Pediatric Perioperative Satisfaction Questionnaire
For patients and families
In plain language
An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.
- What is being studied
- This is an observational study: the protocol does not assign a study treatment.
- Who it may be relevant to
- Registry conditions: Perioperative, Children, Satisfaction. Basic parameters: 7 years — 17 years · All.
- What needs checking
- Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
- Where it takes place
- France
- Next step
- Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Unsure about the terms? Read our patient guide →
Official title
Development and Validation of a Perioperative Satisfaction Questionnaire in Children Population
Overview
The aim of this study is to develop and validate a self-report questionnaire to evalutate the satisfaction of the children after surgery.
Detailed description
Step 1 : development of the questiontionnaire Face to face interview to report the satisfaction of the children after surgery and to identify recurrent themes to generate questions.
Step 2 : validation of the questionnaire Evaluation of the psychometric validity of the final questionnaire
Primary outcome measures
- Children satisfaction after surgery [Time frame: at discharge of hospital ( from the day of surgery up 14 days)]
Secondary outcome measures (2)
- postoperative pain intensity [Time frame: at discharge of hospital ( from the day of surgery up 14 days)]
- perioperative anxiety level [Time frame: at discharge of hospital ( from the day of surgery up 14 days)]
Eligibility criteria
Inclusion criteria
- children 7 years and older
- elective surgery
- general anesthesia
- abiliy to understand and read questions
Exclusion criteria
- emergency
- cognitive trouble
- intellectual disability
Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.
Healthy volunteers: Yes
Study design
- Observational model
- Cohort
Study locations
France · 6 centers
- Uhmontpellier — Montpellier
- UH Bordeaux — Bordeaux
- UH Grenoble — Grenoble
- UH Nîmes — Nîmes
- UH Reims — Reims
- UH Toulouse — Toulouse
Publications
- Bringuier S, Dadure C, Evain JN, Kern D, Michelet D, Auquier P, Aouinti S, Molinari N, Sola C, Capdevila X, Pico J; EVANpedia Study Group*. Development and Validation of EVANpedia for the Assessment of Perioperative Experience in Pediatric Patients. Anesthesiology. 2026 Jun 1;144(6):1316-1328. doi: 10.1097/ALN.0000000000006038. Epub 2026 Mar 16. PMID 41838953
Identifiers
NCT: NCT04608968 · RECHMPL20_0346