The Interactive Physical and Cognitive Exercise System
NCT03069391 · Status: UNKNOWN · Phase: NA · Type: INTERVENTIONAL · Enrollment: 31
Last updated 2020-03-31
Summary
This study is intended to clarify the benefits to brain health and thinking processes that result from different forms of exercise. In particular, this study will investigate the possible benefits of physical exercise (such as pedaling an under-table stationary elliptical) or mental exercise (such as playing a videogame on a portable tablet), or combining these activities together (as in the iPACES™ exergame).
Conditions
- Alzheimer Disease, Early Onset
- MCI
- Aging
- Mild Cognitive Impairment
- Neurocognitive Disorder
- Cognitive Impairment
- Cognitive Change
Interventions
- BEHAVIORAL
-
physical exercise alone (PES) first
following 2-week placebo for all participants, participants in this arm will then start their active intervention with a randomly assigned 2-week physical exercise-only intervention, then 2-week cognitive exercise-only intervention, then 2-week and 3 month intervals of iPACES™ (interactive physical and cognitive exercise)
- DEVICE
-
cognitive exercise alone (iCE) first
following 2-week placebo for all participants, participants in this arm will then start their active intervention with a randomly assigned 2-week cognitive exercise-only intervention, then 2-week physical exercise-only intervention, then 2-week and 3 month intervals of iPACES™ (interactive physical and cognitive exercise)
- DEVICE
-
interactive Physical and Cognitive Exercise (iPACES™)
following 2-week placebo for all participants, participants in this arm will then start their active intervention with a randomly assigned 2-week cognitive exercise-only intervention, then 2-week physical exercise-only intervention, then 2-week and 3 month intervals of iPACES™ (interactive physical and cognitive exercise)
Sponsors & Collaborators
-
1st Playable Productions
collaborator OTHER -
Albany Medical College
collaborator OTHER -
Skidmore College
collaborator OTHER -
University of Illinois at Urbana-Champaign
collaborator OTHER -
National Institute on Aging (NIA)
collaborator NIH -
Union College, New York
lead OTHER
Principal Investigators
-
Cay Anderson-Hanley, PhD · Union College
Study Design
- Allocation
- NON_RANDOMIZED
- Purpose
- TREATMENT
- Masking
- NONE
- Model
- CROSSOVER
Eligibility
- Min Age
- 50 Years
- Sex
- ALL
- Healthy Volunteers
- Yes
Timeline & Regulatory
- Start
- 2017-03-04
- Primary Completion
- 2022-06-30
- Completion
- 2022-06-30
- FDA Device
- Yes
Countries
- United States
Study Locations
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