NCT07329842

Brief Summary

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.

Trial Health

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Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Trial has exceeded expected completion date
Enrollment
25

participants targeted

Target at below P25 for not_applicable

Timeline
Completed

Started Sep 2025

Shorter than P25 for not_applicable

Geographic Reach
1 country

1 active site

Status
recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

Study Start

First participant enrolled

September 28, 2025

Completed
3 months until next milestone

First Submitted

Initial submission to the registry

December 29, 2025

Completed
11 days until next milestone

First Posted

Study publicly available on registry

January 9, 2026

Completed
23 days until next milestone

Primary Completion

Last participant's last visit for primary outcome

February 1, 2026

Completed
2 months until next milestone

Study Completion

Last participant's last visit for all outcomes

April 1, 2026

Completed
Last Updated

January 9, 2026

Status Verified

December 1, 2025

Enrollment Period

4 months

First QC Date

December 29, 2025

Last Update Submit

December 29, 2025

Conditions

Keywords

Cardiopulmonary ResuscitationCPR QualityPediatric Cardiac ArrestRescuer FatigueBed Height in CPR

Outcome Measures

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.)

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

Secondary Outcomes (7)

  • Average chest compression depth (mm)

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

  • Average chest compression rate (compressions/min)

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

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

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

  • Perceived exertion (Borg RPE score)

    Immediately after each 2-minute CPR session.

  • Change in heart rate (beats/min)

    From immediately before to immediately after each 2-minute CPR session.

  • +2 more secondary outcomes

Study Arms (4)

Fixed Standard Bed Height (58 cm)

EXPERIMENTAL

Participants perform 2 minutes of single-rescuer, chest-compression-only pediatric CPR on a manikin placed on a hospital bed set to a fixed standard height of 58 cm.

Other: Fixed Standard Bed Height (58 cm)

Anthropometry-Based Bed Height (Patella Midpoint)

EXPERIMENTAL

Participants perform 2 minutes of single-rescuer, chest-compression-only pediatric CPR on a manikin with the hospital bed height adjusted to the participant's patella midpoint (knee midpoint) reference.

Other: Anthropometry-Based Bed Height (Patella Midpoint)

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

EXPERIMENTAL

Participants perform 2 minutes of single-rescuer, chest-compression-only pediatric CPR on a manikin with the hospital bed height adjusted to the lower one-third point of the distance between the patella and the anterior superior iliac spine (ASIS).

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

Self-Selected Bed Height

EXPERIMENTAL

Participants perform 2 minutes of single-rescuer, chest-compression-only pediatric CPR on a manikin with the hospital bed height set to the participant's self-selected "most comfortable/optimal" height.

Other: Self-Selected Bed Height

Interventions

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

Fixed Standard Bed Height (58 cm)

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

Anthropometry-Based Bed Height (Patella Midpoint)

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

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

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

Self-Selected Bed Height

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • 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
  • Available to complete four CPR sessions (each at a different bed-height condition) on separate days

You may not qualify if:

  • 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

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

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

Antalya, Antalya, 07020, Turkey (Türkiye)

RECRUITING

Central Study Contacts

Ömür Akınel, Research Assistant

CONTACT

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
NONE
Masking Details
No masking; bed height condition is apparent to participants and study staff.
Purpose
OTHER
Intervention Model
CROSSOVER
Model Details: Randomized, within-subject 4-condition crossover simulation study. Each participant completes four separate sessions (on different days), performing 2 minutes of single-rescuer, chest-compression-only pediatric CPR per session. Bed height is set to one of four predefined conditions per session; the order of conditions is randomized for each participant.
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Research Assistant

Study Record Dates

First Submitted

December 29, 2025

First Posted

January 9, 2026

Study Start

September 28, 2025

Primary Completion

February 1, 2026

Study Completion

April 1, 2026

Last Updated

January 9, 2026

Record last verified: 2025-12

Data Sharing

IPD Sharing
Will not share

Locations