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Not yet recruiting NCT06825962

The Effect of Hydration on Postprandial Metabolic Responses

No phase Interventional Glycaemia

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: Water intake, Water restriction.
Who it may be relevant to
Registry conditions: Glycaemia. Basic parameters: 18 years — 45 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
United Kingdom
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →

Overview

Certain populations, such as industrial workers and endurance athletes are particularly susceptible to dehydration due to exposure to heat for long periods of time causing evaporative water loss via sweating. The physical and cognitive decrements associated with dehydration have been widely researched, however the effect of dehydration on metabolism is lesser known. As climate change is causing temperatures to rise, and metabolic diseases such as type 2 diabetes are more common, the effect of dehydration on metabolism, specifically glycemic response to meals, needs to be established for future recommendations in clinical, environmental and athletic settings. Therefore, the aim of this study is to investigate the effect of acute exercise-induced dehydration on subsequent metabolic responses to feeding (i.e. glycaemia and insulinaemia).

Interventions

  • Other Water intake
    Water ingested to fully replace sweat losses during exercise.
  • Other Water restriction
    Water restriction to induce hypohydration of \~3% body mass through sweat losses during exercise.

Primary outcome measures

  • Plasma glucose [Time frame: 6 hours]
Secondary outcome measures (11)
  • Plasma insulin [Time frame: 6 hours]
  • Plasma osmolality [Time frame: 6 hours]
  • Plasma volume change [Time frame: 6 hours]
  • Urine volume [Time frame: 6 hours]
  • Body mass [Time frame: 6 hours]
  • Urine specific gravity/osmolality [Time frame: 6 hours]
  • Thirst sensation [Time frame: 6 hours]
  • Hunger sensation [Time frame: 6 hours]
  • Fullness sensation [Time frame: 6 hours]
  • Core body temperature [Time frame: 6 hours]
  • Blood pressure [Time frame: 6 hours]

Eligibility criteria

Inclusion criteria

  • Male or female
  • Generally fit and healthy
  • Participate in endurance or intermittent exercise at least 3 times a week or minimum of 150 minutes moderate intensity activity per week

Exclusion criteria

  • < 18 or > 45
  • Any health condition that may affect study outcomes (e.g., endocrine/liver/renal/cardiovascular disease)
  • Any morbidity that affects ability to cycle
  • Smoker or vaper

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: Yes

Study design

Allocation
Randomized
Model
Crossover
Masking
Open label
Primary purpose
Basic science

Study locations

United Kingdom · 1 center
  • Loughborough University — Loughborough

Identifiers

NCT: NCT06825962 · 2025-20370

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗