- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06624449
The Effect of Immediate Versus Delayed Debriefing on Basic Life Support Competence In Undergraduate Nursing Students.
The Effect of Hot and Cold Debriefing on BLS Competence and Reflection In Undergraduate Nursing Students.
The goal of this clinical trial is to find out if immediate (hot) or delayed (cold) debriefing is better for undergraduate nursing students during Basic Life Support (BLS) training.
The study aims to:
- Identify the effect of hot versus cold debriefing in BLS training for nursing students.
- Identify which debriefing method students prefer.
Researchers will compare the two debriefing methods. Participants will:
- Be randomly assigned (by flipping a coin) to either hot or cold debriefing.
- Take part in a simulation about Basic Life Support.
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
This RCT aimed to identify the efficacy of cold versus hot debriefing in BLS training for undergraduate nursing students' BLS competence and to assess the impact of hot and cold debriefing nursing students' debriefing experience.
Specific Aims/Hypothesis Specific aim 1: Identify the efficacy of cold versus hot debriefing in BLS training for undergraduate nursing students' BLS competence.
Hypothesis 1a: In both cold and hot debriefing groups, there is a significant difference in the BLS competence of undergraduate nursing students between pre-intervention and post-intervention.
Hypothesis 1b: Undergraduate nursing students who receive cold debriefing will show greater BLS competence than those who receive hot debriefing. Our approach to testing the aim is to conduct an experimental design study.
Specific aim 2: Assess the impact of hot and cold debriefing on undergraduate nursing students' debriefing experience.
Hypothesis 2: Undergraduate nursing students who receive cold debriefing will show greater debriefing experience scores than those who receive hot debriefing.
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
Ohio
-
Cincinnati, Ohio, United States, 45221
- University of Cincinnati College of Nursing
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- Junior or senior nursing students (i.e., in their third or fourth year of the BSN degree).
Exclusion Criteria:
- Nursing students who are not junior or senior.
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: Cold Debriefing
The researcher assigned a cold debriefing (after one-day post-simulation) for undergraduate nursing students in the intervention group.
|
Manipulation (experimental): The researcher assigned a cold debriefing (after one-day post-simulation) for undergraduate nursing students in the intervention group.
|
|
Other: Hot Debriefing
The control group received a hot debriefing (immediately after the simulation).
|
The control group received a hot debriefing (immediately after the simulation).
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Basic Life Support Competence
Time Frame: Immediately after the intervention
|
Competence level was measured via the American Heart Association (2020) Basic Life Support competency checklist, which is a dichotomous rating scale of 0 (not done/done incorrectly) and 1 (done correctly); there was a total of 15 points.
The higher the score, the better the outcome.
|
Immediately after the intervention
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Debriefing Experience Scale
Time Frame: Immediately after the intervention
|
The Debriefing Experience Scale (DES) (Reed, 2012) was developed to assess nursing students debriefing experience.
It included 20 elements in total and was split into four subscales: (1) Analyzing Thoughts and Feelings; (2) Learning and Makin Connections; (3) Facilitator Skill in Conducting the Debriefing; and (4) Appropriate Facilitator Guidance (Reed, 2012).
A Likert scale ranges from 1 (strongly disagree) to 5 (strongly agree).
The minimum score is 20 and the maximum is 100.
The higher the score, the better the outcome.
|
Immediately after the intervention
|
Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Fahad Alanezi, PhD Candidate, MSc, BSN, University of Cincinnati
Publications and helpful links
General Publications
- Kolb, D. A. (2014). Experiential learning: Experience as the source of learning and development (2nd ed.). Pearson Education, Inc.
- Reed, S. J. (2012). Debriefing experience scale: Development of a tool to evaluate the student learning experience in debriefing. Clinical Simulation in Nursing, 8(6), e211-e217.
- Meguerdichian M, Bajaj K, Ivanhoe R, Lin Y, Sloma A, de Roche A, Altonen B, Bentley S, Cheng A, Walker K. Impact of the PEARLS Healthcare Debriefing cognitive aid on facilitator cognitive load, workload, and debriefing quality: a pilot study. Adv Simul (Lond). 2022 Dec 12;7(1):40. doi: 10.1186/s41077-022-00236-x.
- Ha EH. Effects of hot and cold debriefing in simulation with case-based learning. Jpn J Nurs Sci. 2021 Feb 26:e12410. doi: 10.1111/jjns.12410. Online ahead of print.
- Kessler DO, Cheng A, Mullan PC. Debriefing in the emergency department after clinical events: a practical guide. Ann Emerg Med. 2015 Jun;65(6):690-8. doi: 10.1016/j.annemergmed.2014.10.019. Epub 2014 Nov 15.
- Couper K, Perkins GD. Debriefing after resuscitation. Curr Opin Crit Care. 2013 Jun;19(3):188-94. doi: 10.1097/MCC.0b013e32835f58aa.
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
Other Study ID Numbers
- 2023-0423
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
IPD Plan Description
IPD Sharing Time Frame
IPD Sharing Supporting Information Type
- STUDY_PROTOCOL
- SAP
- ICF
- ANALYTIC_CODE
- CSR
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
product manufactured in and exported from the U.S.
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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