Actively Recruiting
The VESPA Pilot Study
Led by Wake Forest University · Updated on 2025-07-16
30
Participants Needed
1
Research Sites
314 weeks
Total Duration
On this page
Sponsors
W
Wake Forest University
Lead Sponsor
W
Wells Fargo Faculty Scholar Endowment
Collaborating Sponsor
AI-Summary
What this Trial Is About
Physical activity has been described by the US federal government as a 'best buy' for public health. Unfortunately, most adults in the United States are not sufficiently active, and this worsens with age. Low levels of participation are driven by many challenging barriers, including lack of access, few opportunities for enjoyable activity, and few supportive social relationships, which is especially important given the central role of social connection for lasting behavior change. A half-century of research in behavioral sciences has generated effective group-based physical activity programs, but these are inaccessible to most as they are often delivered in a few select research centers. Recent advances in telehealth have offered media for extending these interventions more broadly, but the experience of such programs is often hampered by technology that does not allow for a sense of physical and social presence. Fortunately, uptake of virtual reality (VR) is increasing rapidly, and the medium has a high level of potential for advancing the delivery of immersive evidence-based group interventions to those that most need it. Thus our specific aims are: Specific aim 1: To test the feasibility and acceptability of a group-mediated physical activity intervention delivered fully via modern VR to older adults. Specific aim 2: To examine the impact of this program on overall physical activity among older adults compared to the current standard-of-care for telehealth: the video conference meeting platform.
CONDITIONS
Official Title
The VESPA Pilot Study
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Age of 45-80 years
- Body mass index between 30-45 kg/m2
- Low-active (30 or more minutes of moderate intensity physical activity on 2 or fewer days per week)
- Have access to home Wi-Fi
- Have regular access to a computer, tablet, or smartphone to receive teleconferencing calls
- Have a clear "VR space" (7'x7' object-free space)
- Have an "Activity buddy" (spouse, child, caregiver, etc.)
- Modified Telephone Interview for Cognitive Status (TICS-M) score of 32 or greater
- Consent from a physician for study participation
- Proficient in the English language
- Willingness to create or use existing personal Facebook account for virtual reality activities.
You will not qualify if you...
- Current involvement in other physical activity research studies
- Hearing or sight impairments that cannot be corrected and prevent telephone use or normal conversation, including colorblindness
- Dependence on a cane or walker
- More than 1 fall in the past year
- Contraindication to exercise
- Current or recent history (last 6 months) of symptomatic coronary heart disease, cancer, liver or kidney disease, severe lung disease, major physical impairment, or uncontrolled high blood pressure
- Myocardial infarction or cardiovascular procedure within last 3 months
- History or diagnosis of photosensitive epilepsy
- Score of "severe" on any question in the Virtual Reality Sickness Questionnaire
- Unwillingness to use a head-mounted virtual reality system
- Current severe or untreated depression
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Wake Forest University
Winston-Salem, North Carolina, United States, 27109
Actively Recruiting
Research Team
K
Kyle Kershner, BS
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
PREVENTION
Number of Arms
2
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