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| Name | Class |
|---|---|
| Baylor University | OTHER |
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Currently, there is a lack of evidence-based prevention strategies for respiratory infection and management of these conditions can be costly to the public. Airway nitric oxide provides a first line of defense against pathogens, and beetroot juice, a source of dietary nitrate, has been shown to elevate nitric oxide. The main objective of this project is to demonstrate that one week of supplementation with beetroot juice elevates airway nitric oxide during stressful periods in young adults and thereby can protect against respiratory viral infections.
Study Title Beetroot Juice Supplement for Boosting Mucosal Immunity: The NO Cold Study
Objectives Aim 1: Demonstrate that a 7-day trial of daily beetroot juice or nitrate depleted placebo beetroot juice is feasible with acceptable retention and adherence during a period of real-life stress, using adherence monitoring of beetroot juice intake by cell phone recorded video; acceptable burdensomeness for participants and success of team coordination and study logistics should also be demonstrated.
Aim 2: Generate initial estimates of effect size for a) elevations in exhaled nitric oxide (FENO) and b) the correlation between changes in FENO and both infection reduction and cold symptom reduction (biological signature).
Aim 3: a) Examine if 2 daily doses of beetroot juice are more potent than 1 daily dose in elevating FENO, and b) investigate whether each beetroot juice dosage (1 dose and 2 doses) increases FENO more than the placebo.
Exploratory aims: Explore sex as a moderator of all the Aims. Also explore effects of competitors/inhibitors of NO (arginase, asymmetric dimethylarginine) in a) reducing FENO under stress, and b) whether beetroot juice buffers any of these potential adverse effects on FENO; c) investigate whether effects of stress cortisol, which negatively impact NO, cold symptoms, and respiratory infections, are also buffered by beetroot juice.
Design and Outcomes This is a double-blind, placebo controlled clinical trial to test the efficacy of beetroot juice as elevating airway NO, which is associated with reduced cold symptoms and respiratory viral infection rates, in undergraduate students aged 18-30.
Interventions and Duration Participants will be receiving 1 active daily dose of beetroot juice and 1 dose of nitrate-depleted placebo beetroot juice, 2 active daily doses of beetroot juice, or 2 daily doses of nitrate-depleted placebo beetroot.
Cold symptoms will be explored by questionnaire at baseline (in a low stress period during the semester) and subsequently twice during the final exam period, once at an early stage of the finals (days 1-3 of the final exam period), and once at a later stage (days 4-6). A follow-up online questionnaire packet will be administered 3 days after the last final day. FENO, sampling for viral PCR, salivary cortisol, and exhaled breath condensate will be undertaken at baseline, early finals, and late finals (in-person assessments are not feasible at follow-up, because students leave campus after finals).
Sample Size and Population The sample size is 150 students (n=66 at SMU site, n=84 at Baylor site). Female and male students 18-30 years old will be recruited from Baylor and SMU. The investigators will make an extra effort to guarantee equal representation of both genders. Participants can be from any ethnic or cultural background, as long as they can understand and read English adequately. The student population of both universities combined is diverse (28.5-38.5% minorities).
The investigators will stratify by sex and by site, to randomize participants to receiving 1 active daily dose of beetroot juice and 1 dose of nitrate-depleted placebo beetroot juice, 2 active daily doses of beetroot juice, or 2 daily doses of nitrate-depleted placebo beetroot juice (n=50 per group).
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Two active doses of beetroot juice | Experimental | 2 active (nitrate containing) doses of Beet-it Pro 400 |
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| One active dose of beetroot juice and one placebo dose of beetroot juice | Active Comparator | 1 active (nitrate containing) dose of Beet-it Pro 400 and one placebo (nitrate-depleted) dose of beetroot juice |
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| Two placebo doses of beetroot juice | Placebo Comparator | 2 placebo (nitrate-depleted) doses of beetroot juice |
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| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Beetroot juice | Dietary Supplement | Participants will take on dose in the morning and one in the afternoon, for 7 days during their final academic examinations |
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| Measure | Description | Time Frame |
|---|---|---|
| Exhaled Nitric Oxide | The Fraction of NO in Exhaled Breath (FENO, in ppb) will be measured with an electrochemical gas analyzer (NIOX vero). | Baseline (non-stress mid point of semester), 1-3 days into active beetroot shots (during final examination period), 4-6 days into active beetroot shots (during final examination period) |
| Viral Polymerase Chain Reaction | Binary positive/negative test results for a panel of viral and bacterial respiratory pathogens. | Baseline (non-stress mid point of semester), 4-6 days into active beetroot shots (during final examination period) |
| Wisconsin Upper Respiratory Symptom Survey (WURSS) | Assess symptoms of acute upper respiratory tract infections (common cold symptoms) by questionnaire | Baseline (non-stress mid point of semester), 1-3 days into active beetroot shots (during final examination period), 4-6 days into active beetroot shots (during final examination period), 1-3 days after finishing beetroot shots (after final examinations) |
| Adherence monitoring (feasibility) | Participants will upload a cell phone video of their intake for that day to a secure cloud folder, time stamp in comparison to assigned intake windows provides measure of adherence | Every day during active beetroot shots (Days 1-7) |
| Burdensomeness | Follow-up questionnaire will be administered with the online follow-up survey. It explores experience with the best mode of reminder receipt (email or text message), whether the participants guessed their condition, and how burdensome 8 aspects of the study (including daily intake, video recording, upload, questionnaires, physiological assessment) were. | 1-3 days after finishing beetroot shots (after final examinations) |
| Measure | Description | Time Frame |
|---|---|---|
| Acute stress | Ad-hoc acute stress rating | Baseline (non-stress mid point of semester), 1-3 days into active beetroot shots (during final examination period), 4-6 days into active beetroot shots (during final examination period), 1-3 days after finishing beetroot shots (after final examinations) |
| Cortisol |
| Measure | Description | Time Frame |
|---|---|---|
| One-day Food Record | One-day food record via the Automated Self-Administered 24-Hour platform; control variable | Baseline (non-stress mid point of semester), 1-3 days into active beetroot shots (during final examination period), 4-6 days into active beetroot shots (during final examination period) |
| Arginase |
Inclusion Criteria:
Individuals will be included:
Exclusion Criteria:
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| Name | Role | Phone | Extension | |
|---|---|---|---|---|
| Savannah Springfield, BA | Contact | (214) 768-6441 | sspringfield@mail.smu.edu | |
| Danielle Young, Ph.D. | Contact | (254) 710-2236 | Danielle_Young@baylor.edu |
| Name | Affiliation | Role |
|---|---|---|
| Thomas Ritz, Ph.D. | Southern Methodist University | Principal Investigator |
| Annie Ginty, Ph.D. | Baylor University | Study Director |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Southern Methodist University | Recruiting | Dallas | Texas | 75206 | United States |
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| ID | Term |
|---|---|
| D012141 | Respiratory Tract Infections |
| ID | Term |
|---|---|
| D007239 | Infections |
| D012140 | Respiratory Tract Diseases |
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Double blinded, placebo controlled study
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Both participating students and assessors will be blinded to the participants' group assignment. Since students and research staff will not know whether their beetroot juice is depleted or not, treatment conditions are double-blinded (juice "shots" will be pre-labeled by study statistician with a participant number based on the pre-study randomization, so neither the staff nor the participant know the contents). Students will also be assured of full blinding of course instructors, including the PIs and Co-Is, to names of study participants.
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Cortisol, from saliva sampled with passive drool test |
| Baseline (non-stress mid point of semester), 1-3 days into active beetroot shots (during final examination period), 4-6 days into active beetroot shots (during final examination period) |
| Perceived stress | Perceived Stress Scale (PSS) | Baseline (non-stress mid point of semester), 4-6 days into active beetroot shots (during final examination period) |
| Mood | Hospital Anxiety and Depression Scale (HADS) | Baseline (non-stress mid point of semester), 4-6 days into active beetroot shots (during final examination period) |
| Blood pressure (systolic and diastolic blood pressure) and heart rate | Measured after at least 10 min of acclimatization to the laboratory | Baseline (non-stress mid point of semester), 1-3 days into active beetroot shots (during final examination period), 4-6 days into active beetroot shots (during final examination period) |
From Exhaled breath condensate or saliva, competitors/inhibitor of NO; exploratory mediator of FENO |
| Baseline (non-stress mid point of semester), 1-3 days into active beetroot shots (during final examination period), 4-6 days into active beetroot shots (during final examination period) |
| Asymmetric dimethylarginine | From Exhaled breath condensate or saliva, competitors/inhibitor of NO; exploratory mediator of FENO | Baseline (non-stress mid point of semester), 1-3 days into active beetroot shots (during final examination period), 4-6 days into active beetroot shots (during final examination period) |
| Baylor University | Recruiting | Waco | Texas | 76796 | United States |
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