NCT02964832

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.

Trial Health

35
At Risk

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Trial has exceeded expected completion date
Enrollment
50

participants targeted

Target at P25-P50 for not_applicable

Timeline
Completed

Started Jan 2017

Shorter than P25 for not_applicable

Status
unknown

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

November 2, 2016

Completed
14 days until next milestone

First Posted

Study publicly available on registry

November 16, 2016

Completed
2 months until next milestone

Study Start

First participant enrolled

January 1, 2017

Completed
2 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

March 1, 2017

Completed
3 months until next milestone

Study Completion

Last participant's last visit for all outcomes

June 1, 2017

Completed
Last Updated

November 16, 2016

Status Verified

November 1, 2016

Enrollment Period

2 months

First QC Date

November 2, 2016

Last Update Submit

November 12, 2016

Conditions

Keywords

Basic Cardiac Life Support, Education, Feedback

Outcome Measures

Primary Outcomes (1)

  • Assessment of validity of Chest compression depth by smartphone application,PocketCPR

    Through study completion, average 4 weeks

Study Arms (3)

PocketCPR;Grasp method

ACTIVE COMPARATOR

Subject grasp a smartphone in the hand and compress the chest of manikin.

Device: Grasp method

PocketCPR;Armband-in-hand method

ACTIVE COMPARATOR

Grab the smartphone-contained-armband in hand when performing chest compression

Device: Armband-in-hand method

PocketCPR;Armband-on-arm method

ACTIVE COMPARATOR

Fix the smartphone-contained-armband on upperarm when performing chest compression

Device: Armband-on-arm method

Interventions

PocketCPR;Grasp method
PocketCPR;Armband-in-hand method
PocketCPR;Armband-on-arm method

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • BLS provider or instructor

You may not qualify if:

  • one who has physical problem in chest compression

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Central Study Contacts

Joonbum Park, MD, PhD

CONTACT

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
NONE
Purpose
DIAGNOSTIC
Intervention Model
CROSSOVER
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Assisstant professor of Emergency Medicine

Study Record Dates

First Submitted

November 2, 2016

First Posted

November 16, 2016

Study Start

January 1, 2017

Primary Completion

March 1, 2017

Study Completion

June 1, 2017

Last Updated

November 16, 2016

Record last verified: 2016-11