Child HealthNCT06077578
Understanding the Perceptions, Behavior, and Attitudes Towards Hospital Play Services
An observational study of Child Health, run by Chinese University of Hong Kong at 1 site in Hong Kong.
Trial summary
Aim This proposed study aims to investigate the perceptions, behavior, and attitudes of healthcare professionals, previously hospitalized children, and parents of these children toward hospital play services in the Hong Kong healthcare system. Read more about this study
- Who is it for?
- Any ageHealthy volunteers can take part
- Conditions the study is for
- Child Health
- How many people
- 210 participants
- Where
- 1 siteHong Kong
- Study dates
- 6 Nov 2023to 30 May 2024
- Phase
- Observational
- Are there results?
- None posted in the registry
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 Any age
- All sexes
- Healthy volunteers accepted
- Child, Adult, Older adult
Study population: 182 healthcare professionals will be recruited in the pediatric units of six acute care public hospitals from different regions of Hong Kong. 14 children previously admitted to hospitals, and their parents, will be recruited in Hong Kong.
Who may be able to join
- be aged 18 or above
- be able to read and understand English
- be healthcare professionals, including nurses, physicians, physiotherapists, occupational therapists, and radiotherapists, have at least one year experience in caring for hospitalized children
- be aged under 18
- be able to communicate in Cantonese
- be previously hospitalized and had received hospital play service provided by hospital play specialists
Show all 9Show fewer
- be aged 18 or above
- be able to communicate in Cantonese
- his/her children be previously hospitalized and had received hospital play service provided by hospital play specialists
Who cannot join
- psychologically or physically unable to communicate
- Previously hospitalized children
- psychologically or physically unable to communicate
- Parents
- psychologically or physically unable to communicate
Trial locations and contacts
1 site in 1 country.
About this study
Official title: Understanding the Perceptions, Behavior, and Attitudes of Healthcare Professionals, Hospitalized Children, and Parents of These Children Toward Hospital Play Services
Aim This proposed study aims to investigate the perceptions, behavior, and attitudes of healthcare professionals, previously hospitalized children, and parents of these children toward hospital play services in the Hong Kong healthcare system. In addition, in-depth interviews will be conducted with selected participants to investigate their views on the role of hospital play specialists , as well as the sustainability and development of hospital play specialists services in Hong Kong hospitals
Study Design A mixed-methods (quantitative and qualitative) approach will be used to collect data. The study will be divided into two phases. In Phase I, a cross-sectional study, using a structured questionnaire, will be conducted on healthcare professionals in the pediatric units of six acute care public hospitals from different regions of Hong Kong. In Phase II, in-depth semi-structured interviews will be conducted with randomly selected healthcare professionals who have participated in the Phase I study. In addition, the investigators will collect feedback and comments from previously hospitalized children and their parents.
Read the detailed description
- Phase I study A retrospective cross-sectional questionnaire will be administered to the healthcare professionals who work in the abovementioned public hospitals. A convenience sample of 182 healthcare professionals will be recruited. In addition, the investigators will contact professional pediatric organizations, such as the Hong Kong Pediatric Society and Hong Kong College of Pediatric Nursing to help invite healthcare professionals to participate in this research.
A structured questionnaire has been developed based on existing international and/or local literature. The information gathered will include perceptions of and attitudes toward hospital play, the feasibility and usefulness of hospital play, understanding the roles and responsibilities of hospital play specialists , perceptions of collaborating with hospital play specialists , and perceptions of the need for hospital play services in Hong Kong hospital settings. In addition, demographic information, including age, gender, occupation, and years of experience in taking care of hospitalized children, will be documented.
Data Analysis for the Phase I Study Data analysis will be performed using SPSS Statistics for Windows, V.26.0 (IBM). Continuous variables with normal distribution will be presented as the mean and standard deviation, and those with non-normal distribution will be presented as the median. Categorical variables will be presented as the frequency and proportion.
ii) Phase II Study A semi-structured interview will be conducted with randomly selected healthcare professionals who have participated in the Phase I study. A semi-structured interview guide will be developed by the research team, which includes a professor with extensive knowledge of and experience in conducting both quantitative and qualitative research related to pediatric patients and hospital play activities and a team of experts working in Playright with extensive experience in conducting hospital play interventions for hospitalized children. The interview guide will be further assessed for its relevancy and wording appropriateness by two advanced practice nurses working in Children's Hospital with extensive experience in providing care for hospitalized children.
A purposive sample of 20 healthcare professionals randomly selected from the Phase I study and 14 children previously admitted to hospitals, and their parents, will be recruited for the interviews. However, the actual sample size will depend on data saturation. A one-to-one audiotaped semi-structured in-depth interview will then be conducted with each participant until data saturation is achieved. Each interview will last approximately 20 to 30 minutes. During each interview, a research assistant will act as the interviewer to facilitate the informants to freely express their feelings, thoughts, and ideas. Another research assistant will act as an observer to document all non-verbal cues of the informants.
Data Analysis for the Phase II Study After conducting the interviews, the recordings will be fully transcribed, verbatim, in Cantonese to capture the nuances of expression unique to the dialect, and selected quotations relevant to the themes will subsequently be translated into English. During the coding process, two researchers will be responsible for analyzing the narratives. The analyses will begin with an intensive examination of the transcripts to search for general constructs and themes. Special attention will be given to constructs that diverge from the major topics framed by the guiding questions. The transcripts will first be coded using the open coding method. Details in the interview conversations will then be closely examined to extract a large number of initial categories. As the number of codes increases, some closely related codes will be merged, resulting in a smaller, more manageable set of codes. Selective coding will then be adopted to code the transcripts using the established categories. To facilitate the data analysis process, meetings will be held to discuss emergent themes. During the coding process, any inconsistencies in the interpretation of quotations or the assignment of codes will be resolved through discussions with the research team members. Finally, a complete set of codes will be generated to facilitate comparisons and the development of themes and categories. To achieve a more coherent and logical structure, the themes and categories will be modified by breaking down complicated concepts, merging similar ones, and rearranging certain themes and categories based on their relationships. The analyses will be performed using NVivo Version 9 (QSR International Pty Ltd., 2010).
To ensure data credibility, the interviewer will first ask iterative questions and use probes during the interviews. Second, debriefing sessions will be held between the research assistants and the principal investigator after every five interviews. Modifications will be made by the principal investigator according to the developing ideas and interpretations. Third, data analysis will be performed by two researchers independently, and field notes will be taken into account during the analysis. Regular research team meetings will be held to resolve any disagreements that may arise. The informants will also be invited to review the transcripts and clarify the meaning of their statements, if required. To increase the transferability of the findings, the study will be conducted in acute care hospitals from different regions in Hong Kong. Purposive sampling will be adopted to maximize sample variation, which will help the investigators to obtain a representative group of informants for the interviews. To ensure the confirmability and dependability of the findings, an audit trail will be maintained by another experienced researcher who is not part of this research team. She will review a collection of documents to attest to the interpretations of the researchers.
- Conditions
- Child Health
- Keywords
- hospital play services, healthcare professionals, hospitalized children, parents
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 |
|---|---|---|
| Healthcare professionals | Healthcare professionals, including nurses, physicians, physiotherapists, occupational therapists, and radiotherapists, have at least one year experience in caring for hospitalized children will be recruited. | |
| Previously hospitalized children | Previously hospitalized children who had received a hospital play service provided by hospital play specialists. | |
| parents | Parents of previously hospitalized children who had received a hospital play service provided by hospital play specialists. |
What is being measured
The primary outcome is the main question the study is designed to answer.
Perceptions, behavior, and attitudes
The perceptions, behavior, and attitudes of healthcare professionals, previously hospitalized children, and parents of these children toward hospital play services will be investigated by semi-structured in-depth interviews
Measured: baseline
Secondary outcomes (4)
Perceptions of feasibility and usefulness
Perceptions of feasibility and usefulness of healthcare professionals towards hospital play services will be investigated by a structured questionnaire
Measured: baseline
understanding the roles and responsibilities of hospital play specialists
Perceived understanding of healthcare professionals towards the roles and responsibilities of hospital play specialists will be investigated by a structured questionnaire
Measured: baseline
Perceptions of collaborating with hospital play specialists
Perceptions of collaborating with hospital play specialists of healthcare professionals will be be investigated by a structured questionnaire
Measured: baseline
Perceptions of the need for hospital play services in Hong Kong hospital settings
Perceptions of the need for hospital play services in Hong Kong hospital settings of healthcare professionals will be be investigated by a structured questionnaire
Measured: baseline
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted11 Oct 2023
- Study start6 Nov 2023
- Primary completion30 May 2024
- Study completion30 May 2024
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Child HealthStudies of the same condition, open and under way.
- More trials run by Chinese University of Hong KongThe sponsor's other registered studies.
- 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
- Cross-sectional
- Enrolment
- 210 participants (actual)
Sponsor and investigators
- Lead sponsor
- Chinese University of Hong Kong
- Sponsor type
- University, hospital or other
- Responsible party
- Principal investigator, Li Ho Cheung William, Chinese University of Hong Kong
- Investigators
- Ho Cheung William Li, Principal investigator, williamli@cuhk.edu.hk
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT06077578
- Sponsor's protocol ID
- HPS
- Status last verified
- Aug 2024
- First submitted
- 5 Oct 2023
- Last updated
- 28 Aug 2024
- Results posted
- No
- Data monitoring committee
- Yes
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- Yes: The relevant anonymized patient level data, full dataset, technical appendix, and statistical code are available on reasonable request. The approval from the Principal Investigator for the purpose of data use is required.
Study at a glance
From the registry record, last updated by the sponsor on 28 Aug 2024. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Understanding the Perceptions, Behavior, and Attitudes of Healthcare Professionals, Hospitalized Children, and Parents of These Children Toward Hospital Play Services
- ClinicalTrials.gov ID
- NCT06077578
- Acronym / sponsor ID
- HPS
- Conditions
- Child Health
- Keywords
- hospital play services, healthcare professionals, hospitalized children, parents
- Study type
- Observational
- Recruitment status
- Completed
- Enrolment
- 210 participants (actual)
- Lead sponsor
- Chinese University of Hong KongUniversity, hospital or other
- Study start
- 6 Nov 2023 (actual)
- Primary completion
- 30 May 2024 (actual)
- Study completion
- 30 May 2024 (actual)
- First posted
- 11 Oct 2023 (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.
Aim This proposed study aims to investigate the perceptions, behavior, and attitudes of healthcare professionals, previously hospitalized children, and parents of these children toward hospital play services in the Hong Kong healthcare system. In addition, in-depth interviews will be conducted with selected participants to investigate their views on the role of hospital play specialists , as well as the sustainability and development of hospital play specialists services in Hong Kong hospitals
Study Design A mixed-methods (quantitative and qualitative) approach will be used to collect data. The study will be divided into two phases. In Phase I, a cross-sectional study, using a structured questionnaire, will be conducted on healthcare professionals in the pediatric units of six acute care public hospitals from different regions of Hong Kong. In Phase II, in-depth semi-structured interviews will be conducted with randomly selected healthcare professionals who have participated in the Phase I study. In addition, the investigators will collect feedback and comments from previously hospitalized children and their parents.
Detailed description
- Phase I study A retrospective cross-sectional questionnaire will be administered to the healthcare professionals who work in the abovementioned public hospitals. A convenience sample of 182 healthcare professionals will be recruited. In addition, the investigators will contact professional pediatric organizations, such as the Hong Kong Pediatric Society and Hong Kong College of Pediatric Nursing to help invite healthcare professionals to participate in this research.
A structured questionnaire has been developed based on existing international and/or local literature. The information gathered will include perceptions of and attitudes toward hospital play, the feasibility and usefulness of hospital play, understanding the roles and responsibilities of hospital play specialists , perceptions of collaborating with hospital play specialists , and perceptions of the need for hospital play services in Hong Kong hospital settings. In addition, demographic information, including age, gender, occupation, and years of experience in taking care of hospitalized children, will be documented.
Data Analysis for the Phase I Study Data analysis will be performed using SPSS Statistics for Windows, V.26.0 (IBM). Continuous variables with normal distribution will be presented as the mean and standard deviation, and those with non-normal distribution will be presented as the median. Categorical variables will be presented as the frequency and proportion.
ii) Phase II Study A semi-structured interview will be conducted with randomly selected healthcare professionals who have participated in the Phase I study. A semi-structured interview guide will be developed by the research team, which includes a professor with extensive knowledge of and experience in conducting both quantitative and qualitative research related to pediatric patients and hospital play activities and a team of experts working in Playright with extensive experience in conducting hospital play interventions for hospitalized children. The interview guide will be further assessed for its relevancy and wording appropriateness by two advanced practice nurses working in Children's Hospital with extensive experience in providing care for hospitalized children.
A purposive sample of 20 healthcare professionals randomly selected from the Phase I study and 14 children previously admitted to hospitals, and their parents, will be recruited for the interviews. However, the actual sample size will depend on data saturation. A one-to-one audiotaped semi-structured in-depth interview will then be conducted with each participant until data saturation is achieved. Each interview will last approximately 20 to 30 minutes. During each interview, a research assistant will act as the interviewer to facilitate the informants to freely express their feelings, thoughts, and ideas. Another research assistant will act as an observer to document all non-verbal cues of the informants.
Data Analysis for the Phase II Study After conducting the interviews, the recordings will be fully transcribed, verbatim, in Cantonese to capture the nuances of expression unique to the dialect, and selected quotations relevant to the themes will subsequently be translated into English. During the coding process, two researchers will be responsible for analyzing the narratives. The analyses will begin with an intensive examination of the transcripts to search for general constructs and themes. Special attention will be given to constructs that diverge from the major topics framed by the guiding questions. The transcripts will first be coded using the open coding method. Details in the interview conversations will then be closely examined to extract a large number of initial categories. As the number of codes increases, some closely related codes will be merged, resulting in a smaller, more manageable set of codes. Selective coding will then be adopted to code the transcripts using the established categories. To facilitate the data analysis process, meetings will be held to discuss emergent themes. During the coding process, any inconsistencies in the interpretation of quotations or the assignment of codes will be resolved through discussions with the research team members. Finally, a complete set of codes will be generated to facilitate comparisons and the development of themes and categories. To achieve a more coherent and logical structure, the themes and categories will be modified by breaking down complicated concepts, merging similar ones, and rearranging certain themes and categories based on their relationships. The analyses will be performed using NVivo Version 9 (QSR International Pty Ltd., 2010).
To ensure data credibility, the interviewer will first ask iterative questions and use probes during the interviews. Second, debriefing sessions will be held between the research assistants and the principal investigator after every five interviews. Modifications will be made by the principal investigator according to the developing ideas and interpretations. Third, data analysis will be performed by two researchers independently, and field notes will be taken into account during the analysis. Regular research team meetings will be held to resolve any disagreements that may arise. The informants will also be invited to review the transcripts and clarify the meaning of their statements, if required. To increase the transferability of the findings, the study will be conducted in acute care hospitals from different regions in Hong Kong. Purposive sampling will be adopted to maximize sample variation, which will help the investigators to obtain a representative group of informants for the interviews. To ensure the confirmability and dependability of the findings, an audit trail will be maintained by another experienced researcher who is not part of this research team. She will review a collection of documents to attest to the interpretations of the researchers.
Study design
- Observational model
- Cohort
- Time perspective
- Cross-sectional
- Number of arms
- 3
| Arm | Type | Receives |
|---|---|---|
| Healthcare professionals | – | –Healthcare professionals, including nurses, physicians, physiotherapists, occupational therapists, and radiotherapists, have at least one year experience in caring for hospitalized children will be recruited. |
| Previously hospitalized children | – | –Previously hospitalized children who had received a hospital play service provided by hospital play specialists. |
| parents | – | –Parents of previously hospitalized children who had received a hospital play service provided by hospital play specialists. |
Who may qualify
- Sex
- All
- Healthy volunteers
- Accepted
- Age groups
- Child, Adult, Older adult
- Study population
- 182 healthcare professionals will be recruited in the pediatric units of six acute care public hospitals from different regions of Hong Kong. 14 children previously admitted to hospitals, and their parents, will be recruited in Hong Kong.
Key inclusion criteria (9 listed)
- be aged 18 or above
- be able to read and understand English
- be healthcare professionals, including nurses, physicians, physiotherapists, occupational therapists, and radiotherapists, have at least one year experience in caring for hospitalized children
- be aged under 18
- be able to communicate in Cantonese
Key exclusion criteria (5 listed)
- psychologically or physically unable to communicate
- Previously hospitalized children
- psychologically or physically unable to communicate
- Parents
- psychologically or physically unable to communicate
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
Perceptions, behavior, and attitudes
Time frame: baseline
The perceptions, behavior, and attitudes of healthcare professionals, previously hospitalized children, and parents of these children toward hospital play services will be investigated by semi-structured in-depth interviews
4 secondary outcomes
Perceptions of feasibility and usefulness
Time frame: baseline
understanding the roles and responsibilities of hospital play specialists
Time frame: baseline
Perceptions of collaborating with hospital play specialists
Time frame: baseline
Perceptions of the need for hospital play services in Hong Kong hospital settings
Time frame: baseline
Results and safety
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 28 Aug 2024.
- Individual participant dataSharing planned: Yes. The relevant anonymized patient level data, full dataset, technical appendix, and statistical code are available on reasonable request. The approval from the Principal Investigator for the purpose of data use is required.
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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. This study is not recruiting at the moment.
Ho Cheung William Li principal investigator
williamli@cuhk.edu.hk
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
An observational study of Child Health, run by Chinese University of Hong Kong at 1 site in Hong Kong.
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 9 inclusion and 5 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: finished, as of the sponsor's last update on 28 Aug 2024. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 1 site in Hong Kong. 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?
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
How can a doctor refer a patient or contact the research team?
The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Perceptions, behavior, and attitudes (time frame: baseline). 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 28 Aug 2024.