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The Effect of Small Changes in Hydration on Cognition

How do Small Changes in Hydration Influence Cognition: A Mechanistic Investigation

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02671149
Enrollment
101
Registered
2016-02-02
Start date
2015-09-30
Completion date
2016-03-31
Last updated
2020-04-06

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

Conditions

Cognition, Hydration

Brief summary

The aim of this study is to determine whether drinking plain water when mildly dehydrated benefits cognitive performance and mood. Volunteers undergo a dehydration protocol designed to result in minor dehydration. While some participants receive two 150ml drinks of water others do not. Differences in cognitive functioning are assessed.

Detailed description

As an essential nutrient, an inadequate intake of water has negative consequences: without a source of water death will occur in days. When Benton and Young (2015) reviewed the topic they concluded that in healthy adults, mild dehydration (in the range of a loss of 2% body mass) had been found to adversely influence mood and cognition. However, it is unclear at what degree of hypohydration these effects begin to emerge. This study was designed to determine whether small changes in hydration, of the level that might occur on a day to day basis, influence cognition and mood. During a dehydration protocol (sitting in a room heated to 30 degrees for four hours) young adult participants receive either drink two 150ml cups of water or nothing. Effects on memory, attention and mood are monitored.

Interventions

DIETARY_SUPPLEMENTWater

Participants will receive two cups of 150ml plain water

Sponsors

Swansea University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
SINGLE (Subject)

Eligibility

Sex/Gender
ALL
Age
18 Years to 35 Years
Healthy volunteers
Yes

Inclusion criteria

* In good general health i.e. no major health condition such as diabetes * BMI \< 30

Exclusion criteria

* Not on blood pressure medication or blood thinning medication such as aspirin - No learning difficulty such as dyslexia * Diabetes * Gastro-intestinal disease * High BMI * Cholesterol and BP * Smoker * Dyslexic/dyspraxic * Depression or history of depression or other psychiatric disorder

Design outcomes

Primary

MeasureTime frameDescription
Episodic memory - list of 30 wordschange from 0 to 180 minutes after the start of the dehydration protocolParticipants listen to a list of 30 words presented using a tape recorder. The words are of similar difficulty and matched for the number of syllables and frequency with which they occur in English. The subjects are asked to recall and write down as many words as possible. The difference in the total number of words remembered from baseline (before the intervention) is analysed.
Focused attention - Eriksen Flanker Taskchange from 0 to 180 minutes after the start of the dehydration protocolThe Arrow Flankers test measures the ability to direct attention and ignore peripheral information. Participants are required to indicate whether the middle arrow is pointing to the right or left by pressing the corresponding arrow on the keyboard. Either side of the central arrow are distractors. Both the average reaction times (in milliseconds) and accuracy are recorded. The difference in performance from baseline (before the intervention) is analysed.

Secondary

MeasureTime frameDescription
Thirst (Participants rate their thirst)change from 0 to 180 minutes after the start of the dehydration protocolParticipants rate their thirst

Other

MeasureTime frameDescription
Amount of weight lost due to dehydration protocol180 minutesparticipants will be weighed at the start and end of the dehydration protocol and % weight loss calculated
Body temperature180 minutesChange in body temperature will be monitored throughout
Urine Osmolality180 minutesUrine samples will be collected at the start and end of the procedure so that changes in osmolality can be measured.

Countries

United Kingdom

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 12, 2026