Actively Recruiting

Phase Not Applicable
Age: 50Years +
All Genders
Healthy Volunteers
NCT05843318

Water Intake and Weight Control in Older Adults

Led by Virginia Polytechnic Institute and State University · Updated on 2025-11-14

375

Participants Needed

1

Research Sites

228 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

This study is a randomized controlled intervention trial in adults aged 50+ years with overweight or obesity, which will compare three groups with different diet prescriptions: 1) pre-meal water consumption (500 ml, before each main meal) with a hypocaloric diet; 2) 1500 ml water consumed throughout the day with a hypocaloric diet; 3) hypocaloric diet with no instructions regarding water consumption. Smart water bottles will objectively assess water intake timing and volume. Urine osmolality, urine volume, and serum osmolality will be used as objective indicators of compliance with the water intake prescription. We will investigate changes in perceived hunger and fullness and appetite-regulating hormones as potential mechanisms by which premeal water could improve appetite regulation. We will also investigate the impact of water consumption and hydration on executive function capabilities, which may influence intervention adherence. Although increasing water intake could be an effective weight management strategy, no evidence-based recommendations exist for the timing of water intake needed for this benefit.

CONDITIONS

Official Title

Water Intake and Weight Control in Older Adults

Who Can Participate

Age: 50Years +
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Aged 50 years or older
  • Body mass index (BMI) of 25 kg/m2 or higher
  • Weight stable within plus or minus 2 kilograms in the past 6 months
  • Willing to provide consent and follow the study protocol
Not Eligible

You will not qualify if you...

  • Usually drinks more than 1500 ml of plain water daily
  • Uncontrolled hypertension with blood pressure greater than 159/99 mmHg
  • Medical conditions needing a special diet, such as type 2 diabetes or heart failure with fluid restrictions
  • Medical conditions preventing participation in physical activity, like orthopedic injury
  • Current or past gastrointestinal diseases, surgeries, or medications affecting digestive function
  • Allergies or dislikes to foods included in the study meals

AI-Screening

AI-Powered Screening

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Trial Site Locations

Total: 1 location

1

Virginia Tech

Blacksburg, Virginia, United States, 24061

Actively Recruiting

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Research Team

B

Brenda Davy, PhD RDN

CONTACT

E

Elaina Marinik, PhD

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

TRIPLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

3

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