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Assessment of Chest Compression Depth Obtained Using the Smartphone Application as an Educational Tool With New Attachment Device

Assessment of Chest Compression Depth Obtained Using the Smartphone Application as an Educational Tool With New Attachment Device

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02964832
Enrollment
50
Registered
2016-11-16
Start date
2017-01-31
Completion date
2017-06-30
Last updated
2016-11-16

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Basic Cardiac Life Support

Keywords

Basic Cardiac Life Support, Education, Feedback

Brief summary

To improve the quality of CPR education, we want to assess the validity and reliability of the feedback depth measured by smartphone applications according to the smartphone attachment sites as an educational tool. However, in the prior study, armband method showed overestimated chest compression depth. The reason of the overestimation was analyzed that the weight of the smartphone amplified the inertial force to produce additional linear movement. In this study, we will make new device to fix the smartphone on the arm and on the hand and compare the chest compression depth between CPR manikin and smartphone application.

Interventions

DEVICEGrasp method
DEVICEArmband-in-hand method
DEVICEArmband-on-arm method

Sponsors

Soonchunhyang University Hospital
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
DIAGNOSTIC
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

* BLS provider or instructor

Exclusion criteria

* one who has physical problem in chest compression

Design outcomes

Primary

MeasureTime frame
Assessment of validity of Chest compression depth by smartphone application,PocketCPRThrough study completion, average 4 weeks

Contacts

Primary ContactJoonbum Park, MD, PhD
jesumania@gmail.com82-2-709-9117

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026