Giving Children a Voice in Paediatric Anaesthesia (TR-VP26)

Patient, Parent and Clinician Voices - Establishing National and International Research Priorities for Paediatric Anaesthesia and Perioperative Medicine

This project will identify the research priorities for paediatric anaesthesia and perioperative medicine in participating countries and highlight areas where further research and information can be provided to optimise the experience of children undergoing medical interventions.

This is expected to have significant positive impacts on patient and family engagement and interest in research within the community and aids to plan patient/ family-centred studies.

Study Overview

Detailed Description

Prospective online surveys will be conducted to generate national priority research topics. Three separate series of surveys will be conducted:

  1. Children and young people aged 6 to 16 years of age
  2. Parents and caregivers
  3. Clinicians

The first round of surveys will be broad idea generating surveys. The survey will consist of a short introduction and demographic questions followed by space to input three free text suggestions for research topics. In order not to bias the suggestions, we will not provide any examples of thematic prompts, research ideas will be entirely de novo. These surveys will be open for three months.

A second round of online surveys will then be conducted to prioritise national longlist of research ideas. Respondents will be asked to pick what they consider to be the 10 most important research ideas from the longlist.

Study Type

Observational

Enrollment (Estimated)

1040

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Contact

Study Contact Backup

Study Locations

    • Canton Ticino
      • Bellinzona, Canton Ticino, Switzerland, 6500
        • Ospedale regionale Bellinzona
        • Contact:
    • Canton of Aargau
      • Aarau, Canton of Aargau, Switzerland, 5001
        • KSA
        • Contact:
    • Canton of Basel-City
      • Basel, Canton of Basel-City, Switzerland, 4001
    • Canton of Bern
      • Bern, Canton of Bern, Switzerland, 3010
    • Canton of Fribourg
      • Fribourg, Canton of Fribourg, Switzerland, 1708
    • Canton of Geneva
      • Geneva, Canton of Geneva, Switzerland, 1205
    • Canton of Lucerne
      • Lucerne, Canton of Lucerne, Switzerland, 6000

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

  • Child
  • Adult
  • Older Adult

Accepts Healthy Volunteers

Yes

Sampling Method

Non-Probability Sample

Study Population

Participating hospitals in Switzerland

Description

Inclusion Criteria:

  • Patients aged 6-16 years
  • Caregivers of patients aged 6-16 years
  • Clinicians working in paediatric perioperative medicine

Exclusion Criteria:

  • Patients <6 and >16 years
  • Residence not in Switzerland
  • Inability to understand one of the 3 study languages (german, french, italian)

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

Cohorts and Interventions

Group / Cohort
Patients
Children aged 6-16 years that require a surgical procedure
Healthcare providers
Healthcare providers working in pediatric perioperative medicine that are part of the multidisciplinary team of professionals who care for children before (preoperative), during (intraoperative), and after (postoperative) a surgical or diagnostic procedure. They can be nurses, doctors.
Parents
Parents of the children requiring a surgical procedure

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Consensus-ranked list of top 10 research priorities for paediatric anaesthesia and peri-operative medicine among children and young people aged 6-16 years, parents and clinicians.
Time Frame: 1 year
The number and rank order of research priorities identified and agreed upon by children, parents and clinicians, as determined by a prioritisation process. Priorities will be gathered via structured online surveys. The outcome is expressed as a ranked list of 10 discrete research topics, ordered by level of group consensus agreement; results are reported as the proportion (%) of participants selecting each topic as a priority, used to generate a ranked top 10 list
1 year

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Degree of agreement between child/young person-identified priorities and those identified by parents/carers and clinicians
Time Frame: 1 year
Whether child-identified priorities differ from those identified by parents/carers and clinicians and if these priorities differed from those previously identified by parents/carers and clinicians in equivalent Australian studies.
1 year

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Study Director: Thomas Riva, Prof. Dr. med., Inselspital, Bern University Hospital, Department Anesthesiology and Pain Medicine

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Estimated)

April 27, 2026

Primary Completion (Estimated)

September 30, 2027

Study Completion (Estimated)

December 31, 2027

Study Registration Dates

First Submitted

April 1, 2026

First Submitted That Met QC Criteria

April 9, 2026

First Posted (Actual)

April 13, 2026

Study Record Updates

Last Update Posted (Actual)

April 13, 2026

Last Update Submitted That Met QC Criteria

April 9, 2026

Last Verified

April 1, 2026

More Information

Terms related to this study

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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