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Personalized tablet activities may boost brain training in seniors with mild cognitive impairment
NCT ID NCT03292705
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study tested whether a personalized computer program (PEP) could improve attitudes toward technology and engagement with cognitive training in 49 older adults with mild cognitive impairment living in senior communities. Participants first used PEP or a control activity for 4 weeks, then all completed 6 weeks of standard cognitive training. The goal was to see if personalized, enjoyable computer use could make subsequent brain training more effective.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Personalized Engagement Program (PEP) – a tablet-based system with tailored leisure activities
- What this could lead to
- If it works, this approach could make cognitive training more engaging and effective for older adults with mild memory problems.
- What could go wrong
- This is a small, early proof-of-concept study with only 49 participants. Results may not apply to everyone, and the benefits may be modest.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
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Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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49 people
The number who actually took part.
- Started
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Oct 2017
- Finished
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Sep 2019
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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60 years and older
- Sex
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Anyone
- Healthy volunteers
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Accepted
You do not need to have the condition being studied to take part.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * 18 ≤ MoCA ≤ 26 * RAVLT Delayed Recall Total Score ≤ 6 (or 1.5 SD below age-corrected norms) * mild or no active depressive symptoms * intact or mild deficits in IADL functioning * if on AD medication (i.e., Memantine or cholinesterase inhibitors), antidepressant, or anxiolytics, no changes of doses in the 3 months prior to recruitment; * age ≥60 years * English-speaking * adequate visual and hearing acuity for testing * intact decision making capacity. Exclusion Criteria: * current enrollment in another cognitive improvement study; * uncontrollable major depression: or other psychopathology identified by staff or medical records; * having active legal guardian (indicating impaired capacity for decision making); * medical history of AD or other types of dementia
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
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Brickstone/Saint John Meadow
Rochester, New York, 14618, United States
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River Edge Manor
Rochester, New York, 14642, United States
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