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BLS CompetenceNCT06624449

The Effect of Immediate Versus Delayed Debriefing on Basic Life Support Competence In Undergraduate Nursing Students.

A study testing Cold debriefing and Hot Debriefing in people with BLS Competence and Debriefing, run by University of Cincinnati at 1 site in United States.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial summary

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. Read more about this study

Who is it for?
Ages 18 years and olderHealthy volunteers can take part
Conditions the study is for
BLS Competence, Debriefing
What is being tested?
Cold debriefing and Hot Debriefing
Could I receive a placebo?
No, everyone receives an active treatment
How many people
44 participants
Where
1 siteUnited States
Study dates
29 Aug 2023to 7 Mar 2024
Phase
Interventional
Are there results?
Yes, posted in the registrySummary in the doctors' view

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 18 years and older
  • All sexes
  • Healthy volunteers accepted
  • Adult, Older adult

Who may be able to join

  • Junior or senior nursing students (i.e., in their third or fourth year of the BSN degree).

Who cannot join

  • Nursing students who are not junior or senior.

Trial locations and contacts

1 site in 1 country.

United States1 site
  • University Of Cincinnati College of Nursing

    Cincinnati, Ohio, 45221

Other trials in United States

About this study

Official title: 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.
Read the 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.

Being tested
Cold debriefing, Hot Debriefing
Keywords
Debriefing, Simulation, Basic Life Support, Undergraduate Nursing Students

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Cold debriefingBehavioural

    Manipulation (experimental): The researcher assigned a cold debriefing (after one-day post-simulation) for undergraduate nursing students in the intervention group.

  • Hot DebriefingBehavioural

    The control group received a hot debriefing (immediately after the simulation).

Study groups in NCT06624449
Study groupRoleWhat they receive
Cold DebriefingExperimentalThe researcher assigned a cold debriefing (after one-day post-simulation) for undergraduate nursing students in the intervention group.
Receives: Behavioral: Cold debriefing
Hot DebriefingOtherThe control group received a hot debriefing (immediately after the simulation).
Receives: Behavioral: Hot Debriefing

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Basic Life Support Competence

    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.

    Measured: Immediately after the intervention

Secondary outcomes (1)
  1. Debriefing Experience Scale

    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.

    Measured: Immediately after the intervention

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted3 Oct 2024
  2. Study start29 Aug 2023
  3. Primary completion7 Mar 2024
  4. Study completion7 Mar 2024

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Other
Allocation
Randomised
Intervention model
Parallel groups
Masking
Single blind
Who is masked
Participant
Enrolment
44 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT06624449
Sponsor's protocol ID
2023-0423
Status last verified
Nov 2024
First submitted
27 Sep 2024
Last updated
29 Nov 2024
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
Yes: All collected IPD, all IPD that underlie results in a publication

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.

    PubMed 36503623
  • 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.

    PubMed 33634592
  • 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.

    PubMed 25455910
  • Couper K, Perkins GD. Debriefing after resuscitation. Curr Opin Crit Care. 2013 Jun;19(3):188-94. doi: 10.1097/MCC.0b013e32835f58aa.

    PubMed 23426138

Questions about this trial

What is this clinical trial studying?

A study testing Cold debriefing and Hot Debriefing in people with BLS Competence and Debriefing, run by University of Cincinnati at 1 site in United States.

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 1 inclusion and 1 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 29 Nov 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 United States. 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?

Yes. Results are posted in the registry (first posted 29 Nov 2024). A summary is in the For doctors view, and the full results are on ClinicalTrials.gov.

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?

Basic Life Support Competence (time frame: Immediately after the intervention). It is what the study was designed to measure, not a finding.

Where can I read the original study information?

On the ClinicalTrials.gov record for NCT06624449, which also lists 6 linked publications.

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 29 Nov 2024.

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