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SipSmarter: A Nutrition Literacy Approach to Reducing Sugary Beverages

SipSmarter: A Nutrition Literacy Approach to Reducing Sugary Beverages

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02193009
Enrollment
304
Registered
2014-07-17
Start date
2011-07-31
Completion date
2015-12-31
Last updated
2022-04-27

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Dietary Habits, Physical Activity

Brief summary

The primary aim of this pragmatic randomized-controlled trial was to determine the effectiveness of a scalable 6-month intervention aimed at decreasing SSB consumption (SIPsmartER) when compared to a matched contact physical activity promotion control group (MoveMore).

Detailed description

The primary aim of this application targeting at-risk residents from rural southwest Virginia counties is to: 1\. Determine the effectiveness of SIPsmart and SIPsmartER at decreasing SSB consumption when compared to a matched contact control group targeting walking behaviors. The secondary aims are to: 1. Explore causal pathways through which changes in SSB attitudes, subjective norms, and perceived behavioral control influence behavioral intentions and SSB consumption, and the extent to which changes in SSB consumption are mediated by changes in nutrition numeracy and nutrition-related media literacy. 2. Determine the reach and representativeness, adoption feasibility, degree to which the intervention was implemented as intended (and associated costs), and the maintenance of behavior changes 6 and 12 months post intervention (i.e., 18 months from baseline) when compared to control. 3. Assess intervention impacts on body weight. An exploratory aim is to: 1\. Assess intervention impacts on a 13C biomarker, a new non-invasive biomarker fingerstick technique for added sugar intake, and evaluate the changes in this biomarker over time.

Interventions

BEHAVIORALSipSmarter

6-month behavioral trial

BEHAVIORALMoveMore

6 month behavioral trial

Sponsors

University of Kansas
CollaboratorOTHER
University of Hawaii
CollaboratorOTHER
Virginia Polytechnic Institute and State University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

* Inclusion criteria included English-speaking adults \>18 years of age, who consume \>200 SSB kcals/day, self-report no contraindications for physical activity, and have regular access to a telephone.

Exclusion criteria

* To minimize potential confounds, only one member per household is eligible to enroll and individuals cannot be concurrently enrolled in a Cooperative Extension program because these programs focus on improving nutrition.

Design outcomes

Primary

MeasureTime frame
Change from Baseline in Kilocalories of Sugar-Sweetened Beverages at 6 monthsbaseline, 6-months

Secondary

MeasureTime frame
Change from Baseline in Minutes of Physical Activity at 6 monthsbaseline, 6-months

Other

MeasureTime frame
Change from Baseline in Weight at 6 monthsbaseline, 6-months
Change from Baseline in C13 biomarker at 6 monthsbaseline, 6-months

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 17, 2026