Menu
Enrolling by invitation NCT07256587

Morning Water Study

No phase Interventional Energy

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: Drink 24 ounces of water.
Who it may be relevant to
Registry conditions: Energy. Basic parameters: from 18 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 States
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →

Unsure about the terms? Read our patient guide →

Official title

Wake Up to Water: Splash Into Morning Energy!

Overview

This study aims to determine the efficacy of morning water consumption on reducing fatigue and boosting daily productivity. Participants will receive personalized feedback on how their morning hydration influences their energy levels, enabling them to make informed decisions on optimizing their daily performance for a more energized life.

Interventions

  • Other Drink 24 ounces of water
    Participants are asked to drink 24 ounces of water first thing upon waking in the morning for 30 days.

Primary outcome measures

  • PROMIS Short Form v1.0 - Fatigue 8a [Time frame: Baseline and 30 days]
  • Neuro-QOL Item Bank v1.0 -Fatigue - Short Form [Time frame: Baseline and 30 days]

Eligibility criteria

Inclusion criteria

  • all individuals over the age of consent

Exclusion criteria

  • Individuals with Hyponatremia
  • Individuals with Kidney Issues
  • Individuals with Gastrointestinal Disorders
  • Individuals in Occupations with Limited Bathroom Access
  • Individuals with Fluid Restrictions
  • Individuals Prone to Electrolyte Imbalance

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

Healthy volunteers: Yes

Study design

Allocation
N/A
Model
Single group
Masking
Open label
Primary purpose
Other

Study locations

United States · 1 center
  • Efforia — New York

Identifiers

NCT: NCT07256587 · 37282

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗