transfer and sustainability of training effects. The objective of this study is to evaluate factors that may maximize the benefits of computerized cognitive training in older adults.

Detailed description

The study involves 25 sessions of an adaptive cognitive training program, completed over 5 weeks. Pre and post training assessments will evaluate any near and far transfer effects of training.

Interventions

OTHERComputerized cognitive training
OTHERComputerized games

Sponsors

University of Ottawa
CollaboratorOTHER
Bruyère Health Research Institute.
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
OTHER
Masking
TRIPLE (Subject, Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
60 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

* English as the maternal or primary spoken language. * Good self-reported health (i.e., no cerebro-, or cardio-vascular disease or neurological disease). * Normal or corrected-to-normal vision and hearing.

Exclusion criteria

* Poor hearing or vision * Inadequate understanding of the English language

Design outcomes

Primary

MeasureTime frameDescription
Change in ratings on cognitive training surveyBaseline, week 5This survey aims to assess participant perceptions on cognitive training, and includes a series of related questions, rated on a scale of 1-7.
Change in neural activityBaseline, week 5We will measure resting state as well as task-related EEG responses to determine the effects of cognitive training at the neural level.
Change in performance on neuropsychological testsBaseline, week 5Using a set of standard neuropsychological evaluations, we will measure changes in attention, memory, and executive function following cognitive training.

Secondary

MeasureTime frameDescription
Change in ratings of psychological wellbeingBaseline, week 5We will use standardized questionnaires to assess quality of life, in order to measure the influence of cognitive training on factors related to wellbeing.

Countries

Canada

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026