An interventional study of ENGAGE SPANISH/MUSIC and ENGAGE DISCOVERY in Subjective Cognitive Decline, sponsored by Centre de Recherche de l'Institut Universitaire de Geriatrie de Montreal. Active, not recruiting at 2 sites in Canada. Open to participants aged 60 Years to 85 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2026-03-17.
Sponsored by Centre de Recherche de l'Institut Universitaire de Geriatrie de Montreal · Not applicable, Interventional, and Prevention
The team "Cognitive intervention, cognitive reserve and brain plasticity", Team 10, is part of the Canadian Consortium on Neurodegeneration in Aging (CCNA). The team's aim is to develop and test a multi-faceted intervention program meant to increase cognitive and brain reserve by providing cognitive stimulation through participation in cognitive training sessions and engaging leisure activities. This will be done with a partially randomized controlled double-blind preference trial with a comprehensive cohort design, in participants with subjective cognitive decline (SCD) recruited in Montreal and Toronto.
In the absence of a cure for Alzheimer's disease (AD), there is paramount interest for non-pharmacological cognitive interventions that are designed to restore, increase, or optimize capacities and adaptation. Numerous epidemiological studies have shown that education, cognitively engaging leisure activities, and cognitively demanding professions are associated with a lower risk of cognitive decline and dementia. When estimating the proportion of AD cases attributable to modifiable risk factors, it was found that cognitive inactivity was the factor that contributed to many of the cases worldwide (19.1% or 6.5 million cases). Thus, the level of cognitive stimulation that individuals receive throughout their life is a critical protective factor against cognitive decline and AD, which suggests potentially powerful avenues for intervention. In a number of influential papers, Stern suggested that differences in cognitive lifestyle contribute to cognitive reserve, defined as the built-up resilience of the brain against the detrimental effect of age-related brain damage. Cognitive stimulation is thought to create richer brain networks and facilitate the recruitment of alternative regions or networks. Barnes and Yaffe projected that 1.375 million AD cases worldwide might be prevented by reducing by 25% the prevalence of cognitive inactivity. These findings have tremendous consequences when designing strategies against dementia. Thus, the goal of Team 10 is to design and test an innovative cognitive training program to increase cognitive reserve and reduce decline in persons with a high risk of AD.
Many studies have shown that cognitive training can increase cognitive abilities in healthy older adults, or persons with mild cognitive impairment (MCI). Studies with MCI also show that cognitive training in MCI results in greater brain activation and connectivity, as well as the recruitment of alternative networks, which supports the view that it contributes to the creation of cognitive reserve.
There are different types of cognitive interventions that are potentially available. Choosing the proper one necessitates a fine understanding of their mechanisms of action and their match to the individual's needs and capabilities. Furthermore, many of the existing programs have not received empirical support from studies relying on good quality methodology and there is a lack of evidence regarding their capacity to reduce cognitive decline and dementia. Hence, previous studies have been limited by some or all of the following methodological issues: 1) they most often relied on a small number of participants; 2) they had time-limited follow-up; 3) many did not use a randomized controlled design or provided limited information on their randomization process; 4) very few have assessed the participant characteristics that define best responders (i.e., the profile of individuals that benefit the most from the intervention). Another important aspect is that the programs that are typically used in those studies are often not optimally adapted to seniors' needs and preferences and are not grounded in real life, limiting adherence and generalization to everyday life. Emotional and cognitive engagement refers to participants enjoying as well as actively participating to the learning experience and has been shown to be a critical factor in determining learning outcomes. Thus, our program will be designed to promote engagement, which is absent in the previous studies. Finally, one other important gap is that there are still a lot that is unknown about the brain processes involved in these interventions and how they alter brain structure and/or function, especially in healthy older adults. Thus, an additional important issue is to understand the brain plasticity processes resulting from cognitive training. Brain plasticity refers to the remarkable ability of the central nervous system to spontaneously re-organize or expand during normal learning processes, or to self-repair in acute or progressive brain diseases. This is critical given that an increasing number of studies has revealed that non-pharmacological interventions can have a positive impact in AD and that intermediate mechanisms of neural plasticity and functional compensation likely modulate the detrimental effect of the disease on symptoms.
The investigators will develop ENGAGE, a program to increase cognitive reserve and reduce decline over a 2-year period in persons with a high risk of AD. The investigators propose a multi-faceted intervention program meant to increase reserve by providing cognitive stimulation through participation in engaging cognitive and leisure activities. This ground-breaking program proposes for the first time to combine (1) hands-on training to improve memory and attention through teaching strategies to optimize efficiency, and (2) selected engaging leisure activities that are known to increase brain functions in younger and older adults, such as learning music, learning a second language, and playing carefully selected casual video-games. There are many reasons to combine brain training and leisure activities. First, one limitation of brain training for memory and attention is that participants sometimes fail to generalize the strategies learned in a lab setting and to apply them in their everyday life. Thus, the investigators propose to practice these strategies in the leisure activities, e.g., to learn information relevant to the music or Spanish lessons. Providing natural, ecologically-valid situations to apply and practice the cognitive strategies is done to train participants to use them more spontaneously outside the formal brain training setting. Second, these leisure activities correspond to the cognitively demanding activities that are identified as protective in epidemiological studies, and thus likely to promote brain plasticity. Third, they are attractive and will therefore improve motivation for training. The enjoyable characteristic of the leisure activities will also make them attractive to older adults with lower education, a segment of population which may especially benefit from such intervention. Finally, if proven effective, the training program will have the important advantage of being easy to implement in the community and will be relatively low-cost relative to formal health care. Another objective of this research project is to provide recommendations regarding profiles of participants which may benefit the most from the intervention. The investigators will thus measure whether the effect of the training is modulated by sex differences as women have been suggested to have less brain reserve than men as well as age, education or socio-cultural background, lifestyle habits, genetic factors and other markers of cognitive reserve.
The research team benefits from the contribution of clinicians and researchers from across Canada who will combine their unique expertise on brain training and on the effects of leisure activities on the brain to provide the most innovative and potentially meaningful approach to cognitive intervention. Overall, this innovative program will provide brain training through specific cognitive training and carefully selected leisure activities that are known to have a positive impact on cognition and will be particularly attractive to older adults from varied backgrounds.
Objectives
Hypotheses. The investigators hypothesize that participants who will be engaged in the intervention program will show better behavioral and brain outcomes than participants from the control group who will receive an active control program. More specifically, improved behavioral performance following the intervention is expected in neuropsychological tests measuring cognitive components that are targeted in the program (mainly memory and attention), as well as a transfer effects to an ecologically-valid test measuring functioning in a simulated real-life situation. The investigators also expect improvement in participants' subjective evaluation of their proficiency and satisfaction with life (questionnaires). Regarding retention of training benefits, the hypothesis is that the experimental group will show better cognition at the follow up testing, 2 years from the beginning of the study, and less cognitive decline when comparing 0- to 2-year performance. Regarding fMRI testing, the investigators expect more task-related activation following training and correlations between brain changes and cognitive gain, which would be considered as a marker of enhanced neurocompensation processes.
Design. The consort guidelines will be used to organize and report the trial (http://www.consort-statement.org). The study uses a randomized controlled double-blind preference trial with a comprehensive cohort design. Outcomes will be tested by assessors who will not be involved in the intervention, and who will be blind to training assignment. One hundred forty-four (144) participants with subjective cognitive decline (SCD), but no objective impairment based on cognitive tests, will be recruited and randomly assigned to either the cognitive program (ENGAGE SPANISH or ENGAGE MUSIC) or the active control program (ENGAGE DISCOVERY). Participants in the ENGAGE DISCOVERY program will undergo the same amount of activities as proposed in the ENGAGE SPANISH/MUSIC programs, but those activities will be designed not to be cognitively challenging. Behavioral measures (objective and subjective measures of cognition and efficiency in everyday life functioning) as well as neuroimaging measures (fMRI scan during a memory task) will be collected at 3 time points: before the intervention (PRE), immediately after the intervention (POST-1), and 2 years after PRE (POST-2). PRE tests will be administered within a 12-week window before the beginning of the intervention. POST-1 and POST-2 will each be administered within a 8-week window.
To ensure that participants will not be enrolled in an activity that they dislike, and thus remain the 'leisure' aspect, they will be able to exclude either the 'Music' or 'Spanish' activity prior to randomization to the intervention or control conditions. This was decided to personalize the intervention as people vary considerably in how attracted they are by different leisure activities, and to give participants a sense of choice, which was found to reduce disappointment related to randomization, and thus to reduce attrition. This will be done in a manner that will allow preserving double blindness. If participants who are randomized in the cognitive program did not wish to exclude an activity, then a second randomization will assign them in one of the 2 activities (either music or Spanish). Thus, the training vs active control comparison is fully randomized but further comparison of the two leisure activities will rely on a partially randomized comparison cohort. In that case, the randomized cohorts will be first compared, followed by a comparison of the entire cohort, including those in the preference arm.
The results of this intervention will be analyzed at three-endpoints: 1) at baseline (PRE); 2) immediately after the intervention (POST-1); and 3) 2 years after baseline, i.e., about 18 months after the end of the intervention (POST-2).
Exclusion Criteria:
Cognitive strategies to improve attention and memory skills and application in selected leisure activities (music or Spanish lessons, and videogames) over 4 months.
Behavioral: ENGAGE SPANISH/MUSIC
Educational program about brain and healthy aging complemented by learning of new information with videogames, documentaries and group discussions over 4 months.
Behavioral: ENGAGE DISCOVERY
Cognitive strategies to improve attention and memory skills (21 hours), leisure activities (music lessons or Spanish lessons) (27 hours), selected videogames to practice variable attention strategies (4 hours in class + about 10 hours at home). Total of 24 2-hour in class sessions over 4 months. The training will be delivered to small groups of 5 to 8 participants by a trained therapist for formal sessions and a professional music or Spanish teacher for leisure sessions.
Educational content about brain and healthy aging (21 hours), leisure activities (watching documentaries followed by group discussion and debate) (27 hours), selected non-stimulating videogames (4 hours in class + about 10 hours at home). Total of 24 2-hour in class sessions over 4 months. The training will be delivered to small groups of 5 to 8 participants by the same trained therapist as in the ENGAGE arm.
Changes in episodic memory (composite score)
A composite score will be computed by averaging z-scores from the delayed recall of the Rey Auditory Verbal Learning Test (RAVLT) and the delayed recall of the face-name association task (an associative memory test adapted from Simona Brambati's task for the Consortium pour l'Identification precoce de la Maladie d'Alzheimer (CIMA-Q) study currently running in Quebec).
Time frame: PRE (within 12 weeks before intervention starts) + POST-1 (within 8 weeks after the end of intervention) + POST-2 (2 years from PRE, +/- 3 months)
Changes in attention control (composite score)
A composite score will be computed by averaging the z-scores from the Number-letter task (switching cost), the complex (4-choice) reaction time from the Canadian Longitudinal Study on Aging (CLSA) Reaction Time Task, and an adapted Flanker task comprising a dual-task condition (congruency effect and dual task cost).
Time frame: PRE (within 12 weeks before intervention starts) + POST-1 (within 8 weeks after the end of intervention) + POST-2 (2 years from PRE, +/- 3 months)
Changes in psychological health: Anxiety and depression (composite score)
A composite score will be computed by averaging the z-scores from the Geriatric Anxiety Inventory (GAI) + Geriatric Depression Scale (GDS).
Time frame: PRE (within 12 weeks before intervention starts) + POST-1 (within 8 weeks after the end of intervention) + POST-2 (2 years from PRE, +/- 3 months)
Changes in psychological health: Apathy
A composite score will be computed that averaging the z-scores from the participant + informant versions of the Apathy Inventory Scale.
Time frame: PRE (within 12 weeks before intervention starts) + POST-1 (within 8 weeks after the end of intervention) + POST-2 (2 years from PRE, +/- 3 months)
Changes in psychological health: Quality of life (composite score)
A composite score will be computed by averaging the z-scores from the 36-item Short Form Survey (SF-36), assessing activities and well-being, and the Quality of Life Alzheimer's Disease questionnaire (QoL-AD).
Time frame: PRE (within 12 weeks before intervention starts) + POST-1 (within 8 weeks after the end of intervention) + POST-2 (2 years from PRE, +/- 3 months)
Changes in psychological health: Help-seeking behaviour
Mean scores from the medical care section from the Stanford Chronic Disease questionnaire, related to medical help-seeking behavior.
Time frame: PRE (within 12 weeks before intervention starts) + POST-1 (within 8 weeks after the end of intervention) + POST-2 (2 years from PRE, +/- 3 months)
Changes in brain structure: Hippocampal Volume (for a subgroup of participants)
Participants will be scanned on a Siemens Total Imaging Matrix (TIM) Trio 3 T magnetic resonance imaging (MRI) system (Siemens Medical Solutions, Erlangen, Germany). Hippocampal volume (mm3) will be measured, as this is an early biomarker of AD and is found to be a sensitive marker of memory training.
Time frame: PRE (within 12 weeks before intervention starts) + POST-1 (within 8 weeks after the end of intervention) + POST-2 (2 years from PRE, +/- 3 months)
Changes in brain structure: Cortical Thickness (for a subgroup of participants)
Participants will be scanned on a Siemens TIM Trio 3 T magnetic resonance imaging (MRI) system (Siemens Medical Solutions, Erlangen, Germany). Cortical thickness (mm) will be measured, as this is an early biomarker of AD and is found to be a sensitive marker of memory training.
Time frame: PRE (within 12 weeks before intervention starts) + POST-1 (within 8 weeks after the end of intervention) + POST-2 (2 years from PRE, +/- 3 months)
Changes in brain function: Brain activation (for a subgroup of participants)
fMRI activity while participants are doing an associative memory task. Participants will be presented a sequence of 80 images (e.g., animals, vegetables, etc.). They appear within one of the four quadrants of the screen. People are asked to remember the images and their position among the 4 quadrants (either top-left, top right, bottom-left or bottom-right). Retrieval is done 10 minutes after the encoding, outside of the scanner. People are presented with the same 78 images in a new order and 39 new images, appearing one at a time in the center of the screen. They have to determine whether each image has been previously presented, and if 'Yes', where it was located.
Time frame: PRE (within 12 weeks before intervention starts) + POST-1 (within 8 weeks after the end of intervention)
Transfer to everyday life (self-reported): Meta-memory rating
Mean scores from the Meta-memory questionnaire (MMQ).
Time frame: PRE (within 12 weeks before intervention starts) + POST-1 (within 8 weeks after the end of intervention) + POST-2 (2 years from PRE, +/- 3 months)
Transfer to everyday life (self-reported): Attention and recent memory rating
Mean scores from the Auto-administered Memory Questionnaire (AMQ, short version).
Time frame: PRE (within 12 weeks before intervention starts) + POST-1 (within 8 weeks after the end of intervention) + POST-2 (2 years from PRE, +/- 3 months)
Transfer to everyday life (self-reported): Activities of daily living
A composite score will be computed that aggregates the average z-scores from the participant + informant versions of the Alzheimer's Disease Cooperative Study - Activities of Daily Living - Prevention Instrument (ADCS-ADL-PI).
Time frame: PRE (within 12 weeks before intervention starts) + POST-1 (within 8 weeks after the end of intervention) + POST-2 (2 years from PRE, +/- 3 months)
Transfer to everyday life (self-reported): Cognitive activities
Mean scores from the Cognitive Activities questionnaire.
Time frame: PRE (within 12 weeks before intervention starts) + POST-1 (within 8 weeks after the end of intervention) + POST-2 (2 years from PRE, +/- 3 months)
Transfer to everyday life (self-reported): Jessen's Questions
The number of participants that do not have a memory complaint.
Time frame: PRE (within 12 weeks before intervention starts) + POST-1 (within 8 weeks after the end of intervention) + POST-2 (2 years from PRE, +/- 3 months)
Transfer to everyday life (performance-based): Instrumental Activities of Daily Living
Mean scores from the Direct Assessment of Functional Status - Revised (DAFS-R), an ecologically-valid task assessing everyday life situations.
Time frame: PRE (within 12 weeks before intervention starts) + POST-1 (within 8 weeks after the end of intervention) + POST-2 (2 years from PRE, +/- 3 months)
Transfer to everyday life (performance-based): Memory Strategies
Mean scores from the Memory Toolbox Test, a questionnaire assessing the knowledge of memory strategies.
Time frame: PRE (within 12 weeks before intervention starts) + POST-1 (within 8 weeks after the end of intervention) + POST-2 (2 years from PRE, +/- 3 months)
Plan to share: No
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Centre de Recherche de l'Institut Universitaire de Geriatrie de Montreal