NCT02205710

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.

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
99

participants targeted

Target at P50-P75 for not_applicable

Timeline
Completed

Started Aug 2016

Typical duration for not_applicable

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

July 29, 2014

Completed
2 days until next milestone

First Posted

Study publicly available on registry

July 31, 2014

Completed
2 years until next milestone

Study Start

First participant enrolled

August 1, 2016

Completed
2 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

August 1, 2018

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

August 1, 2018

Completed
Last Updated

August 2, 2019

Status Verified

August 1, 2017

Enrollment Period

2 years

First QC Date

July 29, 2014

Last Update Submit

July 31, 2019

Conditions

Outcome Measures

Primary Outcomes (3)

  • Change in ratings on cognitive training survey

    This survey aims to assess participant perceptions on cognitive training, and includes a series of related questions, rated on a scale of 1-7.

    Baseline, week 5

  • Change in neural activity

    We will measure resting state as well as task-related EEG responses to determine the effects of cognitive training at the neural level.

    Baseline, week 5

  • Change in performance on neuropsychological tests

    Using a set of standard neuropsychological evaluations, we will measure changes in attention, memory, and executive function following cognitive training.

    Baseline, week 5

Secondary Outcomes (1)

  • Change in ratings of psychological wellbeing

    Baseline, week 5

Study Arms (2)

Computerized cognitive training

EXPERIMENTAL

Series of gamified tasks.

Other: Computerized cognitive training

Computerized game training

PLACEBO COMPARATOR

Series of gamified tasks.

Other: Computerized games

Interventions

Also known as: Activate
Computerized cognitive training
Computerized game training

Eligibility Criteria

Age60 Years+
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • 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.

You may not qualify if:

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

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Bruyere Continuing Care

Ottawa, Ontario, K1N 5C8, Canada

Location

MeSH Terms

Conditions

Cognitive DysfunctionAlzheimer Disease

Condition Hierarchy (Ancestors)

Cognition DisordersNeurocognitive DisordersMental DisordersDementiaBrain DiseasesCentral Nervous System DiseasesNervous System DiseasesTauopathiesNeurodegenerative Diseases

Study Officials

  • Patrick Davidson, PhD

    University of Ottawa

    PRINCIPAL INVESTIGATOR
  • Sheida Rabipour, MSc

    University of Ottawa

    STUDY DIRECTOR

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
TRIPLE
Who Masked
PARTICIPANT, INVESTIGATOR, OUTCOMES ASSESSOR
Purpose
OTHER
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

July 29, 2014

First Posted

July 31, 2014

Study Start

August 1, 2016

Primary Completion

August 1, 2018

Study Completion

August 1, 2018

Last Updated

August 2, 2019

Record last verified: 2017-08

Locations