Development and Validation of EVANpedia for the Assessment of Perioperative Experience in Pediatric Patients.
Sophie Bringuier, Christophe Dadure, Jean-Noël Evain...
https://pubmed.ncbi.nlm.nih.gov/41838953Actively Recruiting
Age: 7Years - 17Years
All Genders
Healthy Volunteers
ID04608968
Development and Validation of a Perioperative Satisfaction Questionnaire in Children Population
Led by University Hospital, Montpellier · Updated on 2024-11-27
600
Participants Needed
6
Research Sites
N/A
Total Duration
On this page
AI-Summary
What this Trial Is About
This research aims to develop and validate a questionnaire to measure how satisfied children are after surgery. It focuses on pediatric patients aged 7 to 17 years who have undergone elective surgery with general anesthesia. The goal is to create a reliable tool that captures children's feelings about their surgical experience and recovery. The study is conducted in two main steps. First, researchers interview children face-to-face to understand their satisfaction and identify common themes, which helps generate questionnaire items. Second, they evaluate the final questionnaire's psychometric validity to ensure it accurately reflects children's satisfaction levels. Participants will be assessed around the time of hospital discharge, from the day of surgery up to 14 days afterward. Researchers will measure children's satisfaction, postoperative pain intensity, and anxiety levels during this period. The study includes questionnaires and interviews, with data collected to validate the new satisfaction tool.
CONDITIONS
Brief Title
Pediatric Perioperative Satisfaction Questionnaire
Who Can Participate
Age: 7Years - 17Years
All Genders
Healthy Volunteers
Eligibility Criteria
You may qualify if you...
- Children aged 7 years and older
- Undergoing elective surgery
- Receiving general anesthesia
- Able to understand and read questions
You will not qualify if you...
- Emergency surgery
- Cognitive trouble
- Intellectual disability
AI-Screening
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Your Study Journey
Screening
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
Surgery and Immediate Post-operative Care
Duration - From the day of surgery up to 14 days
Participants undergo elective surgery with general anesthesia and are observed immediately after surgery.
1 perioperative visit and assessments until hospital discharge
Post-operative Follow-up
Duration - Up to 14 days after surgery
Participants complete questionnaires to report satisfaction, pain intensity, and anxiety levels after surgery to validate the questionnaire.
1 to 2 follow-up visits depending on recovery and questionnaire completion
Trial Site Locations
Total: 6 locations
1
Uhmontpellier
Montpellier, Montpellier, France, 34295
Actively Recruiting
2
UH Bordeaux
Bordeaux, France
Actively Recruiting
3
UH Grenoble
Grenoble, France
Actively Recruiting
4
UH Nîmes
Nîmes, France
Actively Recruiting
5
UH Reims
Reims, France
Actively Recruiting
6
UH Toulouse
Toulouse, France
Actively Recruiting
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Research Team
S
sophie Bringuier
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
0
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