- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06431802
Construction and Application of the Visualization Training Platform Based on a Multimodal Standardized Dataset for Pain Assessment in Critically Ill Children
The goal of this clinical trial is to learn if the visualization training platform based on a multimodal standardized dataset for pain assessment in critically ill children is applicable for pain assessment training. The study aims to answer:
- Does pain assessment training with a visualization training platform based on a multimodal standardized dataset for pain assessment in critically ill children improve participants' knowledge level of pain assessment?
- Does pain assessment training with a visualization training platform based on a multimodal standardized dataset for pain assessment in critically ill children improve participants' skill level of pain assessment?
Researchers will compare a visualization training platform based on a multimodal standardized dataset for pain assessment in critically ill children to on-site lessons to see how well the platform intervention can be applied to pain assessment training.
Participants will:
- Use the visualization platform or receive on-site lessons for pain assessment training every week for 1 month.
- Test before and 1 month after the start of the study.
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
-
Shanghai, China
- Children's Hospital of Fudan University
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Child
- Adult
- Older Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- Obtain a Nurse Practitioner's Certificate;
- Nurses working in critical care;
- Voluntarily participate in this study.
Exclusion Criteria:
- Nurses in the neonatal unit (due to the specificity of pain assessment in neonates);
- Not on duty during the survey period due to further training, rotations, sick leave, maternity leave, etc.;
- Nurses who travel to our hospital for further training, rotations, or clinical placements during the survey period;
- Those who fail to complete the full intervention or withdrew from the study midway.
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Other
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Active Comparator: Conventional intervention group
On-site course training in pain assessment
|
A nursing specialist with extensive clinical and teaching experience will provide on-site course training.
The training will cover topics related to pain and pain assessment, such as: pain definition, types, physiological mechanisms, performance, pain assessment tools, and frequency of pain assessment.
Interventions will be provided once a week for 4 weeks.
|
|
Experimental: Platform intervention group
Pain assessment training using the visualization training platform based on a multimodal standardized dataset for pain assessment in critically ill children
|
Using a pre-assigned account to log in to the platform, read the guidance instructions and enter the platform to start training.
Basic knowledge of pain and pain assessment can be learnt through the Learning Resources module on the platform, and pain assessment training can be conducted through the Pain Assessment Exercise module.
During pain assessment training the platform provides instant feedback based on the participant's exercises.
Interventions will be completed in 4 weeks.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Knowledge level of pain assessment
Time Frame: baseline, 1st month since baseline
|
Use the Pediatric ICU Nurses' Pain Assessment Knowledge Test,which is measured on a scale from 0 to 100 points.
The higher the total score, the higher the level of knowledge.
|
baseline, 1st month since baseline
|
|
Skill level of pain assessment
Time Frame: baseline, 1st month since baseline
|
The pediatric pain assessment cases developed by the research team will be utilized for evaluation.
The correct percentage range is from 0% to 100%, with higher percentages indicating a higher skill level in pain assessment.
|
baseline, 1st month since baseline
|
Collaborators and Investigators
Investigators
- Study Director: Ying Gu, Doctor, Children's Hospital of Fudan University
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- FNF20231219
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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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