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Hydration clinical trials

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NCT ID: NCT06132763 Completed - Dental Caries Clinical Trials

Healthy Hydration Pilot in Elementary Schools

Start date: November 9, 2023
Phase: N/A
Study type: Interventional

This study will pilot a school-based stakeholder-informed hydration intervention and examine its feasibility and preliminary efficacy.

NCT ID: NCT05510791 Completed - Hydration Clinical Trials

Impact of Nuun SPORT on Subjective Exercise Performance in Male and Female Runners

Start date: January 19, 2022
Phase: N/A
Study type: Interventional

The study will examine the impact of the Nuun Sport tablets, as compared to water only, on heart rate, perceived exertion, and related outcomes in male and female runners, during and following the performance of a 60-minute treadmill run.

NCT ID: NCT05451446 Completed - Dehydration Clinical Trials

The Effect of Proprietary Water on Physiological and Perceptual Responses

Start date: July 15, 2022
Phase: N/A
Study type: Interventional

The purpose of this study is to determine if drinking proprietary water (PW) during a standardized daily plan as compared to distilled water (control) and carbohydrate-electrolyte (CE) drink can improve hydration status over time. Another purpose is to determine if PW, as compared to control and CE, can improve hydration status, perceptual responses, physiological responses, and cognition measures in a heat stressful environment. Healthy, physically active males and females aged 18 to 50y will be recruited for the study. Participants will be randomized into one of three groups: PW, CE, or Control. The participant will be given a daily standardized plan integrating their assigned fluid into daily hydration habits for five days. Participants will provide their first-morning urine sample, keep a daily food log, and answer questions about their perceptions of hydration. After the five days, they will participate in a treadmill exercise protocol within a warm environment (heat chamber). Multiple physiological, perceptual, and cognitive measures will be obtained while participants exercise and then recover.

NCT ID: NCT05352724 Completed - Microbiota Clinical Trials

Clinical Trial to Evaluate the Efficacy of a Sport Drink After High-intensity Aerobic Exercise

Start date: October 20, 2022
Phase: N/A
Study type: Interventional

Although the general effectiveness of carbohydrate/electrolyte-based functional sports drinks on rehydration, recovery and sports performance has been widely demonstrated, there is controversy about the amounts, proportions and components that ensure the effectiveness of these products. The present study intends to analyze the specific effects of the beverages to be studied on these parameters, taking into account their particular formulation. Advances in research have allowed us to understand the importance of the intestinal microbiota on health, recovery and performance in sports. The consumption of functional drinks based on carbohydrates and electrolytes as supplementation is a constant in sports environments, with multiple studies on their properties, tolerance, safety and efficacy. However, there are no studies that analyze the effects of consuming these beverages and their interaction with the intestinal microbiota. Therefore, in addition, it is intended to evaluate the changes in the microbiota, through analysis of stool samples, during the sustained consumption of the beverages under study.

NCT ID: NCT05272540 Completed - Clinical trials for Postoperative Complications

Changes in Body Water During Surgery

Start date: September 13, 2016
Phase:
Study type: Observational

Fluid is added during anesthesia and surgery to maintain and balance the dynamic hemodynamics during a surgical procedure. Excess fluid after surgery is strongly correlated with morbidity and mortality. Bioelectrical impedance analysis (BIA) measures the total body water. Increased knowledge of the degree of preoperative hydration and the perioperative course can contribute to active treatment and reduced morbidity. Women and men ≥18 years of age who are to undergo gynecological or urological operations are included in the study. The purpose is to analyze the baseline status of the degree of hydration measured as the total body water and its components, and to monitor changes in these during a postoperative course, and to look for connections between these parameters and patient characteristics, laboratory data, type of surgery, type of anesthesia, care period and onset of postoperative symptoms and complications.

NCT ID: NCT05111392 Completed - Dehydration Clinical Trials

Hydration Dynamics and Influence of Beverage Composition

Start date: September 3, 2021
Phase: Phase 1/Phase 2
Study type: Interventional

The study examines interactions between fluid availability in the gut and fluid retention in the body. The relative rate of fluid uptake, the expansion of the plasma volume, and percent of fluid retained by the body will be measured in response to ingestion of beverages of different composition. Healthy, euhydrated adults will be studied. The results will help establish formulations of beverages that sustain if not promote acute euhydration.

NCT ID: NCT04764565 Completed - Hydration Clinical Trials

Impact of Nuun Instant on Hydration Status in Active Men and Women

Start date: February 23, 2021
Phase: N/A
Study type: Interventional

While Nuun Instant is commercially available and has received positive reviews from athletes, there have been no studies to date to evaluate the impact of this product on hydration status. Therefore, the purpose of this study is to determine the impact of Nuun Instant powder and new product under development called Nuun Electrolyte on hydration status in young and active men and women. We will follow a similar approach as used by Maughan and colleagues (2016) to measure the fluid balance (the difference between the amount of water consumed and passed as urine) and beverage hydration index (the relative amount of urine passed after consumption of a drink compared to water), while also measuring plasma volume using the method of Dill and Costill (1974).

NCT ID: NCT04460846 Completed - Hydration Clinical Trials

Evaluation of Hydration Status When Consuming Alkaline Water Compared to Reverse Osmosis Purified Water.

Start date: March 1, 2020
Phase: N/A
Study type: Interventional

To conduct a randomized, double-blinded, placebo-controlled, cross-over trial in a population of chronically, moderately dehydrated people comparing two waters on hydration status.

NCT ID: NCT04422158 Completed - Hydration Clinical Trials

Impact of Nuun Electrolyte Tablets on Hydration Status in Active Men and Women

Start date: June 3, 2020
Phase: N/A
Study type: Interventional

The purpose of this study is to determine the impact of Nuun electrolyte tablets on hydration status in young and active men and women. We will follow a similar approach as used by Maughan and colleagues (2016) to measure the beverage hydration index (the relative amount of urine passed after consumption of a drink compared to water). It is hypothesized that Nuun electrolyte tablets will result in a greater hydration status as compared to water only. Due to the fact that athletes use Nuun tablets at varying dosages, we will evaluate Nuun at both a single dosage and a double dosage. We maintain a non-directional hypothesis regarding the potential differences between the two different dosages tested.

NCT ID: NCT04012372 Completed - Hydration Clinical Trials

ROSA Oligomineral Water for Oral Hydration in 6-Month-Old Healthy Infants

ROSAH
Start date: July 20, 2019
Phase: N/A
Study type: Interventional

The present study evaluates the safety of ROSA oligomineral water in 6-to-12-month old healthy children.