- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07239206
Serious Game for Improving Targeted Temperature Management Knowledge and Situational Awareness in Critical Care Nurses
Effectiveness of Serious Game on Facilitating Targeted Temperature Management Knowledge and Situational Awareness Among Critical Care Nurses
Study Overview
Status
Intervention / Treatment
Detailed Description
Targeted temperature management (TTM) is an evidence-based neuroprotective strategy recommended for patients resuscitated after cardiac arrest. Despite its clinical importance, critical care nurses often lack sufficient knowledge and situational awareness to effectively implement TTM, due to limited exposure to relevant cases and time constraints in training. Conventional teaching methods, while beneficial, face challenges such as limited resources, time, and opportunities for repeated practice.
Serious games, which integrate educational content with interactive digital game elements, offer a flexible and engaging learning tool that enables repeated practice in a safe, simulated environment. Previous studies have shown that serious games can enhance learners' motivation, knowledge retention, and decision-making skills.
This study will develop and implement a serious game specifically designed for TTM education. The randomized controlled trial will enroll 120 intensive care unit nurses, randomly allocated into two groups: the control group will receive lecture-based teaching with case discussion, while the experimental group will receive the same content supplemented with the serious game for additional practice. All participants will complete a pre-test, a post-test one week after the intervention, and a follow-up test at six weeks.
The primary outcome will be the improvement in TTM knowledge, and secondary outcomes will include situational awareness and system usability (experimental group only). The study is expected to provide evidence that serious games are an effective and scalable strategy for enhancing TTM-related knowledge and situational awareness, thereby supporting better quality of post-resuscitation care and patient safety.
Study Type
Enrollment (Estimated)
Phase
- Not Applicable
Contacts and Locations
Study Contact
- Name: HUI-YI LI
- Phone Number: 0920867591
- Email: bicky05@ntuh.gov.tw
Study Locations
-
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Taipei
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Taipei, Taipei, Taiwan, 100
- Recruiting
- National Taiwan University Hospital
-
Contact:
- Hui Yi Li, RN
- Phone Number: 886-920-868-591
- Email: bicky05@ntuh.gov.tw
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- Registered nurses currently working in adult intensive care units (medical, surgical, or mixed ICUs).
- Able to read and understand Chinese.
- Willing to participate and provide informed consent.
- Available to complete pre-test, post-test, and follow-up assessments.
Exclusion Criteria:
- Nurses working in pediatric or neonatal ICUs.
- Nurses holding administrative or supervisory positions (non-clinical).
- Nurses currently participating in other TTM-related educational or research programs.
- Individuals unable to complete the intervention or evaluation schedule.
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 |
|---|---|
|
Experimental: Experimental: Serious Game + Lecture
Participants in this arm will receive lecture-based teaching combined with a digital serious game designed to enhance targeted temperature management (TTM) knowledge and situational awareness.
The serious game includes interactive case scenarios, decision-making tasks, and real-time feedback to simulate ICU situations and reinforce learning.
|
A digital serious game designed to train critical care nurses in targeted temperature management (TTM).
The game features case-based simulations, interactive decision-making, and real-time feedback to improve clinical reasoning and situational awareness.
Standard lecture-based teaching covering the principles, procedures, and nursing care of targeted temperature management (TTM).
Participants in this group do not receive the serious game component.
|
|
Active Comparator: Active Comparator: Lecture Only
Participants in this arm will receive lecture-based teaching with case discussion only, covering the same targeted temperature management (TTM) content as the experimental group.
No serious game intervention will be provided.
|
Standard lecture-based teaching covering the principles, procedures, and nursing care of targeted temperature management (TTM).
Participants in this group do not receive the serious game component.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
System Usability Scale (SUS) Score
Time Frame: 1 week after intervention (experimental group only)
|
The usability of the serious game will be evaluated using the 10-item System Usability Scale (SUS).
Scores range from 0 to 100, with higher scores indicating better system usability and learner satisfaction.
|
1 week after intervention (experimental group only)
|
|
Change in Targeted Temperature Management (TTM) Knowledge Score
Time Frame: Baseline (pre-test), 1 week after intervention, and 6 weeks after intervention
|
TTM knowledge will be assessed using a validated 16-item multiple-choice questionnaire developed based on current clinical guidelines.
Scores range from 0 to 100, with higher scores indicating greater knowledge of targeted temperature management principles and nursing care.
|
Baseline (pre-test), 1 week after intervention, and 6 weeks after intervention
|
|
Change in Situational Awareness (SA) Score
Time Frame: Baseline, 1 week after intervention, and 6 weeks after intervention
|
Situational awareness will be measured using a 11-item Likert scale (1-5) questionnaire assessing perception, comprehension, and projection dimensions.
Total scores range from 12 to 60, with higher scores indicating greater situational awareness in clinical TTM scenarios.
|
Baseline, 1 week after intervention, and 6 weeks after intervention
|
Collaborators and Investigators
Publications and helpful links
General Publications
- Nolan JP, Morley PT, Vanden Hoek TL, Hickey RW, Kloeck WG, Billi J, Bottiger BW, Morley PT, Nolan JP, Okada K, Reyes C, Shuster M, Steen PA, Weil MH, Wenzel V, Hickey RW, Carli P, Vanden Hoek TL, Atkins D; International Liaison Committee on Resuscitation. Therapeutic hypothermia after cardiac arrest: an advisory statement by the advanced life support task force of the International Liaison Committee on Resuscitation. Circulation. 2003 Jul 8;108(1):118-21. doi: 10.1161/01.CIR.0000079019.02601.90. No abstract available.
- Nolan JP, Sandroni C, Bottiger BW, Cariou A, Cronberg T, Friberg H, Genbrugge C, Haywood K, Lilja G, Moulaert VRM, Nikolaou N, Olasveengen TM, Skrifvars MB, Taccone F, Soar J. European Resuscitation Council and European Society of Intensive Care Medicine guidelines 2021: post-resuscitation care. Intensive Care Med. 2021 Apr;47(4):369-421. doi: 10.1007/s00134-021-06368-4. Epub 2021 Mar 25.
- Gorbanev I, Agudelo-Londono S, Gonzalez RA, Cortes A, Pomares A, Delgadillo V, Yepes FJ, Munoz O. A systematic review of serious games in medical education: quality of evidence and pedagogical strategy. Med Educ Online. 2018 Dec;23(1):1438718. doi: 10.1080/10872981.2018.1438718.
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Estimated)
Study Completion (Estimated)
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
- 202507084RINA
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
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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