N/A
N=1,013
Kids SipSmartER, an Intervention to Reduce Sugar-sweetened Beverages
Sugary Beverages
Bottom Line
View on ClinicalTrials.gov: NCT03740113 ↗Enrolled (actual)
1,013
Serious AEs
0.0%
Results posted
Apr 2025
Primary outcome: Primary: Student: SSB Change From Baseline to 7-months (All Participants) — -9.9; -2.7 fluid ounces
Study Design & Population
- Study type
- Interventional
- Phase
- N/A
- Interventions
- Kids SipSmartER (Behavioral)
- Age
- Pediatric, Adult, Older Adult · 10+ yrs
- Sex
- All
- Sponsor
- University of Virginia
- Primary completion
- May 2022
Outcome Measures
| Outcome | Result | p-value |
|---|---|---|
| PRIMARY Student: SSB Change From Baseline to 7-months (All Participants) |
-9.9; -2.7 | — |
| SECONDARY Caregiver: SSB Change From Baseline to 7-months (All Participants) |
-8.2; -6.3 | — |
| SECONDARY Student: BMI Z-score Change From Baseline to 7-months |
0.02; -0.018 | — |
| SECONDARY Caregiver: BMI Change From Baseline to 7-Months |
-0.3; -0.65 | — |
| SECONDARY Student and Caregiver: Quality of Life Change From Baseline to 7-months--Overall Health Rating |
0.06; 0.03; 0.04; -0.06 | — |
| SECONDARY Caregiver: Quality of Life Change From Baseline to 7-months--Unhealthy Days |
-0.3; -1.7 | — |
| SECONDARY Student: Quality of Life Change From Baseline to 7-months--school Related Function |
-1.7; -3.9 | — |
Summary
Overall Goal: To determine the effectiveness of Kids SIPsmartER in improving sugar-sweetened beverages behaviors among 7th grade students. Secondary aims are to determine (1) changes in secondary student outcomes (e.g. quality of life, BMI z-score, theory-related variables, health and media literacy), (2) changes in caregiver SSB behaviors and home environment, (3) maintenance of outcomes at 19-months post-baseline, (4) assess the reach and representativeness of Kids SIPsmartER, among students and caregivers, and (5) implementation, adoption, and maintenance among teachers and schools.
Eligibility Criteria
Inclusion Criteria
- 7th grade students in the 12 enrolled schools during the years their school is randomized to one of these cohorts are eligible to participate
- Parents/caregivers of enrolled middle school students
Exclusion Criteria
- Data from students with major cognitive disabilities that could compromise self-report behavioral data quality will be excluded
Data sourced from ClinicalTrials.gov (NCT03740113). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.