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VR Stimulation of Exercise Response in Sedentary Humans

VR Stimulation of Exercise Response in Sedentary Humans

Status
Recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07296991
Enrollment
48
Registered
2025-12-22
Start date
2025-09-30
Completion date
2028-08-31
Last updated
2025-12-23

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Metabolic Syndrome, Prolonged Inactivity

Keywords

Exercise, metabolic syndrome, insulin resistance, virtual reality

Brief summary

Prolonged sedentary conditions contribute to declining health across human populations and cause significant secondary health consequences for many patients whose illnesses or injuries prevent them from exercising. The investigators have demonstrated that in a small animal fruit fly model, genetic stimulation of neurons that promote adrenergic signaling is sufficient to mimic the benefits of exercise training even in sedentary animals. The investigator's pilot work in humans has confirmed that humans respond to Virtual Reality (VR) stimuli that mimic exercise by increasing heart rate and altering heart rate variability in a way consistent with increased adrenergic activity. In this study, the investigators will directly test for the first time whether repeated, controlled exposure to VR stimuli that induce adrenergic activity in sedentary humans can produce adaptive changes to protein expression and endurance performance like those produced by actual exercise in pre-diabetic participants with/without hypertension.

Interventions

BEHAVIORAL20 minutes cycling exercise

20 minutes cycling exercise

BEHAVIORALVirtual Reality

20 minutes virtual cycling

Sponsors

National Institute on Aging (NIA)
CollaboratorNIH
Wayne State University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
25 Years to 40 Years
Healthy volunteers
No

Inclusion criteria

1. Equal numbers male and female (32 each) 2. Blood glucose HbA1C: 5.7-6.4% or 100-125 mg/dL 3. BP: systolic\<120 and diastolic\<80 mmHg, systolic 120-129 mmHg and diastolic \<80 mmHg, or systolic \>130 mmHg and diastolic \>80 mmHg

Exclusion criteria

1. BMI\>35kg/m2 2. Currently involved in an exercise program or similar activity 3. Taking medications that could affect results, including beta-blockers or SSRIs 4. Demonstrate any form of discomfort with the VR experience through self-reported feelings of anxiety or nausea 5. Alcohol consumption above a minimal level(\<2 oz/night) 6. BP: Systolic \>160 mmHg and Diastolic \>110 mmHg

Design outcomes

Primary

MeasureTime frameDescription
Blood Glucose, HbA1C10 weeksPre-diabetic patients (Blood glucose 100-125 mg/dL, AbA1C 5.7-6.4%) may see improvement in values post-intervention

Secondary

MeasureTime frameDescription
10 minute walk time10 weeksdistance walked in 10 minutes is recorded pre- and post- intervention and may improve

Countries

United States

Contacts

Primary ContactAlyson Sujkowski, PhD
asujkows@med.wayne.edu419-461-4317
Backup ContactRobert J Wessells, PhD
7344764325

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026