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Cardiac ArrestLower_limb_CPRNCT07646496

Comparison of Chest Compressions Performed With the Lower Limb and the Classical Method (Lower_limb_CPR).

A study testing Instruction to perform chest compressions using the lower limb (foot) in people with Cardiac Arrest, run by Marcin Muża at 1 site in Poland.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial summary

Chest compressions, alongside early defibrillation, are the most important component of basic life support for adults. High-quality compressions give the patient a chance to survive cardiac arrest. Read more about this study

Who is it for?
Any ageHealthy volunteers can take part
Conditions the study is for
Cardiac Arrest
What is being tested?
Instruction to perform chest compressions using the lower limb (foot)
Could I receive a placebo?
No, everyone receives an active treatment
How many people
99 participants
Where
1 sitePoland
Study dates
22 Nov 2025to 1 Jan 2026
Phase
Interventional
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages Any age
  • All sexes
  • Healthy volunteers accepted
  • Child, Adult, Older adult

Who may be able to join

  • Paramedic and nursing students from the Powiśle Academy of Applied Sciences who voluntarily and knowingly consent to participate in the study.
  • Completed first aid training during their studies.

Who cannot join

  • Lack of consent to participate in the study.
  • Education in another medical profession.

Trial locations and contacts

1 site in 1 country.

Poland1 site
  • Powiślańska Academy of Applied Sciences

    Kwidzyn, Pomeranian Voivodeship, 82-500

Other trials in Poland

About this study

Official title: Comparison of the Quality of Chest Compressions Performed With the Lower Limb and the Classical Method During Cardiopulmonary Resuscitation - a Simulation Study.

Chest compressions, alongside early defibrillation, are the most important component of basic life support for adults. High-quality compressions give the patient a chance to survive cardiac arrest.

The chest compression technique, described for years in guidelines, requires kneeling next to the victim and pressing down on the center of the chest with both extended arms at a specific rate and depth. However, there is a lack of scientific data on whether alternative compression methods (for example, using a lower limb) can be considered equally effective in situations where conventional compressions are impossible (e.g., the witness to cardiac arrest is a person with a disability, with an upper limb injury, or an elderly person; or when there is very little space to kneel). The aim of the study is to determine whether compressions performed with the dominant foot by paramedic and nursing students can be considered comparable in quality to conventional compressions. Furthermore, subjective levels of physical fatigue are assessed.

Read more

Participants are recruited from among paramedic and nursing students who voluntarily and knowingly consent to participate in the research study.

Inclusion Criteria

  • Paramedic and nursing students from the Powiśle Academy of Applied Sciences who voluntarily and knowingly consent to participate in the study.
  • Completed first aid training during their studies.

Exclusion Criteria

  • Lack of consent to participate in the study.
  • Education in another medical profession.

Procedure Students are randomly assigned to the control and study groups. Before participating in the simulation scenario, participants complete a questionnaire asking several demographic questions (age, gender, education, physical activity). Participants then enter the simulation room individually. The activities are not videotaped. From the moment of randomization, students are anonymous to the researcher. Both when completing the questionnaires and recording data from the simulation scenario, participants will be assigned a unique number (generated solely for the study), which prevents identification. Upon entering the simulation room, participants receive all instructions verbally. Students' task in the simulation environment involves performing two minutes of continuous chest compressions. Participants in the control group perform these compressions traditionally, while those in the study group are asked to perform compressions using their dominant leg. Compression quality is assessed using a Prestan Manikin (2000 series) with the CPR FEEDBACK mobile app. Parameters such as compression depth, rate, and relaxation are assessed. Completion of chest compressions on the manikin marks the end of the simulation scenario. Furthermore, participants are verbally questioned after the simulation about their level of physical fatigue on a scale of 1 (none) to 10 (the most severe ever).

Conditions
Cardiac Arrest
Being tested
Instruction to perform chest compressions using the lower limb (foot)
Keywords
cardiac arrest, chest compressions, CPR, resuscitation
Medical subject headings
Heart Arrest

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Instruction to perform chest compressions using the lower limb (foot)Other

    Verbal instruction to perform chest compressions using the lower limb (foot) before the simulation scenario.

Study groups in NCT07646496
Study groupRoleWhat they receive
StudyExperimentalNot described
Receives: Other: Instruction to perform chest compressions using the lower limb (foot)
ControlNo interventionNot described

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Chest compressions quality - Frequency

    Measured: 2 minutes

  2. Chest compressions quality - Relaxation

    Measured: 2 minutes

  3. Chest compressions quality - Depth

    Measured: 2 minutes

Secondary outcomes (1)
  1. Fatigue

    Self-assessed physical fatigue (1-10 scale)

    Measured: 2 minutes

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted12 Jun 2026
  2. Study start22 Nov 2025
  3. Primary completion1 Jan 2026
  4. Study completion1 Jan 2026

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Health services research
Allocation
Randomised
Intervention model
Parallel groups
Masking
None (open label)
Enrolment
99 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT07646496
Sponsor's protocol ID
Powiślańska1
Acronym
Lower_limb_CPR
Status last verified
Jun 2026
First submitted
4 Jun 2026
Last updated
12 Jun 2026
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
Undecided

Questions about this trial

What is this clinical trial studying?

A study testing Instruction to perform chest compressions using the lower limb (foot) in people with Cardiac Arrest, run by Marcin Muża at 1 site in Poland.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 2 inclusion and 2 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 12 Jun 2026. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in Poland. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Chest compressions quality - Frequency (time frame: 2 minutes). The study lists 3 primary outcomes in all. It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 12 Jun 2026.

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