Data from: The influence of real-time feedback on the quality of resuscitation: a prospective study comparing bystanders, paramedic course participants, and emergency physician trainee
Data files
Nov 18, 2025 version files 82.95 KB
-
DataTable_Manuscript_comparisonProfession_GMS_281124_SKK.csv
76.60 KB
-
README.md
6.35 KB
Abstract
The aim of this study was to analyze the potential benefits of real-time feedback in resuscitation training for participants in the prehospital emergency chain and to compare differences in the quality of chest compressions (CC) with and without feedback. The primary endpoint was to analyze the proportion of CC achieving the recommended depth (5-6cm) and frequency (100-120 / min) during two minutes of CC. This prospective cohort study compares bystanders (N = 75), paramedic trainees (N = 75), and emergency physician trainees (N = 75) with and without the feedback system of the Zoll X-Series®. Without feedback, paramedics (P) achieved the target compression frequency in 82.7 %, bystanders (B) in 49.8 % and emergency physician trainees (EP) in 75% (P vs. B, p < 0.001; EP vs. P, p = 0.759; EP vs. B, p = 0,217). There were no significant differences in target compression depth without feedback. With feedback, P achieved the compression frequency in 90.7%, B in 72.8% and EP in 91.4% (P vs. B, p < 0.001; EP vs. P, p = 0.425; EP vs. B, p < 0.001. With feedback, P achieved the compression depth in 56.9%, B in 47.3 % and EP in 75.1 % (P vs. B, p = 0.759; EP vs. P, p = 0.217; EP vs. B, p = 0.002). The results underscore the importance of real-time feedback in emergency medical training, especially for B. All cohorts showed significant improvement, indicating that feedback enhances CC and promotes skill development. Given the importance of high-quality CC, their early optimization in the training is essential. This highlights the need for standardized training concepts, including timing recommendations for feedback systems. Future studies should consider real-life pre-hospital conditions and investigate chest compression to validate transferability to real-life scenarios.
Description of the data and file structure
This dataset contains quantitative performance data on chest compressions (CC) obtained from a prospective cohort study conducted at the state-recognized emergency medical service school “NAW Berlin.” The study investigated whether real-time feedback improves resuscitation quality across three participant groups: bystanders, paramedic course participants, and emergency physician trainees.
Each of the 225 participants performed two standardized 2-minute chest compression trials on a resuscitation simulator (AmbuMan®) with a real-time feedback system (Zoll X-Series®):
- One trial without feedback (WoF)
- One trial with feedback (WF)
Both trials were performed under identical, standardized conditions. The feedback system displayed and recorded compression depth and frequency; chest recoil was visible on the monitor but not exportable by the evaluation software (RescueNet Code Review). The study focused on depth (cm) and rate (compressions per minute) as the key quality indicators according to European Resuscitation Council (ERC) Guidelines 2021.
Ethical approval was obtained from the Brandenburg Medical School Ethics Committee (E-01-20200403). All participants provided written informed consent prior to participation.
Files and variables
File: DataTable_Manuscript_comparisonProfession_GMS_281124_SKK.csv
Description: The dataset includes 225 anonymized participant records, one per row. Each record contains two performance trials (with and without feedback), including mean values, counts, and percentages of compressions within and outside target ranges.
Variables
- participant: Anonymous participant ID
- age: Age in years
- sex: Biological Sex (1 = male, 2 = female)
- group: B = Bystander, P = Paramedic Course Participant, EP = Emergency Physician Trainee
- @2m_WoF_D_CompressionFraction: 2 minute trial without feedback depth compression fraction
- @2m_WoF_D_DepthAverage: 2 minute trial without feedback depth average
- @2m_WoF_D_Total_CC: 2 minute trial without feedback depth total chest compressions
- @2m_WoF_D_DepthTarget: 2 minute trial without feedback depth target (5-6 cm)
- @2m_WoF_D_DepthTargetPercent: 2 minute trial without feedback depth target in percent
- @2m_WoF_D_DepthAboveTarget: 2 minute trial without feedback depth above target (> 6 cm)
- @2m_WoF_D_DepthAbovePercent: 2 minute trial without feedback depth above in percent
- @2m_WoF_D_DepthBelowTarget: 2 minute trial without feedback depth below target (< 5 cm)
- @2m_WoF_D_DepthBelowPercent: 2 minute trial without feedback depth below in percent
- @2m_WoF_D_DepthStandardDeviation: 2 minute trial without feedback depth standard deviation
- @2m_WoF_F_AverageFrequency: 2 minute trial without feedback average frequency
- @2m_WoF_F_FrequencyTarget: 2 minute trial without feedback frequency target (100-120 / min)
- @2m_WoF_F_FrequencyTargetPercent: 2 minute trial without feedback frequency target in percent
- @2m_WoF_F_FrequencyAboveTarget: 2 minute trial without feedback frequency above target (> 120 / min)
- @2m_WoF _F_FrequencyAbovePercent: 2 minute trial without feedback frequency above target in percent
- @2m_WoF_F_FrequencyBelowTarget: 2 minute trial without feedback frequency below target ( < 100 / min)
- @2m_WoF_F_FrequencyBelowPercent: 2 minute trial without feedback frequency below in percent
- @2m_WoF_F_FrequencyStandardDeviation: 2 minute trial without feedback frequency standard deviation
- @2m_WF_D_CompressionFraction: 2 minute trial with feedback depth compression fraction
- @2m_WF_D_AverageDepth: 2 minute trial with feedback depth average depth
- @2m_WF_D_Total_CC: 2 minute trial with feedback depth total chest compressions
- @2m_WF_D_DepthTarget: 2 minute trial with feedback depth target (5-6 cm)
- @2m_WF_D_DepthTargetPercent: 2 minute trial with feedback depth target in percent
- @2m_WF_D_DepthAboveTarget: 2 minute trial with feedback depth above target (> 6 cm)
- @2m_WF_D_DepthAbovePercent: 2 minute trial with feedback depth above percent
- @2m_WF_D_DepthBelowTarget: 2 minute trial with feedback depth below target (< 5 cm)
- @2m_WF_D_DepthBelowPercent: 2 minute trial with depth below target percent
- @2m_WF_D_DepthStandardDeviation: 2 minute trial with feedback depth standard deviation
- @2m_WF_F_AverageFrequency: 2 minute trial with feedback frequency average frequency
- @2m_WF_F_FrequencyTarget: 2 minute trial with feedback frequency target (100-120/min)
- @2m_WF_F_FrequencyTargetPercent: 2 minute trial with feedback frequency target percent
- @2m_WF_F_FrequencyAboveTarget: 2 minute trial with feedback frequency above target (> 120 / min)
- @2m_WF_F_FrequencyAbovePercent: 2 minute trial with feedback frequency above target percent
- @2m_WF_F_FrequencyBelowTarget: 2 minute trial with feedback frequency below target (< 100 / min)
- @2m_WF_F_FrequencyBelowPercent: 2 minute trial with feedback frequency below percent
- @2m_WF_F_FrequencyStandardDeviation: 2 minute trial with feedback frequency standard deviation
- agegroup1: four category age group: 1 = 16-20, 2 = 21-30, 3 = 31-40, 4 = 41-56
- agegroup2: three category age group: 1 = 16-25, 2 = 26-35, 3 = 36-56
- ageMedian: dichotomized age (1 = <28 years, 2 = >28 years)
- agegroup3: binary age split (1 = <30 years, 2 = >30 years)
- AG_B: age group Bystander
- AG_EP: age group emergency physician
- AG_P: age group paramedics
- Diff_WF_WoF_FreqTarg_p: Difference of with feedback and without feedback frequency target percent
- Diff_WF_WoF_DepTarg_p: Difference of with feedback and without feedback depth target percent
Note: comma used as decimal delimiter within .csv file
Code/software
Data analyses were conducted using:
- SPSS Version 28 (IBM)
- RescueNet Code Review (data extraction)
- Microsoft Excel / Word for Mac, Version 16.16.27
Access information
Other publicly accessible locations of the data:
- Data are only available in this Dryad repository
Data was derived from the following sources:
-
All data were collected prospectively as part of the study and were not derived from other sources.
*Study design
*The prospective cohort study was approved by the ethics committee of “Medizinische Hochschule Brandenburg” (E-01-20200403).
*Participants/study population
*The recruitment and data collection were conducted at the state-recognized emergency medical school in Berlin. A total of 225 participants from first aid classes (B), paramedic classes (P), and emergency classes for physicians (EP) voluntarily participated in the study outside of class hours. Before the start of the study, the B participants acquired theoretical knowledge on performing chest compressions (CC). At the time of data collection, the P cohort had completed four weeks of theoretical and practical instructions and was about to begin hospital and ambulance internships. The EP cohort consisted of licensed physicians participating in an emergency physician class.
*Study setting and procedure
*The resuscitation simulator AmbuMan® was equipped with the feedback system of the Zoll X-Series®. Initially participants performed a two-minute chest compression (CC) without the visibility of real-time feedback. After a break of two minutes, another CC for two minutes was performed, this time with real-time feedback.
*Data collection
*Data collection took place from October 2020 to January 2021. The focus of the resuscitation analysis was on evaluating the compression depth within the target range and the compression rate within the target. The reference values are specified by the resuscitation guidelines [5]. The compression depth should be between 5–6 cm. The compression rate should be between 100–120 compressions per minute [5]. "Above the target range" referred to compressions with a depth > 6 cm or a compression rate > 120 compressions per minute. "Below the target range" was defined as a compression depth of less than 5 cm or a compression rate < 100 compressions per minute.
*Analysis
*The evaluation of the results was conducted using the "RescueNet Code Review" program, which compares compression depth and rate with the specified guideline parameters. Statistical analysis of the collected data was performed using the statistical software SPSS Version 28 (IBM). To describe the central tendency in cases of uneven data distribution or ordinal data, the median with the 25th–75th percentile was used. The comparison of the three independent groups was performed using the Mann-Whitney U test, as the data were not parametrically distributed. Categorical variables were compared using the Chi-square test. The results are presented in tables and graphs as box plots or as absolute numbers with percentage shares.
