Actively Recruiting
Does Vitamin C Increase the Body Heat Generated By The Nervous System?
Led by Colorado State University · Updated on 2026-01-14
20
Participants Needed
1
Research Sites
26 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
This trial studies adults aged 18 to 40 years with a body mass index indicating overweight to see if vitamin C can increase the heat produced by the sympathetic nervous system and raise vitamin D levels during nervous system activation. It aims to find out how much body temperature and circulating vitamin D change when beta-adrenergic receptors are stimulated with and without vitamin C. Participants visit the lab twice where beta-adrenergic receptors are stimulated using isoproterenol. One visit includes isoproterenol with saline only, and the other includes isoproterenol with saline and vitamin C. The order of these visits is randomized. Body temperature is measured with a thermometer and thermal camera, and blood samples are taken to measure vitamin D levels. During the study, participants undergo body temperature measurements and blood draws at baseline and after doses of isoproterenol at 30, 60, and 90 minutes. Researchers monitor changes in temperature and vitamin D concentration to assess the effect of vitamin C during stimulation. The total participation involves two lab visits with these assessments and monitoring under medical supervision.
CONDITIONS
Brief Title
Does Vitamin C Increase the Body Heat Generated By The Nervous System?
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Age 18-40 years (inclusive)
- Body mass index greater than or equal to 25 kg/m2 and less than 30 kg/m2
- Stable weight with no change greater than 5 pounds in the previous 6 months
- Willingness to abstain from caffeine and alcohol for 24 hours before study visits
- Competency in English to understand and communicate during the study
You will not qualify if you...
- History of autonomic, cardio-pulmonary, or metabolic diseases including heart failure, hypertension, arrhythmia, vascular disease, or diabetes
- Pregnancy or breastfeeding
- Habitual use of tobacco, nicotine products, or recreational drugs (2 or more uses in the past month)
- History of sulfite allergy
- Use of vitamin or antioxidant supplements in the previous 4 weeks such as vitamin C, vitamin E, or multivitamins
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
Duration - Two visits scheduled separately
Participants attend two lab visits where beta-adrenergic receptors are stimulated with isoproterenol. During one visit, isoproterenol is delivered with saline only, and during the other visit, it is delivered with saline and vitamin C. The order of visits is randomized. Body temperature and blood vitamin D levels are measured before and after dosing.
2 visits (in-person)
Trial Site Locations
Total: 1 location
1
Colorado State University
Fort Collins, Colorado, United States, 80523
Actively Recruiting
Research Team
C
Christopher Bell, PhD
T
Taylor Ewell, M.S.
How is the study designed?
Study Type
INTERVENTIONAL
Masking
SINGLE
Allocation
RANDOMIZED
Model
CROSSOVER
Primary Purpose
BASIC_SCIENCE
Number of Arms
2
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