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The Effect of Proprietary Water on Physiological and Perceptual Responses

NCT05451446 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 47

Last updated 2023-04-11

No results posted yet for this study

Summary

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.

Conditions

Interventions

DIETARY_SUPPLEMENT

proprietary water

They are randomized to consume a proprietary water product for five-free living days and to drink on the heat stress chamber day.

OTHER

Active comparator

They are randomized to consume a carbohydrate drink for five-free living days and to drink on the heat stress chamber day.

OTHER

Placebo

They are randomized to consume water for five-free living days and to drink on the heat stress chamber day.

Sponsors & Collaborators

  • HydraVes Technologies Inc.

    collaborator UNKNOWN

  • University of South Carolina

    lead OTHER

Study Design

Allocation
RANDOMIZED
Purpose
OTHER
Masking
SINGLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
50 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2022-07-15
Primary Completion
2022-12-15
Completion
2023-04-05

Countries

  • United States

Study Locations

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Entities

Diseases

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT05451446 on ClinicalTrials.gov