Actively Recruiting
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
Eligibility Criteria
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
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
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Trial Site Locations
Total: 1 location
1
Virginia Tech
Blacksburg, Virginia, United States, 24061
Actively Recruiting
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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