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Water Intervention for Thinking in Kids (WITiKids ) Study

The Effects of Hydration on Brain, Cognition, Memory & Achievement in Childhood

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02816450
Acronym
WITiKids
Enrollment
30
Registered
2016-06-28
Start date
2014-06-30
Completion date
2018-06-30
Last updated
2018-07-31

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

Conditions

Low Fluid Intake, Chronic

Keywords

Water, Children, Cognition, Hydration

Brief summary

The aim of this study is to determine the influence of changes in water intake on changes in cognitive function among preadolescent children. Further, the proposed work will determine the relationship between urinary markers of hydration process and cognitive function. We hypothesize that an increase in water intake will result in greater cognitive performance. In addition, improvements in hydration demonstrated by lower urine concentration will be correlated with greater cognitive performance.

Interventions

BEHAVIORALWater Intake

Sponsors

Danone Global Research & Innovation Center
CollaboratorINDUSTRY
University of Illinois at Urbana-Champaign
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
OTHER
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
9 Years to 10 Years
Healthy volunteers
Yes

Inclusion criteria

1. Parental/guardian consent 2. Normal or corrected-to-normal vision based on the minimal 20/20 standard in order to complete the cognitive task (below 20/20 vision).

Exclusion criteria

1. Participants younger than 9 years and older than 10 years at the time of testing age. 2. Prior diagnosis of cognitive or physical disability, including ADHD (severe asthma, epilepsy, chronic kidney disease, and dependence upon a wheelchair/walking aid). 3. Use of anti-psychotic, anti-depressant, anti-anxiety medication, as well as those medications used for ADD/ADHD (use of any anti-psychotic, anti-depressant, anti-anxiety, and ADD/ADHD medications). 4. Participants must have not yet reached, or be in the earliest stages, of puberty, as measured by a modified test of the Tanner Staging System 5. IQ below 85 6. Use of medications that alter urinary excretion and water metabolism 7. Use of internal electronic device, such as a pacemaker

Design outcomes

Primary

MeasureTime frame
Flanker Task Accuracy2 Hours on the morning of Day 5

Secondary

MeasureTime frame
Urine Osmolality24 hours during final day of fluid intake modulation (Day 4)

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 1, 2026