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Clinical Trial Summary

This is a double-blind, controlled, parallel, randomized sensory study. The study will consist of two cohorts; habitual regular full-calorie Carbonated Soft Drink (CSD) consumers and habitual low-calorie CSD consumers. Each cohort will be randomized to one of 3 interventions for six months (24 weeks):

- Intervention 1: Control (full sweetness) beverage

- Intervention 2: Step-wise sweetness reduction series of beverages

- Intervention 3: Moderate sweetness (reduced sweetness) beverage

The primary outcome is to assess the perception changes in sweetness (magnitude scale) and sweetness liking (Likert scale) of a test product and a control product over a period of six months. The study endeavors to explore whether consumers of sweetened carbonated beverages can adapt liking to lower sweetness beverages after prolonged exposure of daily consumption of beverages with step-wise reduction of sweetness, or maintenance at reduced (moderate) sweetness.

The secondary outcome will be to assess dietary compensation for sweetness in the step-wise and moderate reduction arms compared to the control arms (the full calorie and low calorie control beverages). Dietary analysis of calories and intakes of total sugar, added sugar, and servings of low-/non-calorie sweeteners will be assessed using a 3-day diet record pre-intervention and monthly for 6 months.


Clinical Trial Description

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Study Design


Related Conditions & MeSH terms


NCT number NCT04284462
Study type Interventional
Source PepsiCo Global R&D
Contact
Status Terminated
Phase N/A
Start date January 14, 2020
Completion date March 11, 2020

See also
  Status Clinical Trial Phase
Completed NCT04609657 - Liking Adaptation to Beverages With Varying Sweetness Levels After Prolonged Exposure N/A
Completed NCT05010408 - Liking Adaptation to Beverages of Varying Sweetness Levels Following Prolonged Exposure N/A