Skip to main content
Clinical Trials/NCT04678778
NCT04678778CompletedNot Applicable

Targeted Physical and Cognitive Activity in a VR Environment - COVID-19 Protocol

University of Southern California1 site in 1 country14 target enrollmentStarted: March 19, 2019Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Enrollment
14
Locations
1
Primary Endpoint
Mnemonic Similarity Task for visual memory performance - discrimination index

Study Overview

Brief Summary

The overarching goal of this pilot clinical trial is to use a novel virtual reality (VR)-based intervention that simultaneously engages physical and cognitive activity aimed at improving brain and cognitive outcomes in older adults. Physical activity is a promising lifestyle intervention for mitigating cognitive decline or delaying onset of dementia. However, to fully leverage beneficial brain effects of physical activity, training the brain to learn and engage in a cognitively stimulating environment may be the key to enhanced brain and cognitive outcomes.

Study Design

Study Type
Interventional
Allocation
Na
Intervention Model
Single Group
Primary Purpose
Other
Masking
None

Eligibility Criteria

Ages
50 Years to 85 Years (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
Yes

Inclusion Criteria

  • •50-85 Years Old
  • •Able to Walk Without Assistance
  • •Fluent in English
  • •No Ferromagnetic Metal in Body
  • •Able to Participate in Moderate Aerobic Physical Activity

Exclusion Criteria

  • •Severe Brain Injury/ Head Trauma
  • •Pacemakers or Metal Implants
  • •Claustrophobia
  • •Contradictions to Magnetic Resonance Imaging (MRI)/ Positron Emission Tomography (PET) Brain Scans
  • •Opposition to Blood Draws

Arms & Interventions

Combined, simultaneous physical and cognitive activity

Experimental

The combined physical and cognitive activity VR arm will participate in our customized spatial navigation program that increases difficulty and length per trial over time. As described in the Game Design section, each session will consist of 5 trials. The first trial will be a long-delay free recall condition from the previous day's path. The next 4 trials will consist of learning, cued recall, and free recall. This VR-based spatial navigation program has been tested in our feasibility trial for safety and tolerability in older adults.

Intervention: Physical and Cognitive Activity (Behavioral)

Outcomes

Primary Outcomes

Mnemonic Similarity Task for visual memory performance - discrimination index

Time Frame: 12 weeks

With the study's primary focus on hippocampal function, we will use the Mnemonic Separation Task (MST), a hippocampus-dependent discrimination test of similar objects, as our primary cognitive outcome.

Magnetic Resonance Image (MRI) brain scan of hippocampal volume (cubic mm)

Time Frame: 12 weeks

The hippocampus has been shown to be a selectively vulnerable region in Alzheimer's Disease (AD), and several studies, including our own, identified a dysfunctional brain signal in the hippocampus in Mild Cognitive Impairment (MCI) patients. We propose to examine the effects of exercise on remediating this hyperactive signal exhibited in MCI patients.

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Judy Pa

Associate Professor of Neurology

University of Southern California

Study Sites (1)

Loading locations...

Similar Trials