Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
Healthy Volunteers
NCT07329842

Effect of Bed Height on Chest Compression Quality and Provider Biomechanics During Pediatric CPR Simulation

Led by Akdeniz University · Updated on 2026-01-09

25

Participants Needed

1

Research Sites

26 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

High-quality chest compressions are critical for outcomes after pediatric cardiac arrest, yet rescuer ergonomics and bed height may adversely affect compression quality and fatigue. This randomized crossover simulation study will evaluate how four different bed-height settings influence pediatric CPR quality and rescuer biomechanics. Pediatric emergency medicine residents will perform 2-minute chest-compression-only CPR on a pediatric manikin placed on a hospital bed under four bed-height conditions in randomized order across separate sessions. CPR quality metrics from the manikin's feedback system, rescuer fatigue, physiologic responses, and arm angle over time will be compared to identify an ergonomically optimal bed-height approach.

CONDITIONS

Official Title

Effect of Bed Height on Chest Compression Quality and Provider Biomechanics During Pediatric CPR Simulation

Who Can Participate

Age: 18Years +
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Age 18 years or older
  • Pediatric resident or assistant physician working in the Department of Pediatrics at Akdeniz University with valid ÇİYAD certification
  • Willing and able to provide written informed consent
  • Able to perform 2 minutes of continuous chest-compression CPR on a pediatric manikin
  • Available to complete four CPR sessions at different bed-height conditions on separate days
Not Eligible

You will not qualify if you...

  • Known chronic cardiopulmonary disease limiting physical exertion during CPR
  • Known musculoskeletal disorder or chronic condition affecting CPR performance
  • Acute injury or illness at the time of participation impairing safe CPR performance
  • Refusal or inability to provide informed consent

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Akdeniz University Hospital / Faculty of Medicine Hospital - Dept. of Pediatrics

Antalya, Antalya, Turkey (Türkiye), 07020

Actively Recruiting

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Research Team

Ö

Ömür Akınel, Research Assistant

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

RANDOMIZED

Model

CROSSOVER

Primary Purpose

OTHER

Number of Arms

4

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