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NCT02175563 Clinical Trial

Tilt Cardiopulmonary Resuscitation With a Feedback Device

Cardiopulmonary Resuscitation Clinical Trial

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT02175563
Other study ID # Tilt CPR
Secondary ID
Status Completed
Phase N/A
First received June 25, 2014
Last updated August 25, 2014
Start date August 2014
Est. completion date August 2014

Study information
Verified date August 2014
Source Hanyang University
Contact n/a
Is FDA regulated No
Health authority Korea: Institutional Review Board
Study type Interventional

Clinical Trial Summary

According to the European Resuscitation Council (ERC) Guidelines for patient to a depth of approximately 5-6 cm on a firm and flat surface when possible. However, Cardiopulmonary resuscitation (CPR) performers may need to continue the chest Resuscitation 2010, CPR performers should compress the sternum of a compression in an oblique direction, such as in elevators. For a pregnant patient in cardiac arrest, the 2010 ERC Guidelines recommend that the performer place the patient in a left-lateral tilt of 15 - 30° using a firm wedge to support the pelvis and thorax because the pregnant uterus can compress the inferior vena cava. We hypothesized Smartphone based chest compression feedback app would improves quality of CPR in an angulated surface.

Recruitment information / eligibility
Status Completed
Enrollment 36
Est. completion date August 2014
Est. primary completion date August 2014
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Both
Age group 18 Years to 65 Years
Eligibility Inclusion Criteria:

- Healthy person

- > 18 years old

- Basic life support educated person

Exclusion Criteria:

- Cardiovascular disease

- Musculoskeletal disease

- Psychiatric disease

- Pregnant

- > 65 years old

Study Design

Allocation: Randomized, Intervention Model: Parallel Assignment, Masking: Single Blind (Outcomes Assessor), Primary Purpose: Basic Science

Related Conditions & MeSH terms

Intervention

Device:
• Audiovisual feedback from smartphone based app

Locations
Country Name City State
Korea, Republic of Hanyang University, College of medicine Seoul

Sponsors (1)
Lead Sponsor Collaborator
Hanyang University

Country where clinical trial is conducted

Korea, Republic of, 

Outcome
Type Measure Description Time frame Safety issue
Primary Chest compression depth To measure chest compression depth during 2 minutes within the first 30 days after the end of recording No
Primary Chest compression rate To measure the chest compression rate during 2 minutes within the first 30 days after the end of recording No
Secondary Accurate chest compression To measure the percentage of accurate chest compressions (i.e. correct depth, hand position, and recoil) of total chest compressions during 2 minutes within the first 30 days after the end of recording No
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