Beetroot Juice for Boosting Immunity During a Time of Stress.
Beetroot Juice
+ Placebo Control
Basic Science Study
Summary
Study start date: April 11, 2022
Actual date on which the first participant was enrolled.This study investigates whether drinking beetroot juice can help boost immunity and improve overall well-being during stressful times, such as final exams for college students. Stress can lower nitric oxide levels in the body, which may affect immunity and heart health. By examining how beetroot juice impacts these factors, the study aims to determine if this dietary supplement can alleviate some of the physical and psychological effects of stress. The target group is healthy undergraduate students, as stress during exams is a common challenge with significant impact on their health and performance. Participants in the study are divided into two groups during their final exams. One group drinks beetroot juice twice a day for a week, while the other group receives a placebo drink, which has no active ingredients. Researchers monitor several health indicators, including cold symptoms, levels of a protein called IL-8, blood pressure, airway nitric oxide, and mood changes. These are measured through three laboratory visits, and participants complete a questionnaire after exams to evaluate symptoms. This study aims to see if beetroot juice can positively influence health markers during high-stress periods.
Protocol
This section provides details of the study plan, including how the study is designed and what the study is measuring.114 patients to be enrolled
Total number of participants that the clinical trial aims to recruit.Basic Science Study
Eligibility
Researchers look for people who fit a certain description, called eligibility criteria: person's general health condition or prior treatments.Any sex
Biological sex of participants that are eligible to enroll.From 18 to 40 Years
Range of ages for which participants are eligible to join.Healthy volunteers allowed
If individuals who are healthy and do not have the condition being studied can participate.Criteria
Study Plan
Find out more about all the medication administered in this study, their detailed description and what they involve.2 intervention groups are designated in this study
50% chance of being blinded to the placebo group
Treatment Groups
Group I
ExperimentalGroup II
PlaceboStudy Objectives
Primary Objectives
Secondary Objectives
Study Centers
These are the hospitals, clinics, or research facilities where the trial is being conducted. You can find the location closest to you and its status.This study has 2 locations
Annie T. Ginty
Waco, United States