NCT02175563

Brief 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.

Trial Health

87
On Track

Trial Health Score

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

Enrollment
36

participants targeted

Target at P25-P50 for not_applicable

Timeline
Completed

Started Aug 2014

Geographic Reach
1 country

1 active site

Status
completed

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

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

June 25, 2014

Completed
1 day until next milestone

First Posted

Study publicly available on registry

June 26, 2014

Completed
1 month until next milestone

Study Start

First participant enrolled

August 1, 2014

Completed
Same day until next milestone

Primary Completion

Last participant's last visit for primary outcome

August 1, 2014

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

August 1, 2014

Completed
Last Updated

August 27, 2014

Status Verified

August 1, 2014

Enrollment Period

Same day

First QC Date

June 25, 2014

Last Update Submit

August 25, 2014

Conditions

Cardiopulmonary ResuscitationBasic Cardiac Life Support

Keywords

ChestCompression

Outcome Measures

Primary Outcomes (2)

  • Chest compression depth

    To measure chest compression depth during 2 minutes

    within the first 30 days after the end of recording

  • Chest compression rate

    To measure the chest compression rate during 2 minutes

    within the first 30 days after the end of recording

Secondary Outcomes (1)

  • Accurate chest compression

    within the first 30 days after the end of recording

Study Arms (2)

Without feedback

NO INTERVENTION

Participants compress the chest of the manikin without smartphone based feedback app.

With feedback

EXPERIMENTAL

Participants compress the chest of the manikin with a smartphone based feedback app.

Device: Audiovisual feedback from smartphone based app

Interventions

Audiovisual feedback from smartphone based appDEVICE
With feedback

Eligibility Criteria

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

You may qualify if:

  • Healthy person
  • \> 18 years old
  • Basic life support educated person

You may not qualify if:

  • Cardiovascular disease
  • Musculoskeletal disease
  • Psychiatric disease
  • Pregnant
  • \> 65 years old

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Hanyang University, College of medicine

Seoul, 133792, South Korea

Location

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
SINGLE
Who Masked
OUTCOMES ASSESSOR
Purpose
BASIC SCIENCE
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Department of Emergency Medicine

Study Record Dates

First Submitted

June 25, 2014

First Posted

June 26, 2014

Study Start

August 1, 2014

Primary Completion

August 1, 2014

Study Completion

August 1, 2014

Last Updated

August 27, 2014

Record last verified: 2014-08

Locations

KR(1)