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

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18+
SponsorAkdeniz University

About this trial

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.

Eligibility criteria

This trial accepts healthy volunteers

Qualifiers

Age ≥ 18 years

Pediatric resident/assistant physician working in the Department of Pediatrics (Akdeniz University) with valid ÇİYAD certification

Willing and able to provide written informed consent

Able to perform a 2-minute continuous chest-compression CPR cycle on a pediatric manikin

Disqualifiers

Known chronic cardiopulmonary disease that may limit physical exertion during CPR

Known musculoskeletal disorder or chronic condition that may affect CPR performance

Acute injury/illness at the time of participation that could impair safe CPR performance

Refusal or inability to provide informed consent

Trial design

Design model

Crossover

Treatments tested in this trial

  • Fixed Standard Bed Height (58 cm)

    Other intervention

    Hospital bed height is set to a fixed standard height of 58 cm for the CPR session.

  • Anthropometry-Based Bed Height (Patella Midpoint)

    Other intervention

    Hospital bed height is adjusted to the participant's patella midpoint reference before the CPR session.

  • Anthropometry-Based Bed Height (Lower One-Third Patella-ASIS)

    Other intervention

    Hospital bed height is adjusted to the lower one-third point of the distance between the patella and ASIS before the CPR session.

  • Self-Selected Bed Height

    Other intervention

    Participant selects the bed height they perceive as optimal/comfortable prior to the CPR session.

Treatment groups

25 Participants
are divided into 4 treatment groups
Group A: Fixed Standard Bed Height (58 cm)Experimental treatment 1 intervention
Group B: Anthropometry-Based Bed Height (Patella Midpoint)Experimental treatment 1 intervention
Group C: Anthropometry-Based Bed Height (Lower One-Third of Patella-ASIS Distance)Experimental treatment 1 intervention
Group D: Self-Selected Bed HeightExperimental treatment 1 intervention

Trial outcomes

Primary outcomes

1

Correct chest compression depth (%, QCPR-defined)

Percentage of compressions meeting the target depth criteria as calculated by Laerdal Little Junior QCPR manikin sensors. (Recorded separately for each bed-height condition.)

Time frame
During each 2-minute chest compression-only CPR session (per bed-height condition).

Secondary outcomes

1

Average chest compression depth (mm)

Mean compression depth (mm) recorded by the QCPR manikin.

Time frame
During each 2-minute chest compression-only CPR session (per bed-height condition).
2

Average chest compression rate (compressions/min)

Mean compression rate (compressions/min) recorded by the QCPR manikin.

Time frame
During each 2-minute chest compression-only CPR session (per bed-height condition).
3

Correct chest recoil / release (%, QCPR-defined)

ercentage of compressions with complete release (recoil) as calculated by the QCPR manikin.

Time frame
During each 2-minute chest compression-only CPR session (per bed-height condition).
4

Perceived exertion (Borg RPE score)

Borg scale score collected verbally at the end of each CPR cycle.

Time frame
Immediately after each 2-minute CPR session.

Other outcomes

Sponsors and contacts

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