As this is only a questionnaire response, patients can have any medical conditions. Parents and medical staff are interviewed regardless of illness.
Conditions
Interventions
Group 1: The aim of this study is to investigate the preferences of children (6 - <18 years), parents (of children aged 0 - <18 years) and healthcare professionals (nurses and paediatricians) regardin
Sponsors
Klinik für Allgemeine Pädiatrie, Neonatologie und Kinderkardiologie, Universitätsklinik Düsseldorf
Eligibility
Sex/Gender
All
Age
6 Years to No maximum
Inclusion criteria
Inclusion criteria: 1. Age Children aged 6-<12y and adolescents 12-<18y, parents of children aged 0-<18 y. 2. Sex For children aged 6-<18y, 50% male and 50% female have to be included. 3. Health Parents of all children are approached independent from health status. Children aged 6-<18y must be able to read and understand the questionnaires. 4. Compliance Participants, participants’ parents, nurses, and paediatricians understand and are willing, able, and likely to comply with the survey procedures. 5. Consent Participant, participant’s parents, nurses and paediatricians are capable of understanding the survey procedures and have indicated their consent with a cross on the questionnaire. 6. Affiliation Children who participate in the study and children whose parents participate in the study must be patients at the Department of General Paediatrics, Neonatology and Paediatric Cardiology of the University Hospital Düsseldorf. Nurses and paediatricians must be employees of the Department of General Paediatrics, Neonatology and Paediatric Cardiology of the University Hospital Düsseldorf.
Exclusion criteria
Exclusion criteria: 1. Disease/Illness Children aged 6-<18y that are unable to understand and read the questionnaire on their own (e.g., due to cerebral palsy), as assessed by the Investigator. 2. Intervention 2.1. Children in the post-operative period who are not yet fully awoke 2.2. Children that are not fully oriented for whatever reason 2.3. Children 6-<18 years of age, parents, nurses, and paediatricians not willing to complete the respective questionnaire
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| To identify the best accepted oral formulation rated by children 6-<12y, and adolescents 12-<18y. To identify the best accepted oral formulation rated by parents of children 0-<2y, and 2-<6y. | — |
Secondary
| Measure | Time frame |
|---|---|
| - To identify the best accepted oral formulation rated by parents of the children 6-<12y, 12-<18y - To identify the oral formulation considered best for different age groups by nurses - To identify the oral formulation considered best for different age groups by paediatricians - To investigate the percentage of participation refusals per cohort | — |
Countries
Germany
Contacts
Public ContactViviane Klingmann
Universitätsklinik Düsseldorf, Heinrich-Heine Universität Düsseldorf, Klinik für Allgemeine Pädiatrie, Neonatologie und Kinderkardiologie
Outcome results
None listed