Pediatric AnesthesiaPHEASENCT07289152
Pediatric Anesthesia: The Childs Voice
An observational study of Pediatric Anesthesia and Pediatric Surgery, run by Gødstrup Hospital at 3 sites in Denmark.
Trial summary
In Denmark, around 25,000 children under 18 undergo general anesthesia annually. Hospital stays and anesthesia can induce significant anxiety and stress in children due to unfamiliar environments, procedures, and communication issues. Read more about this study
- Who is it for?
- Ages 4 to 12 years
- Conditions the study is for
- Pediatric Anesthesia, Pediatric Surgery, PROMs
- How many people
- 250 participants
- Where
- 3 sitesDenmark
- Study dates
- 1 Jan 2026to 31 Dec 2030
- Phase
- Observational
- Are there results?
- Not yet: the study is under way
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 4 to 12 years
- All sexes
- No healthy volunteers
- Child
Study population: Children undergoing surgery and general anesthesia aged 4-12 years.
Who may be able to join
- Pediatric patients aged 4-12, American Society of
- Anesthesiologists physical status classification (ASA) I-III
- undergoing surgery
Who cannot join
- Children with cognitive or sensory disorders
- children or parents who do not speak Danish,
- patients for whom there is no consent to participate.
Trial locations and contacts
3 sites in 1 country. Contact the study team or a site near you to ask about taking part.
Anne Højager Nielsen, Ph.D. contact
Denmark3 sites, 3 recruiting
- Recruiting
Aarhus University Hospital
Aarhus, Central Jutland, 8200
Louise Bill MD, PhD
- Recruiting
Copenhagen University Hospital
Copenhagen, Region Sjælland, 2100
- Recruiting
Gødstrup Hospital
Herning, 7400
Johanna C Arnbjørn, +4527141475, johkoc@onerm.dk
About this study
Official title: Pediatric Health Empowerment: Improving Children´s Perioperative Experiences With Patient-Reported Measures
In Denmark, around 25,000 children under 18 undergo general anesthesia annually. Hospital stays and anesthesia can induce significant anxiety and stress in children due to unfamiliar environments, procedures, and communication issues. This anxiety can be linked to postoperative complications such as emergence delirium and may negatively impact both the child and their family's well-being. Engaging patients actively in their healthcare, including pediatric cases, is essential for improving outcomes. Assessing perioperative patient and family outcomes, particularly through patient-reported outcome measures (PROM) and patient-reported experience measures (PREM), can significantly enhance the quality of care provided to children. While PROMs are widely used in adults, they are less common in pediatric settings. The Pediatric Scale for Quality of Recovery (PedSQoR), developed by Australian and American researchers, is one such tool designed to measure recovery in children. This study aims to translate andvalidate the PedSQoR for Danish children aged 4-12. Furthermore, no existing instruments comprehensively assess pediatric surgery patients' experiences under general anesthesia, particularly from the child's perspective without relying on parents as proxies. Empowering children to express their healthcare experiences gives healthcare workers an insight into what matters for children and gives children a more positive outlook on healthcare, benefiting lifelong engagement.
Study Aims and Objectives: The study aims to enhance the assessment of children's outcomes and experiences in perioperative settings, ultimately improving pediatric perioperative healthcare. The objectives include:
Read more
- Translation and Adaptation: a. Translate and adapt the PedSQoR for Danish children aged 4-12. b. Validate the Danish PedSQoR version.
- Development of a PREM Instrument: a. Develop a comprehensive PREM for children's experiences during surgery and anesthesia. b. Pilot-test and adjust the PREM questionnaire with a group of children aged 4-12.
Study Methods:
- PedSQoR Translation and Validation: A single-center prospective cohort study will adapt and test the PedSQoR for Danish children. The process involves translating the 21-item scale, validating it with a sample size of 150, and ensuring reliability through various statistical methods, including Cronbach's Alpha and test-retest reliability. Data will be collected from the Department of Anesthesiology and Intensive Care at Gødstrup Hospital.
- PREM Instrument Development:
This study will develop a PREM instrument using the Warwick Patient Experiences Framework (WaPEF), which encompasses seven dimensions of patient experience. The process will involve forming a panel of child experts, conducting focus groups, and translating insights into a pictorial questionnaire. The PREM will undergo pilot testing with 20 children to validate its effectiveness in capturing the dimensions of the WaPEF.
Research Ethics: Given the vulnerability of children in research, this study will prioritize their safety and comfort, ensuring the study's benefits outweigh any potential risks. Informed consent will be obtained from both parents and children. The study will be registered with the Region Central Denmark's list of research projects and will not require approval from the Scientific Ethics Committee.
Read the detailed description
Project title: Pediatric Healthcare Empowerment: Improving Children's Perioperative Experiences with Patient-Reported Measures Acronym: PHEASE
Impact:
Understanding and improving children's experiences is integral to enhancing pediatric healthcare services. Annually, approximately 6 million children worldwide undergo general anesthesia, and the potential impact on their well-being and behavior is significant. The hospital environment, inadequate communication with staff and negative postoperative experiences can contribute to anxiety and sadness, particularly due to a lack of insight into children's unique needs. The common practice of relaying information to parents or caretakers often results in the child's perspective being overlooked. This study promises to empower 4-12-year-olds to express their thoughts to enhance the perioperative experience. This study will translate a newly developed tool for measuring patient-reported outcome measures in Pediatric Scale for Quality of Recovery (PedSQoR) and create a tool for children to express their experiences so that hospital staff can improve the quality of care. The impact extends beyond immediate outcomes, with the potential for lifelong benefits for children shaping their healthcare experiences. Background In Denmark, 25,000 children under the age of 18 undergo general anesthesia annually (1).
Admission to hospitals and general anaesthesia affect children; a hospital stay can cause a child to experience anxiety about procedures, unknown environments, pain and fasting (2).
Poor communication with staff may negatively influence the mood and behavior of the child (3). Furthermore, postoperative anxiety and melancholy may be linked to the onset of emergence delirium, the disconcerting hospital setting, and a limited understanding of the unique requirements of children (4). Post-operative symptoms can impose a burden on both children and their parents, potentially requiring them to take sick leave for varying durations. However actively engaging patients in their healthcare experience improves health outcomes, a principle applicable to pediatric cases as well (5). Consequently, assessing perioperative patient and family outcomes, postoperative well-being, and experiences may improve outcomes for children undergoing anesthesia. Ferreira et al. (2023) advocate for the combined use of patient-reported outcome measures (PROM) and patient-reported experience measures (PREM). This integrated approach incorporates both the objective and subjective aspects of the patient's experience. By 2 utilizing both measures in tandem, healthcare providers can gain a more nuanced and comprehensive insight into the overall quality of care from the patient's perspective (6).
PROMs are used widely in the adult population. Patient outcomes after surgery and anaesthesia can be assessed with the 15-item Quality of Recovery Score (QoR-15) (5). For children, a group of Australian researchers have developed a 21 item Pediatric Scale for Quality of Recovery (PedSQoR) measuring children´s recovery, this will be translated and validated into Danish (7). PREMs are tools that capture patients' perspectives on their interactions with healthcare services, including their experiences with the hospital environment and staff. Heath et al.
(2023) illustrate that children's experiences during a hospital stay can differ significantly from those of their parents. Therefore, children must have a direct and independent voice in the assessment of their care (2). Following the United Nations Convention on the Rights of the Child, every child is entitled to express their views on any matters affecting them. Ensuring their right to share insights regarding their experiences, particularly in the context of a hospital visit, it is crucial to enable children to provide input on their healthcare encounters, utilizing tools such as PROM and PREM (8). No instruments have been developed to validly assess patient experiences for pediatric surgery patients undergoing general anesthesia in children, and very few instruments exist to measure children's experiences without using parents as a proxy (3, 4, 6). Previous research has shown that empowering 4-12-year-olds to express their thoughts on enhancing and making the Operating Room less daunting for them has lifelong benefits (9). When children have a say in their healthcare experiences, they tend to develop a more positive outlook, leading to reduced fear and anxiety during medical visits, ultimately contributing to improved lifelong healthcare engagement (2, 10, 11). Aim The overall aim of this study is to enable the assessment of children's outcomes and experiences in the perioperative setting, ultimately contributing to improving all pediatric healthcare. Objectives
- a. To translate and adapt the PedSQoR for Danish children aged 4-12.
- b. To validate the Danish version of the PedSQoR in children aged 4-12.
- a. To develop a comprehensive PREM for children's experiences during surgery and general anaesthesia.
- b. To pilot-test and adjust the questionnaire on a group of children aged 4-12 who have undergone surgery and anaesthesia. 3 Methods Study 1 - Translating and adaptation of the PedSQoR for Danish children Study design: Adaption and clinimetric testing in a single-centered prospective cohort study.
Construction: Translated the PedSQoR for children into Danish, the 21 items will be validated. The rating scale will use a Likert scale and tested on 10 Danish children, to confirm the ranking (7). Inclusion criteria: Pediatric patients aged 4-12, American Society of Anesthesiologists physical status classification (ASA) I-III undergoing surgery in Gødstrup Hospital (12). Exclusion criteria: Children with cognitive or sensory disorders, children or parents who do not speak Danish, and patients for whom there is no consent to participate.
Setting: Department of Anesthesiology and Intensive Care at Gødstrup Hospital where we provide anaesthesia for 1050 children annually for a variety of surgical procedures within orthopaedics, urology, and general surgery. Data collection: Baseline data will be collected from the electronic medical journal and entered into Research Electronic Data Capture (REDCap) hosted at Aarhus University. The PedSQoR survey will be distributed by mail and entered into REDCap. Statistical method: Based on previous studies a sample size of 150 participants is needed to obtain reliable power (participation proportion 50%). Clinimetric validity will be tested by convergent, construct, and discriminant validity. Reliability will be tested with internal consistency based on Cronbach´s Alpha, and test and retest reliability will be analyzed.
Responsiveness will be assessed with the Cohen size effect and standardized response mean.
The completion rate will evaluate acceptability and feasibility and the mean times to complete the PedSQoR Danish. For analyzing data, we will use STATA version 17.0 BE.
Study 2. Development of a PREM instrument for children Study design: Development of a comprehensive measuring instrument for children's experiences during surgery and general anesthesia by using the Warwick Patient Experiences Framework (WaPEF) 7 dimensions, which includes Patients as active participants, Responsiveness of services, an Individualized approach, Lived experience, Continuity of care and relationships, Communication, Information, and Support. Development of items: The process will be guided by a panel of children recruited by the local Department of Pediatrics among their chronic patients. The panel will be considered experts having considerable experience with hospitals. We will conduct four focus group sessions involving a sample of 4-5 children of the same age who have undergone general anesthesia, and supplement data with individual interviews with children as needed. The interview guide will be developed to engage children in the conversation (13). All interviews will be recorded and transcribed. 4 Questionnaire Design: Based on insights from the interviews important themes and phrases will be translated into questions and answers on a pictorial questionnaire, incorporating the identified dimensions. Pilot testing and validation: Face validity of the questionnaire will be tested on 2-3 children through either in-person or telephone interviews and adjustments will be made if deemed necessary. After the adjustments, the questionnaire will be pilot tested on a group of 20 children, to validate if the questionnaire captures the children´s experiences according to the 7 dimensions of the WaPEF. The questionnaire will be administered on paper and data will be entered into REDCap. Inclusion criteria/ exclusion criteria/ setting: same as study 1. Data analysis: Transcripts from focus group interviews will be analysed using thematic analysis aligned with the 7 generic dimensions of WaPEF (14). Through collaborative efforts, the team will formulate consistent codes, subsequently applying them to the remaining two focus group transcripts using deductive coding. A comprehensive discussion within the research team will ascertain if the seven dimensions adequately encompass all emerging themes, resolving any discrepancies. Iterative modifications to the coding process will be made to ensure thorough coverage and prevent the oversight of any dimensions.
Expected papers
- Translation and adaption of the PedSQoR for Danish children aged 4-12
- Childrens experiences of surgery and anaesthesia. A focus group study
- Development of a Pediatric Patient-Reported Experience Measurement Instrument for children aged 4-12 undergoing anesthesia and surgery Research ethics Given their vulnerability in research, children necessitate careful consideration to ensure the study neither harms nor burdens them, weighing this against the study's significance in empowering children's voices. Therefore, specialized communication strategies will be employed in interactions with children. All interviews will be carried out by the PhD student who is a highly experienced nurse anesthetist with long experience in communication with children. Informed written consent will be sought from both parents and children. The study does not mandate approval from the Scientific Ethics Committee but will be registered on the Region Central Denmark's list of research projects.
5
Organization of the project The project will be conducted at Gødstrup Hospital, with Anne Højager Nielsen Ph.D., MCN, Associate Professor serving as the main supervisor.
Co-supervisors: Veronica Pisinger Ph.D. and researcher at the National Institute of Public Health; Denmark has special insight into the validation of questionnaires. Associate Professor and nurse anesthetist Pether Jildenståhl from Lunds University, Sweden has special insight into anaesthesia and children's needs and rights.
Collaborators: A/Prof Paul Lee-Archer, BMedSci, MBBS, FANZCA, MMed(ClinEpi), PhD, Senior Staff Specialist, Anaesthesia, Queensland Children's Hospital, Associate Professor, Faculty of Medicine, University of Queensland, and Professor Andrew Davidson FAHMS, Medical Director, Melbourne Childrens Trail Centre, Murdoch Children Research Institute,will host the international research stay.
Pediatric anesthetists and staff at Gødstrup Hospital. The PhD student: Draft of the protocol, data collection, data management, and data analysis.
The manuscripts will be drafted by the Ph.D. student, who will be the primary author of all publications. The PhD student will present research findings at conferences and international events. The PhD student will disseminate Relevant results to patient organizations and the public.
- Conditions
- Pediatric Anesthesia, Pediatric Surgery, PROMs, PREMs
- Keywords
- PROM, Patient-reported outcom measues, Children, child, PREM, Patient-reported experience measures
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
| Study group | Role | What they receive |
|---|---|---|
| Children age 4-12, undergoing surgery and general anesthesia | Not described |
What is being measured
The primary outcome is the main question the study is designed to answer.
To validate the Danish version of the PedSQoR in children aged 4-12.
Measured: From enrollment to the end of week 4 after surgery
To pilot-test and adjust the questionnaire on a group of children aged 4-12 who have undergone surgery and anaesthesia
Patient Reported Experience Measure (PREM)
Measured: From enrollment to 4 weeks after surgery
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted17 Dec 2025
- Study start1 Jan 2026
- Primary completion31 Dec 2028 (estimated)
- Study completion31 Dec 2030 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Pediatric AnesthesiaStudies of the same condition, open and under way.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Observational
- Observational model
- Cohort
- Time perspective
- Prospective
- Enrolment
- 250 participants (estimated)
Sponsor and investigators
- Lead sponsor
- Gødstrup Hospital
- Sponsor type
- University, hospital or other
- Collaborators
- Aarhus University Hospital
- Responsible party
- Sponsor
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT07289152
- Sponsor's protocol ID
- 1-16-02-129-25
- Acronym
- PHEASE
- Status last verified
- Sep 2026
- First submitted
- 3 Dec 2025
- Last updated
- 10 Sep 2026
- Results posted
- No
- Data monitoring committee
- Yes
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- Undecided
Study at a glance
From the registry record, last updated by the sponsor on 10 Sep 2026. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Pediatric Health Empowerment: Improving Children´s Perioperative Experiences With Patient-Reported Measures
- ClinicalTrials.gov ID
- NCT07289152
- Acronym / sponsor ID
- PHEASE / 1-16-02-129-25
- Conditions
- Pediatric Anesthesia, Pediatric Surgery, PROMs, PREMs
- Keywords
- PROM, Patient-reported outcom measues, Children, child, PREM, Patient-reported experience measures
- Study type
- Observational
- Recruitment status
- Recruiting
- Enrolment
- 250 participants (estimated)
- Lead sponsor
- Gødstrup HospitalUniversity, hospital or other
- Collaborators
- Aarhus University Hospital
- Study start
- 1 Jan 2026 (actual)
- Primary completion
- 31 Dec 2028 (estimated)
- Study completion
- 31 Dec 2030 (estimated)
- First posted
- 17 Dec 2025 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
In Denmark, around 25,000 children under 18 undergo general anesthesia annually. Hospital stays and anesthesia can induce significant anxiety and stress in children due to unfamiliar environments, procedures, and communication issues. This anxiety can be linked to postoperative complications such as emergence delirium and may negatively impact both the child and their family's well-being. Engaging patients actively in their healthcare, including pediatric cases, is essential for improving outcomes. Assessing perioperative patient and family outcomes, particularly through patient-reported outcome measures (PROM) and patient-reported experience measures (PREM), can significantly enhance the quality of care provided to children. While PROMs are widely used in adults, they are less common in pediatric settings. The Pediatric Scale for Quality of Recovery (PedSQoR), developed by Australian and American researchers, is one such tool designed to measure recovery in children. This study aims to translate andvalidate the PedSQoR for Danish children aged 4-12. Furthermore, no existing instruments comprehensively assess pediatric surgery patients' experiences under general anesthesia, particularly from the child's perspective without relying on parents as proxies. Empowering children to express their healthcare experiences gives healthcare workers an insight into what matters for children and gives children a more positive outlook on healthcare, benefiting lifelong engagement.
Study Aims and Objectives: The study aims to enhance the assessment of children's outcomes and experiences in perioperative settings, ultimately improving pediatric perioperative healthcare. The objectives include:
- Translation and Adaptation: a. Translate and adapt the PedSQoR for Danish children aged 4-12. b. Validate the Danish PedSQoR version.
- Development of a PREM Instrument: a. Develop a comprehensive PREM for children's experiences during surgery and anesthesia. b. Pilot-test and adjust the PREM questionnaire with a group of children aged 4-12.
Study Methods:
- PedSQoR Translation and Validation: A single-center prospective cohort study will adapt and test the PedSQoR for Danish children. The process involves translating the 21-item scale, validating it with a sample size of 150, and ensuring reliability through various statistical methods, including Cronbach's Alpha and test-retest reliability. Data will be collected from the Department of Anesthesiology and Intensive Care at Gødstrup Hospital.
- PREM Instrument Development:
This study will develop a PREM instrument using the Warwick Patient Experiences Framework (WaPEF), which encompasses seven dimensions of patient experience. The process will involve forming a panel of child experts, conducting focus groups, and translating insights into a pictorial questionnaire. The PREM will undergo pilot testing with 20 children to validate its effectiveness in capturing the dimensions of the WaPEF.
Research Ethics: Given the vulnerability of children in research, this study will prioritize their safety and comfort, ensuring the study's benefits outweigh any potential risks. Informed consent will be obtained from both parents and children. The study will be registered with the Region Central Denmark's list of research projects and will not require approval from the Scientific Ethics Committee.
Detailed description
Project title: Pediatric Healthcare Empowerment: Improving Children's Perioperative Experiences with Patient-Reported Measures Acronym: PHEASE
Impact:
Understanding and improving children's experiences is integral to enhancing pediatric healthcare services. Annually, approximately 6 million children worldwide undergo general anesthesia, and the potential impact on their well-being and behavior is significant. The hospital environment, inadequate communication with staff and negative postoperative experiences can contribute to anxiety and sadness, particularly due to a lack of insight into children's unique needs. The common practice of relaying information to parents or caretakers often results in the child's perspective being overlooked. This study promises to empower 4-12-year-olds to express their thoughts to enhance the perioperative experience. This study will translate a newly developed tool for measuring patient-reported outcome measures in Pediatric Scale for Quality of Recovery (PedSQoR) and create a tool for children to express their experiences so that hospital staff can improve the quality of care. The impact extends beyond immediate outcomes, with the potential for lifelong benefits for children shaping their healthcare experiences. Background In Denmark, 25,000 children under the age of 18 undergo general anesthesia annually (1).
Admission to hospitals and general anaesthesia affect children; a hospital stay can cause a child to experience anxiety about procedures, unknown environments, pain and fasting (2).
Poor communication with staff may negatively influence the mood and behavior of the child (3). Furthermore, postoperative anxiety and melancholy may be linked to the onset of emergence delirium, the disconcerting hospital setting, and a limited understanding of the unique requirements of children (4). Post-operative symptoms can impose a burden on both children and their parents, potentially requiring them to take sick leave for varying durations. However actively engaging patients in their healthcare experience improves health outcomes, a principle applicable to pediatric cases as well (5). Consequently, assessing perioperative patient and family outcomes, postoperative well-being, and experiences may improve outcomes for children undergoing anesthesia. Ferreira et al. (2023) advocate for the combined use of patient-reported outcome measures (PROM) and patient-reported experience measures (PREM). This integrated approach incorporates both the objective and subjective aspects of the patient's experience. By 2 utilizing both measures in tandem, healthcare providers can gain a more nuanced and comprehensive insight into the overall quality of care from the patient's perspective (6).
PROMs are used widely in the adult population. Patient outcomes after surgery and anaesthesia can be assessed with the 15-item Quality of Recovery Score (QoR-15) (5). For children, a group of Australian researchers have developed a 21 item Pediatric Scale for Quality of Recovery (PedSQoR) measuring children´s recovery, this will be translated and validated into Danish (7). PREMs are tools that capture patients' perspectives on their interactions with healthcare services, including their experiences with the hospital environment and staff. Heath et al.
(2023) illustrate that children's experiences during a hospital stay can differ significantly from those of their parents. Therefore, children must have a direct and independent voice in the assessment of their care (2). Following the United Nations Convention on the Rights of the Child, every child is entitled to express their views on any matters affecting them. Ensuring their right to share insights regarding their experiences, particularly in the context of a hospital visit, it is crucial to enable children to provide input on their healthcare encounters, utilizing tools such as PROM and PREM (8). No instruments have been developed to validly assess patient experiences for pediatric surgery patients undergoing general anesthesia in children, and very few instruments exist to measure children's experiences without using parents as a proxy (3, 4, 6). Previous research has shown that empowering 4-12-year-olds to express their thoughts on enhancing and making the Operating Room less daunting for them has lifelong benefits (9). When children have a say in their healthcare experiences, they tend to develop a more positive outlook, leading to reduced fear and anxiety during medical visits, ultimately contributing to improved lifelong healthcare engagement (2, 10, 11). Aim The overall aim of this study is to enable the assessment of children's outcomes and experiences in the perioperative setting, ultimately contributing to improving all pediatric healthcare. Objectives
- a. To translate and adapt the PedSQoR for Danish children aged 4-12.
- b. To validate the Danish version of the PedSQoR in children aged 4-12.
- a. To develop a comprehensive PREM for children's experiences during surgery and general anaesthesia.
- b. To pilot-test and adjust the questionnaire on a group of children aged 4-12 who have undergone surgery and anaesthesia. 3 Methods Study 1 - Translating and adaptation of the PedSQoR for Danish children Study design: Adaption and clinimetric testing in a single-centered prospective cohort study.
Construction: Translated the PedSQoR for children into Danish, the 21 items will be validated. The rating scale will use a Likert scale and tested on 10 Danish children, to confirm the ranking (7). Inclusion criteria: Pediatric patients aged 4-12, American Society of Anesthesiologists physical status classification (ASA) I-III undergoing surgery in Gødstrup Hospital (12). Exclusion criteria: Children with cognitive or sensory disorders, children or parents who do not speak Danish, and patients for whom there is no consent to participate.
Setting: Department of Anesthesiology and Intensive Care at Gødstrup Hospital where we provide anaesthesia for 1050 children annually for a variety of surgical procedures within orthopaedics, urology, and general surgery. Data collection: Baseline data will be collected from the electronic medical journal and entered into Research Electronic Data Capture (REDCap) hosted at Aarhus University. The PedSQoR survey will be distributed by mail and entered into REDCap. Statistical method: Based on previous studies a sample size of 150 participants is needed to obtain reliable power (participation proportion 50%). Clinimetric validity will be tested by convergent, construct, and discriminant validity. Reliability will be tested with internal consistency based on Cronbach´s Alpha, and test and retest reliability will be analyzed.
Responsiveness will be assessed with the Cohen size effect and standardized response mean.
The completion rate will evaluate acceptability and feasibility and the mean times to complete the PedSQoR Danish. For analyzing data, we will use STATA version 17.0 BE.
Study 2. Development of a PREM instrument for children Study design: Development of a comprehensive measuring instrument for children's experiences during surgery and general anesthesia by using the Warwick Patient Experiences Framework (WaPEF) 7 dimensions, which includes Patients as active participants, Responsiveness of services, an Individualized approach, Lived experience, Continuity of care and relationships, Communication, Information, and Support. Development of items: The process will be guided by a panel of children recruited by the local Department of Pediatrics among their chronic patients. The panel will be considered experts having considerable experience with hospitals. We will conduct four focus group sessions involving a sample of 4-5 children of the same age who have undergone general anesthesia, and supplement data with individual interviews with children as needed. The interview guide will be developed to engage children in the conversation (13). All interviews will be recorded and transcribed. 4 Questionnaire Design: Based on insights from the interviews important themes and phrases will be translated into questions and answers on a pictorial questionnaire, incorporating the identified dimensions. Pilot testing and validation: Face validity of the questionnaire will be tested on 2-3 children through either in-person or telephone interviews and adjustments will be made if deemed necessary. After the adjustments, the questionnaire will be pilot tested on a group of 20 children, to validate if the questionnaire captures the children´s experiences according to the 7 dimensions of the WaPEF. The questionnaire will be administered on paper and data will be entered into REDCap. Inclusion criteria/ exclusion criteria/ setting: same as study 1. Data analysis: Transcripts from focus group interviews will be analysed using thematic analysis aligned with the 7 generic dimensions of WaPEF (14). Through collaborative efforts, the team will formulate consistent codes, subsequently applying them to the remaining two focus group transcripts using deductive coding. A comprehensive discussion within the research team will ascertain if the seven dimensions adequately encompass all emerging themes, resolving any discrepancies. Iterative modifications to the coding process will be made to ensure thorough coverage and prevent the oversight of any dimensions.
Expected papers
- Translation and adaption of the PedSQoR for Danish children aged 4-12
- Childrens experiences of surgery and anaesthesia. A focus group study
- Development of a Pediatric Patient-Reported Experience Measurement Instrument for children aged 4-12 undergoing anesthesia and surgery Research ethics Given their vulnerability in research, children necessitate careful consideration to ensure the study neither harms nor burdens them, weighing this against the study's significance in empowering children's voices. Therefore, specialized communication strategies will be employed in interactions with children. All interviews will be carried out by the PhD student who is a highly experienced nurse anesthetist with long experience in communication with children. Informed written consent will be sought from both parents and children. The study does not mandate approval from the Scientific Ethics Committee but will be registered on the Region Central Denmark's list of research projects.
5
Organization of the project The project will be conducted at Gødstrup Hospital, with Anne Højager Nielsen Ph.D., MCN, Associate Professor serving as the main supervisor.
Co-supervisors: Veronica Pisinger Ph.D. and researcher at the National Institute of Public Health; Denmark has special insight into the validation of questionnaires. Associate Professor and nurse anesthetist Pether Jildenståhl from Lunds University, Sweden has special insight into anaesthesia and children's needs and rights.
Collaborators: A/Prof Paul Lee-Archer, BMedSci, MBBS, FANZCA, MMed(ClinEpi), PhD, Senior Staff Specialist, Anaesthesia, Queensland Children's Hospital, Associate Professor, Faculty of Medicine, University of Queensland, and Professor Andrew Davidson FAHMS, Medical Director, Melbourne Childrens Trail Centre, Murdoch Children Research Institute,will host the international research stay.
Pediatric anesthetists and staff at Gødstrup Hospital. The PhD student: Draft of the protocol, data collection, data management, and data analysis.
The manuscripts will be drafted by the Ph.D. student, who will be the primary author of all publications. The PhD student will present research findings at conferences and international events. The PhD student will disseminate Relevant results to patient organizations and the public.
Study design
- Observational model
- Cohort
- Time perspective
- Prospective
- Number of arms
- 1
| Arm | Type | Receives |
|---|---|---|
| Children age 4-12, undergoing surgery and general anesthesia | – | – |
Who may qualify
- Ages
- 4 to 12 years
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Child
- Study population
- Children undergoing surgery and general anesthesia aged 4-12 years.
Key inclusion criteria (3 listed)
- Pediatric patients aged 4-12, American Society of
- Anesthesiologists physical status classification (ASA) I-III
- undergoing surgery
Key exclusion criteria (3 listed)
- Children with cognitive or sensory disorders
- children or parents who do not speak Danish,
- patients for whom there is no consent to participate.
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Primary outcome
To validate the Danish version of the PedSQoR in children aged 4-12.
Time frame: From enrollment to the end of week 4 after surgery
To pilot-test and adjust the questionnaire on a group of children aged 4-12 who have undergone surgery and anaesthesia
Time frame: From enrollment to 4 weeks after surgery
Patient Reported Experience Measure (PREM)
Results and safety
This study is still under way. Results are not available in the source record yet.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 10 Sep 2026.
- Individual participant dataSharing planned: Undecided
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part.
Anne Højager Nielsen, Ph.D. contact
3 sites in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
An observational study of Pediatric Anesthesia and Pediatric Surgery, run by Gødstrup Hospital at 3 sites in Denmark.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 3 inclusion and 3 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: looking for participants now, as of the sponsor's last update on 10 Sep 2026. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 3 sites in Denmark. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
This study is still under way. Results are not available in the source record yet.
How can a doctor refer a patient or contact the research team?
Contact Johanna Arnbjørn C Arnbjørn (+4527141475, johkoc@rm.dk), or a site near the patient. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
To validate the Danish version of the PedSQoR in children aged 4-12. (time frame: From enrollment to the end of week 4 after surgery). The study lists 2 primary outcomes in all. It is what the study was designed to measure, not a finding.
Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 10 Sep 2026.