Actively Recruiting
Pediatric Health Empowerment: Improving Children's Perioperative Experiences with Patient-Reported Measures
Led by Gødstrup Hospital · Updated on 2026-04-23
250
Participants Needed
3
Research Sites
104 weeks
Total Duration
On this page
Sponsors
G
Gødstrup Hospital
Lead Sponsor
A
Aarhus University Hospital
Collaborating Sponsor
AI-Summary
What this Trial Is About
This research aims to improve the perioperative experiences of children aged 4 to 12 undergoing surgery and general anesthesia. It focuses on translating and validating the Pediatric Scale for Quality of Recovery (PedSQoR) into Danish and developing a new patient-reported experience measure (PREM) specifically designed for children's perspectives. The study highlights the importance of including children's own voices to reduce anxiety and improve outcomes in pediatric anesthesia and surgery. The study includes two parts: first, adapting and validating the PedSQoR through a prospective cohort study with about 150 Danish children undergoing various surgeries. Second, developing a PREM instrument using the Warwick Patient Experiences Framework, involving expert child panels, focus groups, and pilot testing with 20 children to ensure the questionnaire captures key experience dimensions. Both studies are conducted at the Department of Anesthesiology and Intensive Care at Gødstrup Hospital. Participants will complete surveys and questionnaires assessing their recovery and experiences from enrollment until four weeks after surgery. Data collection involves medical records, mailed surveys, and interviews. Researchers will analyze the reliability and validity of the tools and use thematic analysis for qualitative data. Safety and comfort of child participants are prioritized, with consent obtained from both parents and children. The total participation time ranges from enrollment through four weeks post-surgery.
CONDITIONS
Brief Title
Pediatric Anesthesia: The Childs Voice
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Pediatric patients aged 4 to 12 years
- American Society of Anesthesiologists physical status classification (ASA) I-III
- Undergoing surgery
You will not qualify if you...
- Children with cognitive or sensory disorders
- Children or parents who do not speak Danish
- Patients without consent to participate
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
Duration - Up to 4 weeks after surgery
Participants complete questionnaires to assess their recovery and experiences after surgery and anesthesia.
Questionnaires completed remotely after surgery
Trial Site Locations
Total: 3 locations
1
Aarhus University Hospital
Aarhus, Central Jutland, Denmark, 8200
Actively Recruiting
2
Copenhagen University Hospital
Copenhagen, Region Sjælland, Denmark, 2100
Actively Recruiting
3
Gødstrup Hospital
Herning, Denmark, 7400
Actively Recruiting
Research Team
J
Johanna Arnbjørn C Arnbjørn
A
Anne Højager Nielsen, Ph.D.
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
1
Similar Trials
Frequently Asked Questions
Have more questions? Get in touch with our team for quick support
Not the Right Trial for You?
Explore thousands of other clinical trials that might be a better match.
Sign up to get personalized trial recommendations delivered to your inbox.
Already have an account? Log in here