- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07468539
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
Status
Completed
Conditions
Intervention / Treatment
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
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-
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Nottingham, United Kingdom, NG11 8NS
- Nottingham Trent University, Clifton Campus
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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
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Consumption of a water volume (from water) equal to 150% of body mass loses from exercise-induced hypohydration
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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
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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
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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
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([post-exercise body mass (kg) - Pre-exercise body mass (kg)] x 1000) + water volume consumed (g) - cumulative urine output during rehydration period (g)
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Baseline (pre-exercise), post-exercise, and 0, 1, 2, 3, and 4 h post-rehydration
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Cumulative urine volume
Time Frame: 0, 1, 2, 3, and 4 h post-rehydration
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0, 1, 2, 3, and 4 h post-rehydration
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|
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Total urine volume
Time Frame: Sum of urine produced at 0, 1, 2, 3, and 4 h post-rehydration
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Total urine volume produced during the rehydration period
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Sum of urine produced at 0, 1, 2, 3, and 4 h post-rehydration
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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
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Blood glucose area under the curve
Time Frame: The 2h period following rehydration
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The 2h period following rehydration
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Hyperglycaemia incidence
Time Frame: The 2 h period following rehydration
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Number of participants that experience blood glucose > 7.8 mmol/L
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The 2 h period following rehydration
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Hypoglycaemia incidence
Time Frame: The 2 h period following rehydration
|
The number of participants that experience blood glucose < 3.9 mmol/L
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The 2 h period following rehydration
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Urine osmolality
Time Frame: Baseline (pre-exercise), post-exercise, and 0, 1, 2, 3, and 4 h post-rehydration
|
A measure of urine concentration.
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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.
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Baseline (pre-exercise) and post-exercise (approximately 2 h post-baseline, depending on sweat losses during cycling in the heat)
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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
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Participants asked to rate their thirst on a scale of 0-10 (0 = no symptom, 10 = maximum symptom)
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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
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Gastrointestinal comfort
Time Frame: Baseline (pre-exercise), post-exercise, and 0, 1, 2, 3, and 4 h post-rehydration
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Participants asked to rate their gastrointestinal comfort on a scale of 0-10 (0 = no symptom, 10 = maximum symptom)
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Baseline (pre-exercise), post-exercise, and 0, 1, 2, 3, and 4 h post-rehydration
|
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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.
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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.
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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.
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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.
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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.
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Time in environmental chamber
Time Frame: Up to 120 minutes, depending on body mass losses during cycling in the heat
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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.
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Up to 120 minutes, depending on body mass losses during cycling in the heat
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Laboratory temperature
Time Frame: Baseline (pre-exercise), post-exercise, and 0, 1, 2, 3, and 4 h post-rehydration
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Temperature (degrees Celsius) of the laboratory measured across the day and averaged.
Averages compared across trials.
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Baseline (pre-exercise), post-exercise, and 0, 1, 2, 3, and 4 h post-rehydration
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|
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.
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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
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Humidity (relative humidity) of the laboratory measured across the day and averaged.
Averages compared across trials.
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Baseline (pre-exercise), post-exercise, and 0, 1, 2, 3, and 4 h post-rehydration
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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.
Sponsor
Collaborators
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
Additional Relevant MeSH Terms
Other Study ID Numbers
- 1911625
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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