Exploring the Application of Virtual Reality in Enhancing Chest Percussion Techniques, Reducing Caregiver Stress, and Improving Teaching Effectiveness for Caregivers of Children With Pneumonia
1 other identifier
interventional
60
1 country
1
Brief Summary
This study intends to adopt a Randomized Controlled Trial (RCT) design to explore the application of virtual reality in training chest percussion techniques for children with pneumonia. The aim is to evaluate the accuracy and efficiency of caregivers in performing this technique. The study will analyze the potential clinical benefits of improving caregivers' chest percussion skills and reducing caregiver stress
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P25-P50 for not_applicable
Started Feb 2025
Typical duration for not_applicable
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
February 7, 2025
CompletedFirst Submitted
Initial submission to the registry
June 24, 2025
CompletedFirst Posted
Study publicly available on registry
July 2, 2025
CompletedPrimary Completion
Last participant's last visit for primary outcome
March 30, 2026
CompletedStudy Completion
Last participant's last visit for all outcomes
March 30, 2027
ExpectedMay 5, 2026
May 1, 2026
1.1 years
June 24, 2025
May 3, 2026
Conditions
Outcome Measures
Primary Outcomes (2)
Pediatric Chest Physiotherapy Technique Assessment Form
An evaluation checklist consisting of nine items was developed in accordance with the nursing skills standards for pediatric chest physiotherapy
Participants will be assessed at two time points: on the day of hospital admission or transfer, and on the fourth day after the teaching intervention
Pediatric Chest Percussion Knowledge Assessment
includes ten items addressing percussion techniques and precautions, and evaluates caregivers' knowledge of the chest percussion process and safety considerations.
Participants will be assessed at two time points: on the day of hospital admission or transfer, and on the fourth day after the teaching intervention
Secondary Outcomes (3)
Caregiver Stress Self-Assessment Scale
Participants will be assessed at two time points: on the day of hospital admission or transfer, and on the fourth day after the teaching intervention
Respiratory Sounds of Pediatric Patients
Participants will be assessed at two time points: on the day of hospital admission or transfer, and on the fourth day after the teaching intervention
Learning Outcomes of Virtual Reality-Based Teaching Materials
Fourth day after virtual reality intervention
Study Arms (2)
Virtual Reality Chest Percussion Teaching Program
EXPERIMENTALParticipants will be assessed at two time points: on the day of hospital admission or transfer, and on the fourth day after the teaching intervention.
Nurse-Led Chest Percussion Health Education Program
NO INTERVENTIONParticipants will be assessed at two time points: on the day of hospital admission or transfer, and on the fourth day after the teaching intervention.
Interventions
Participants will be assessed at two time points: on the day of hospital admission or transfer, and on the fourth day after the teaching intervention.
Eligibility Criteria
You may qualify if:
- \- Primary caregivers of pediatric patients who have been diagnosed by a physician as requiring chest percussion as an adjunct therapy and are at least 18 years old
You may not qualify if:
- Severe communication barriers (inability to communicate in Mandarin or Taiwanese, blindness, or deafness) that prevent understanding of the simulator.
- Primary caregivers of pediatric patients with contraindications to chest percussion therapy, such as rib fractures, osteoporosis, tumors or skin graft sites, or pulmonary embolism.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Hui-Mei, Chen
Yuanlin, Taiwan
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- NONE
- Purpose
- PREVENTION
- Intervention Model
- CROSSOVER
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Head Nurse
Study Record Dates
First Submitted
June 24, 2025
First Posted
July 2, 2025
Study Start
February 7, 2025
Primary Completion
March 30, 2026
Study Completion (Estimated)
March 30, 2027
Last Updated
May 5, 2026
Record last verified: 2026-05
Data Sharing
- IPD Sharing
- Will not share
Patient privacy consideration