Post-exercise Rehydration: A Randomised Cross-over Trial Comparing a 100% Fruit Beverage, a Glucose-based Sports Drink, and Water

March 9, 2026 updated by: Loris Juett, Nottingham Trent University

Comparing The Rehydration Properties Of Two Sports / Hydration Drinks And Water, Following Exercise In The Heat

It is well-established that exercise has many health benefits. During exercise in temperate/hot conditions, sweating is necessary to dissipate heat. This sweating typically results in dehydration, which may impair physical and mental performance. Therefore, following exercise, effective rehydration is important to restore an optimal hydration state and therefore physical and mental performance. If an individual only rehydrates with water, though, it is unlikely that they will fully rehydrate as plain water is not very well-retained by the body, due to its lack of carbohydrate and electrolytes. For this reason, sports/ hydration drinks are likely to aid in better rehydration, due to their carbohydrate and electrolyte content. This project aims to compare the rehydration effectiveness and glucose responses to two sports / hydration drinks and water (with different carbohydrate and electrolyte contents).

Study Overview

Study Type

Interventional

Enrollment (Actual)

17

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

      • Nottingham, United Kingdom, NG11 8NS
        • Nottingham Trent University, Clifton Campus

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

  • Adult

Accepts Healthy Volunteers

Yes

Description

Inclusion Criteria:

- Training/performing > 1 hrs a week

Exclusion Criteria:

  • Smoker.
  • Pregnant, attempting to become pregnant, or breastfeeding.
  • Diabetic.
  • You have adverse events/reactions in response to fingertip capillary blood sampling which includes, but is not limited to; fainting and/or serious bruising.
  • History of heat-related illness.
  • History of heart failure, pulmonary hypertension, embolism, or other pulmonary heart disease.
  • Previously diagnosed with COPD, emphysema, bronchitis or similar respiratory illness.
  • Have a history of severe allergic reactions.
  • History of kidney issues.
  • Regular use of non-steroidal anti-inflammatory medications.
  • Any other medical conditions / medications that may interfere with an individuals ability to safely perform exercise in the heat and experience dehydration.
  • Allergies/intolerances to any of the following ingredients: Glucose Syrup, Acid (Citric Acid), Acidity Regulator (Sodium Citrate), Extract of Black Carrot, Watermelon, pomegranate, lime, Preservatives (Potassium Sorbate, Dimethyl Dicarbonate), Stabilisers (Acacia Gum), Sweeteners (Aspartame, Acesulfame K), Antioxidant (Ascorbic Acid), Flavourings, Niacin (Vitamin B3).
  • Elite athlete subject to doping tests

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Basic Science
  • Allocation: Randomized
  • Interventional Model: Crossover Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Water
Consumption of a water volume (from water) equal to 150% of body mass loses from exercise-induced hypohydration
Consumption of a water volume (from water) equal to 150% of body mass loses from exercise-induced hypohydration
Experimental: Glucose-based sports drink
Consumption of a water volume (from a glucose-based sports drink) equal to 150% of body mass loses from exercise-induced hypohydration
Consumption of a water volume (from a glucose-based sports drink) equal to 150% of body mass loses from exercise-induced hypohydration
Experimental: Fruit beverage
Consumption of a water volume (from a fruit beverage) equal to 150% of body mass loses from exercise-induced hypohydration
Consumption of a water volume (from a fruit beverage) equal to 150% of body mass loses from exercise-induced hypohydration

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Net water Balance
Time Frame: Baseline (pre-exercise), post-exercise, and 0, 1, 2, 3, and 4 h post-rehydration
([post-exercise body mass (kg) - Pre-exercise body mass (kg)] x 1000) + water volume consumed (g) - cumulative urine output during rehydration period (g)
Baseline (pre-exercise), post-exercise, and 0, 1, 2, 3, and 4 h post-rehydration
Cumulative urine volume
Time Frame: 0, 1, 2, 3, and 4 h post-rehydration
0, 1, 2, 3, and 4 h post-rehydration
Total urine volume
Time Frame: Sum of urine produced at 0, 1, 2, 3, and 4 h post-rehydration
Total urine volume produced during the rehydration period
Sum of urine produced at 0, 1, 2, 3, and 4 h post-rehydration
Water retention
Time Frame: 4 h post-rehydration
([water volume consumed (g) - total urine volume produced during the rehydration period (g)] / water volume consumed (g)) x 100
4 h post-rehydration

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Blood glucose concentration
Time Frame: Baseline (pre-exercise), post-exercise, and 0, 0.25, 0.5, 0.75, 1, 1.5, and 2 h post-rehydration
Baseline (pre-exercise), post-exercise, and 0, 0.25, 0.5, 0.75, 1, 1.5, and 2 h post-rehydration
Blood glucose area under the curve
Time Frame: The 2h period following rehydration
The 2h period following rehydration
Hyperglycaemia incidence
Time Frame: The 2 h period following rehydration
Number of participants that experience blood glucose > 7.8 mmol/L
The 2 h period following rehydration
Hypoglycaemia incidence
Time Frame: The 2 h period following rehydration
The number of participants that experience blood glucose < 3.9 mmol/L
The 2 h period following rehydration
Urine osmolality
Time Frame: Baseline (pre-exercise), post-exercise, and 0, 1, 2, 3, and 4 h post-rehydration
A measure of urine concentration.
Baseline (pre-exercise), post-exercise, and 0, 1, 2, 3, and 4 h post-rehydration
Body mass
Time Frame: Baseline (pre-exercise) and post-exercise (approximately 2 h post-baseline, depending on sweat losses during cycling in the heat)
Body mass in kilograms at baseline compared across trials. Body mass loss (both in grams and as a percentage) from pre-exercise to post-exercise compared across trials.
Baseline (pre-exercise) and post-exercise (approximately 2 h post-baseline, depending on sweat losses during cycling in the heat)
Thirst
Time Frame: Baseline (pre-exercise), towards the end of each 10 minute block of exercise (cycling in the heat), post-exercise, and 0, 1, 2, 3, and 4 h post-rehydration
Participants asked to rate their thirst on a scale of 0-10 (0 = no symptom, 10 = maximum symptom)
Baseline (pre-exercise), towards the end of each 10 minute block of exercise (cycling in the heat), post-exercise, and 0, 1, 2, 3, and 4 h post-rehydration
Gastrointestinal comfort
Time Frame: Baseline (pre-exercise), post-exercise, and 0, 1, 2, 3, and 4 h post-rehydration
Participants asked to rate their gastrointestinal comfort on a scale of 0-10 (0 = no symptom, 10 = maximum symptom)
Baseline (pre-exercise), post-exercise, and 0, 1, 2, 3, and 4 h post-rehydration
Rating of perceived exertion (RPE)
Time Frame: Measured towards the end of each 10 minute block of exercise (cycling in the heat). Up to 8 blocks lasting a total of 120 minutes (10 minutes of cycling, followed by 5 minutes of rest), depending on body mass loss.
Participants asked to rate their RPE on a scale of 6-20. This is a measure of exercise intensity. Average taken for dehydration period. Average compared across trials.
Measured towards the end of each 10 minute block of exercise (cycling in the heat). Up to 8 blocks lasting a total of 120 minutes (10 minutes of cycling, followed by 5 minutes of rest), depending on body mass loss.
Thermal sensation
Time Frame: Measured towards the end of each 10 minute block of exercise (cycling in the heat). Up to 8 blocks lasting a total of 120 minutes (10 minutes of cycling, followed by 5 minutes of rest), depending on body mass loss.
Participants asked to rate their thermal sensation on a scale of -10 (unbearably cold) to 10 (unbearably hot). Average taken for dehydration period. Average compared across trials.
Measured towards the end of each 10 minute block of exercise (cycling in the heat). Up to 8 blocks lasting a total of 120 minutes (10 minutes of cycling, followed by 5 minutes of rest), depending on body mass loss.
Time in environmental chamber
Time Frame: Up to 120 minutes, depending on body mass losses during cycling in the heat
The time in minutes that the participant spent in the environmental chamber at 35 degrees Celsius, doing repeated blocks of 10 minutes of cycling followed by 5 minutes of rest, until they reached approximately 1.5% body mass loss. Time compared across trials.
Up to 120 minutes, depending on body mass losses during cycling in the heat
Laboratory temperature
Time Frame: Baseline (pre-exercise), post-exercise, and 0, 1, 2, 3, and 4 h post-rehydration
Temperature (degrees Celsius) of the laboratory measured across the day and averaged. Averages compared across trials.
Baseline (pre-exercise), post-exercise, and 0, 1, 2, 3, and 4 h post-rehydration
Environmental chamber temperature
Time Frame: Measured towards the end of each 10 minute block of exercise (cycling in the heat). Up to 8 blocks lasting a total of 120 minutes (10 minutes of cycling, followed by 5 minutes of rest), depending on body mass loss.
Environmental chamber temperature (degrees Celsius) measured and averaged for the cycling in the heat period of each participant. Averages compared across trials.
Measured towards the end of each 10 minute block of exercise (cycling in the heat). Up to 8 blocks lasting a total of 120 minutes (10 minutes of cycling, followed by 5 minutes of rest), depending on body mass loss.
Laboratory humidity
Time Frame: Baseline (pre-exercise), post-exercise, and 0, 1, 2, 3, and 4 h post-rehydration
Humidity (relative humidity) of the laboratory measured across the day and averaged. Averages compared across trials.
Baseline (pre-exercise), post-exercise, and 0, 1, 2, 3, and 4 h post-rehydration
Environmental chamber humidity
Time Frame: Measured towards the end of each 10 minute block of exercise (cycling in the heat). Up to 8 blocks lasting a total of 120 minutes (10 minutes of cycling, followed by 5 minutes of rest), depending on body mass loss.
Environmental chamber humidity (relative humidity) measured and averaged for the cycling in the heat period of each participant. Averages compared across trials.
Measured towards the end of each 10 minute block of exercise (cycling in the heat). Up to 8 blocks lasting a total of 120 minutes (10 minutes of cycling, followed by 5 minutes of rest), depending on body mass loss.

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

November 8, 2024

Primary Completion (Actual)

May 22, 2025

Study Completion (Actual)

May 22, 2025

Study Registration Dates

First Submitted

March 3, 2026

First Submitted That Met QC Criteria

March 9, 2026

First Posted (Actual)

March 12, 2026

Study Record Updates

Last Update Posted (Actual)

March 12, 2026

Last Update Submitted That Met QC Criteria

March 9, 2026

Last Verified

March 1, 2026

More Information

Terms related to this study

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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