Simulation study in ward conditions before and after use of CPR feedback device

In-situ simulation for assessment of CPR feedback device use for BLS skills in trained CPR providers: A pre-post intervention study - NIL

Status

Active, not recruiting

Phases

Phase 4

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2025/05/087095

Enrollment

Registered

2025-05-20

Start date

Unknown

Completion date

Unknown

Last updated

2025-05-26

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

None listed

Interventions

Intervention1: Use of real time feedback device for BLS skills in trained CPR providers: This will be a pre-post intervention study, in which all the participants will participate in CPR code on a man

Eligibility

Inclusion criteria

Inclusion criteria: 1. Experienced CPR providers (Resident doctors, nurses, technicians etc) who have undergone a structured CPR training program. 2. Participants willing to take part in the study

Exclusion criteria

Exclusion criteria: 1. Participant refusal 2. Inability to perform CPR on mannequin for continuous 2 minutes.

Design outcomes

Primary

Measure	Time frame
To evaluate compliance with ideal CPR compression metrics with the help of composite CPR variable â??Excellent CPR ? defined as achieving at least 90% compliance with the chest compression depth, rate of compression and chest recoil before and after the introduction of real time feedback device for each participant.Timepoint: The participants will be evaluated during the simulation exercise on the day of conduct of the exercise.	—

Measure

Time frame

To evaluate compliance with ideal CPR compression metrics with the help of composite CPR variable â??Excellent CPR ? defined as achieving at least 90% compliance with the chest compression depth, rate of compression and chest recoil before and after the introduction of real time feedback device for each participant.Timepoint: The participants will be evaluated during the simulation exercise on the day of conduct of the exercise.

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Secondary

Measure	Time frame
Percentage of chest compressions compliant with AHA high quality chest compression metrics in the study.Timepoint: The participants will be evaluated during the simulation exercise on the day of conduct of the exercise.;The participants subjective satisfaction score of the usefulness of realtime feedback on fivepoint Likert scale.Timepoint: The participants will be evaluated during the simulation exercise on the day of conduct of the exercise.;The participants ease of use score on five-point Likert scale.Timepoint: The participants will be evaluated during the simulation exercise on the day of conduct of the exercise.;To calculate chest compression fraction.Timepoint: The participants will be evaluated during the simulation exercise on the day of conduct of the exercise.	—

Measure

Time frame

Percentage of chest compressions compliant with AHA high quality chest compression metrics in the study.Timepoint: The participants will be evaluated during the simulation exercise on the day of conduct of the exercise.;The participants subjective satisfaction score of the usefulness of realtime feedback on fivepoint Likert scale.Timepoint: The participants will be evaluated during the simulation exercise on the day of conduct of the exercise.;The participants ease of use score on five-point Likert scale.Timepoint: The participants will be evaluated during the simulation exercise on the day of conduct of the exercise.;To calculate chest compression fraction.Timepoint: The participants will be evaluated during the simulation exercise on the day of conduct of the exercise.

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Countries

India

Contacts

Public ContactAMIT Kumar

AIIMS, New Delhi

amit2007kr@gmail.com8055087505

Outcome results