Hydration
Conditions
Keywords
Infants, Water, Safety
Brief summary
The present study evaluates the safety of ROSA oligomineral water in 6-to-12-month old healthy children.
Detailed description
Our study is designed as an open-label case-control interventional study that evaluates the safety of 28-day hydration with ROSA water in healthy infants aged 6-12 months. The participants are apparently healthy children breastfed or formula fed; minimal sample size (n = 52) was calculated according to 0.8 power to detect a significant difference in the prevalence of diarrhea (G\*Power 3.1). Final group of participants will consist of sixty-five healthy male and female infants (we presume that 20% of participants will drop-out throughout the study). The stopping rules for participants include a refuse to participate in this research at any time and significant change of health status. All participants will be allocated in an open-label manner to two randomly assigned ad libitum hydration regimens: first group will receive ROSA water for daily hydration, and second (control) group will receive other water of personal choice (including tap water). All testing including parental diary of infant general status (e.g. daily amount of water consumed, number of stools per day, nutritional habits) and clinician-reported outcomes (e.g. body weight, clinical evaluation of hydration will be conducted at pre-administration (baseline) and at follow-up (after 28 days of administration). The study is entirely voluntary and the participants are free to stop participating at any time.
Interventions
Ad libitum hydration with ROSA oligomineral water
Ad libitum hydration with other waters
Sponsors
Study design
Intervention model description
All participants will be allocated in an open-label manner to two randomly assigned ad libitum hydration regimens: first group will receive ROSA water for daily hydration, and second (control) group will receive other water of personal choice (including tap water)
Eligibility
Inclusion criteria
* Age 6 to 12 months * Healthy children * Doubled weight at 6 months * Tripled weight at 12 months * Feed with breast milk of milk formula
Exclusion criteria
* Any acute or chronic disease * Unwillingness to return for follow-up analysis
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Daily amount of water consumed | Baseline vs. 28-days | Monitor change in daily amount of water consumed |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Number of stools per day | Baseline vs. 28-days | Monitor change in number of stools per day |
| Body weight | Baseline vs. 28-days | Monitor change in body weight |
| Hydration status | Baseline vs. 28-days | Monitor clinican-reported change in hydration status |
Countries
Serbia