Purpose

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.

Conditions

Eligibility

Eligible Ages
Between 18 Years and 30 Years
Eligible Sex
All
Accepts Healthy Volunteers
Yes

Inclusion Criteria

Individuals will be included: - SMU or Baylor University students - Ages of 18-30 years old.

Exclusion Criteria

  • Active smokers - Smoking cannabis or vape - Students with clinically significant asthma - COPD and emphysema - Allergic rhinitis - High levels of exhaled nitric oxide (FENO ≥40ppb) - Developing kidney stone - Clinically significant heart disease - Cerebrovascular disease - Thyroid dysfunction - Out-of-control diabetes - Significant current problems with schizophrenia, psychosis, mood disorders, suicidality, and drug or alcohol dependence or abuse

Study Design

Phase
Phase 2
Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel Assignment
Intervention Model Description
Double blinded, placebo controlled study
Primary Purpose
Prevention
Masking
Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)
Masking Description
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.

Arm Groups

ArmDescriptionAssigned Intervention
Experimental
Two active doses of beetroot juice
2 active (nitrate containing) doses of Beet-it Pro 400
  • Dietary Supplement: Beetroot juice
    Participants will take on dose in the morning and one in the afternoon, for 7 days during their final academic examinations
    Other names:
    • Beet-it 400
Active Comparator
One active dose of beetroot juice and one placebo dose of beetroot juice
1 active (nitrate containing) dose of Beet-it Pro 400 and one placebo (nitrate-depleted) dose of beetroot juice
  • Dietary Supplement: Beetroot juice
    Participants will take on dose in the morning and one in the afternoon, for 7 days during their final academic examinations
    Other names:
    • Beet-it 400
Placebo Comparator
Two placebo doses of beetroot juice
2 placebo (nitrate-depleted) doses of beetroot juice
  • Dietary Supplement: Beetroot juice
    Participants will take on dose in the morning and one in the afternoon, for 7 days during their final academic examinations
    Other names:
    • Beet-it 400

Recruiting Locations

Southern Methodist University
Dallas, Texas 75206
Contact:
Savannah Springfield, BA
214-768-6441
sspringfield@smu.edu

Baylor University
Waco, Texas 76796
Contact:
Danielle Young, Ph.D.
254-710-2236
Danielle_Young@baylor.edu

More Details

NCT ID
NCT06416228
Status
Recruiting
Sponsor
Southern Methodist University

Study Contact

Savannah Springfield, BA
(214) 768-6441
sspringfield@mail.smu.edu

Detailed Description

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).

Notice

Study information shown on this site is derived from ClinicalTrials.gov (a public registry operated by the National Institutes of Health). The listing of studies provided is not certain to be all studies for which you might be eligible. Furthermore, study eligibility requirements can be difficult to understand and may change over time, so it is wise to speak with your medical care provider and individual research study teams when making decisions related to participation.