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

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

Status
Not yet recruiting
Phases
Unknown
Study type
Interventional
Source
ANZCTR
Registry ID
ACTRN12625001105437
Acronym
RESCUE-OB2 (RESuscitation Chest compression Upgrade Evaluation in patients with OBesity 2)
Enrollment
60
Registered
2025-10-10
Start date
2025-11-01
Completion date
2028-12-29
Last updated
2025-10-20

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 nurses 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 01.10.2025 to 12.2028.

Interventions

A total of 60 nurses 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 nurses 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. N

A total of 60 nurses 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 nurses 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. Nurses will perform CPR under the following three randomized conditions: - Standard CPR on a normal-weight manikin placed on the floor - CPR on an obese manikin placed on a hospital bed adjusted to its lowest position - CPR on an obese manikin placed on a hospital bed adjusted to its lowest position, with the nurse standing on a 10-cm platform to improve 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 hospital 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 nurse in hospital. 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: Feb 4, 2026