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Psychophysical Tracking Method to Measure Taste Preferences in Children and Adults
Published on: July 16, 2016
Children's Preferences for Oral Dosage Forms and Their Involvement in Formulation Research via EPTRI (European
Elisa Alessandrini1, Francis Brako1,2, Mariagiovanna Scarpa1
1Department of Pharmaceutics, University College London School of Pharmacy, 29-39 Brunswick Square, London WC1N 1AX, UK.
Insights
Children prefer traditional liquid, tablet, and capsule medicines, with preferences varying by age and health. Involving children in research is crucial for developing acceptable pediatric formulations.
Area of Science:
- Paediatric Pharmacology
- Formulation Science
- Patient-Centric Drug Development
Background:
- Limited data exists on children's preferred formulation characteristics, hindering tailored paediatric dosage form design.
- The European Paediatric Translational Research Infrastructure (EPTRI) initiated research to address this knowledge gap.
Purpose of the Study:
- To evaluate children's perceived preferences for oral dosage forms across several European countries.
- To explore the feasibility of involving young persons advisory groups (YPAGs) in paediatric formulation research.
Main Methods:
- An online, age-adapted survey was developed and translated into six languages.
- The survey was disseminated across seven European countries, gathering responses from 1172 participants.
- Data analysis focused on perceived preferences based on age, health status, and medication experience.
Main Results:
- Conventional dosage forms (liquid, tablets, capsules) were most preferred.
- Liquid formulations were favored by younger children (<12 years) and those rarely taking medication.
- Adolescents and children with chronic conditions preferred monolithic solid forms; novel forms like films and granules were unfamiliar and often disliked, especially by adolescents.
Conclusions:
- Children's preferences for oral dosage forms are influenced by age, health status, and medication frequency.
- Novel dosage forms require further development and acceptance assessment in paediatric populations.
- Involving children as active stakeholders and utilizing tools to assess their perspectives are essential for acceptable paediatric formulation development.
Abstract:
The paucity of evidence-based data on formulation characteristics preferred by the children is known to limit the design of tailored paediatric dosage forms. The European Paediatric Translational Research Infrastructure (EPTRI) commissioned a study to evaluate children's dosage forms perceived preferences in some European countries and explore the feasibility of using the young persons advisory groups (YPAGs) to involve children in formulation research. An online, age-adapted survey was developed and translated into six languages. The survey link was disseminated across seven European countries: Albania, Italy, the Netherlands, and Dutch-speaking part of Belgium, Romania, Spain, and the United Kingdom. Respondents' (n = 1172) perceived preferences for oral dosage forms primarily differed based on age, health status, and experience. Conventional dosage forms, i.e., liquid (35%), tablets (19%), and capsules (14%), were the most selected. Liquid was widely selected by children less than 12 years and by those healthy and taking medicines rarely. Monolithic solid forms were mostly chosen by adolescents and by children with a chronic disease taking medicines frequently. There was a clear lack of familiarity with more novel dosage forms (e.g., orodispersible films and granules). Noteworthy, granules were not appreciated, particularly by adolescents (52.8%). To rationalise the creation of paediatric formulations, it is important to involve children as active stakeholders and to apply tools assessing children's perspectives on medicines to inform acceptable dosage form development from the start.
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