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Effectiveness of body position modifications during simulated CPR on chest compression quality in patients with obesity.

Effect of body position modifications on chest compression depth, rate and recoil during simulated cardiopulmonary resuscitation (CPR) in patients with obesity

Status
Not yet recruiting
Phases
Unknown
Study type
Interventional
Source
ANZCTR
Registry ID
ACTRN12625000658415
Acronym
RESCUE-OB (RESuscitation Chest compression Upgrade Evaluation in patients with OBesity)
Enrollment
60
Registered
2025-06-20
Start date
2025-06-23
Completion date
2028-12-29
Last updated
2025-09-08

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

Conditions

None listed

Brief summary

This is a randomized crossover trial assessing the effect of body positioning on CPR quality in simulated obese and non-obese patients. Sixty paramedics will perform chest compressions on manikins under three different ergonomic conditions. Primary outcomes include compression depth, rate, and full chest recoil, measured using the Laerdal QCPR Meter 2. The study has been approved by the Bioethics Committee of Wroclaw Medical University (KB 12/2025). It is scheduled to take place from 23 June 2025 to December 2028.

Interventions

A total of 60 paramedics will be included in this study. All participants will perform 2-minute chest compression (CPR) sessions on manikins simulating patients with and without obesity. Interventions involve modified body positioning to optimise compression mechanics. Each paramedic will perform compressions in both standard and modified positions in a randomized crossover design. CPR quality parameters (compression depth, rate, and full chest recoil) are measured using the Laerdal QCPR Meter 2

A total of 60 paramedics will be included in this study. All participants will perform 2-minute chest compression (CPR) sessions on manikins simulating patients with and without obesity. Interventions involve modified body positioning to optimise compression mechanics. Each paramedic will perform compressions in both standard and modified positions in a randomized crossover design. CPR quality parameters (compression depth, rate, and full chest recoil) are measured using the Laerdal QCPR Meter 2. 1. Paramedics will perform CPR in the following three randomized conditions: - Standard CPR on a manikin with normal body mass, placed on the floor - CPR on an obese manikin placed on the floor - CPR on an obese manikin placed on the floor, using a 10 cm knee pad to assist ergonomic positioning All compressions are performed without real-time feedback. A 3-minute rest is provided between sessions. Each participant will also complete a pre-test demographic questionnaire (age, sex, BMI, profession, CPR experience, etc.). All procedures are conducted at the Medical Simulation Centre and EMS training facilities under standardised supervision.

Sponsors

Wroclaw Medical University
Lead SponsorUniversity

Study design

Allocation
Randomised controlled trial
Intervention model
Crossover
Primary purpose
Educational / counselling / training
Masking
Open (masking not used)

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years
Healthy volunteers
No

Inclusion criteria

1. Currently working as a paramedic in EMS system. 2. At least 1 year of professional experience 3. No medical contraindications to performing CPR 4. Voluntary written informed consent

Exclusion criteria

1. Severe or acute cardiovascular, respiratory, or musculoskeletal disorders 2. Any health conditions that may impair safe or effective performance of chest compressions

Outcome results

None listed

Source: ANZCTR · Data processed: Aug 30, 2026