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Water Consumption, Hydration and Resting Energy Expenditure

Water Consumption, Hydration and Resting Energy Expenditure

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03258775
Enrollment
16
Registered
2017-08-23
Start date
2015-10-01
Completion date
2016-08-01
Last updated
2017-08-23

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Hydration and Resting Metabolism

Keywords

RMR, hydration, substrate oxidation

Brief summary

A randomized, cross over study will assess the effects of ingestion of high and low volumes of water on REE over 90 minutes. The high volume of water 500ml and the low volume of water 250ml. Participants will be computer randomized to determine which volume of water to receive first. Participants will arrive at the Nutrition Assessment Laboratory between 7:00 and 7:30am following a 9 hour overnight fast. Participants will be instructed not to consume any food or drink after 10pm the night before the assessment. Participants will also be asked to abstain from alcohol and caffeine for 3 days before the assessment. After verification of eligibility, baseline REE will be measured for 30 minutes followed by administration of first assigned dose of water. REE will be monitored for the next 90 minutes. Blood pressure and heart rate will also be monitored, simultaneously to REE. After a 7-10 day washout period, participants will return for their second test day where the second dose of water will be administered. A 7-10 day washout period was selected to allow participants time to resume normal diet and hydration between visits.

Interventions

After an overnight fast participants' RMR will be measured by indirect calorimetry for 30 minutes after which either a low (250ml) or high (500ml) dose of water will be consumed followed by an additional 90 minutes of indirect calorimetry. The test day will be repeated after 7-10 days with the second dose of water. The order in which the dose of water will be consumed will be randomized

Sponsors

George Mason University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
PREVENTION
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 39 Years
Healthy volunteers
Yes

Inclusion criteria

* 18-39 years of age * Generally Healthy men and women * BMI 18.5-28 * Willing to abstain from caffeine for 3 days prior to testing * Able to provide written consent in English * Ability to communicate in English (oral and written

Exclusion criteria

* \<18 or \>39 years * BMI \< 18.5 or \>28 * Pregnant or Nursing * Taking prescribed or over the counter medication affecting fluid balance or metabolism * Suffers from hepatic, renal, pulmonary, endocrine or hematological disease * Performs more than 3 hours a week of strenuous exercise * Consumes, on average, more than 2 alcoholic beverages per day * More than 5kg of weight change over the past 6 months * Claustrophobic

Design outcomes

Primary

MeasureTime frameDescription
Resting Metabolic Rate (RMR)90 minutesResting Metabolic Rate after water intake
Substrate oxidation90 minutesChange in substrate oxidation after water intake

Secondary

MeasureTime frame
blood pressure90 minutes
heart rate90 minutes

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026