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Enrolling by invitation NCT07160881

Effectiveness of CPR Pillow

No phase Interventional Healthy Participants

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: Pillow maniquin training.
Who it may be relevant to
Registry conditions: Healthy Participants. Basic parameters: from 18 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
Turkey (Türkiye)
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →

Unsure about the terms? Read our patient guide →

Official title

Is There a More Affordable Method for Training in Cardiopulmonary Resuscitation - CPR? Comparing the Effectiveness of Standard CPR Manikins and CPR Pillows.

Overview

Pillows can be used to facilitate safe and effective learning and as a cheaper and more accessible alternative to manikins or computer-based methods for CPR training by non-healthcare professionals. The purpose of this study was to compare the effectiveness of pillows and manikins in CPR training.

Interventions

  • Behavioral Pillow maniquin training
    In this initiative, participants will be trained with a low-cost mannequin in addition to standard training.

Primary outcome measures

  • Cardiac compression number [Time frame: 0. day (The parameter will be evaluated immediately after my ethics.)]
  • Compression depth [Time frame: 0. day (The parameter will be evaluated immediately after training.)]
  • Hand Position [Time frame: 0. day (The parameter will be evaluated immediately after training.)]

Eligibility criteria

Inclusion criteria

  • Being over 18 years of age

Exclusion criteria

  • No physical impairment is required to perform CPR.

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: Yes

Study design

Allocation
N/A
Model
Single group
Masking
Open label
Primary purpose
Supportive care

Study locations

Turkey (Türkiye) · 1 center
  • Istanbul Beykent University — Istanbul

Identifiers

NCT: NCT07160881 · İstanbul Beykent Üniversitesi

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗