Actively Recruiting

Phase Not Applicable
Age: 50Years - 85Years
All Genders
Healthy Volunteers
ID06124339

Interventions to Promote Brain Health Virtual Reality Study

Led by University of California, San Diego · Updated on 2024-07-10

150

Participants Needed

1

Research Sites

25 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Researchers are studying brain health and cognition in older adults aged 50 to 85 using a new virtual reality (VR) approach. This trial aims to compare three types of activities: physical exercise, VR-based cognitive tasks, and a combination of both, to better understand how these interventions affect brain health and memory. The study is sponsored by the University of California, San Diego, and focuses on aging-related cognitive changes and memory issues. Participants will engage in one of three programs over 16 weeks, each with three sessions per week. The physical activity group will cycle on a stationary bike for 20 to 50 minutes daily with varying difficulty. The VR cognitive activity involves a spatial navigation program that gradually becomes more challenging. The combined group will perform both the physical cycling and VR spatial navigation activities simultaneously. During the study, participants' memory performance will be evaluated, focusing on changes over the 16-week period. Researchers will monitor physical health and brain function through various assessments. The trial includes safety measures such as ensuring participants can safely ride a stationary bike and screening for conditions that might affect participation. Overall, the study seeks to understand how these different interventions may impact brain health in aging adults.

CONDITIONS

Brief Title

Brain Health Virtual Reality Study

Who Can Participate

Age: 50Years - 85Years
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • 50 to 85 years of age
  • Fluent in English
  • Can safely ride a stationary bike
Not Eligible

You will not qualify if you...

  • Dementia
  • History of a neurological disorder
  • Severe sensory deficits
  • Inability to perform intervention (e.g., inability to cycle safely)
  • Contraindications to MRI scan (e.g., pacemaker)
  • Fear of needles or blood
  • Prior history of fainting due to sight of needles or blood

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

Outpatient Treatment

Duration - 16 weeks

Participants engage in physical activity, cognitive activity (VR spatial navigation), or a combination of both as assigned. Sessions occur three times a week over 16 weeks.

Three sessions per week

Trial Site Locations

Total: 1 location

1

University of California, San Diego

San Diego, California, United States, 92122

Actively Recruiting

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Research Team

S

Study Coordinator

I

Isenberg

How is the study designed?

Study Type

INTERVENTIONAL

Masking

SINGLE

Allocation

RANDOMIZED

Model

FACTORIAL

Primary Purpose

PREVENTION

Number of Arms

3

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