NCT00570609

Brief Summary

This is a prospective study of 7th grade students participating in the CPR Anytime® program. After consent, participants will be asked to complete the program with their parent(s)/legal guardian(s) and encouraged to include other friends and family members in the program. After completing the program, the participant and their parent(s) will be evaluated for adequacy of chest compressions/CPR. The student participants will be evaluated again at 6 months for adequacy of chest compressions/CPR Objectives:

  1. 1.To evaluate 7th grade students for adequacy of CPR and chest compressions after completing a take home CPR course
  2. 2.To evaluate the multiplier effect of students training in CPR with their parents/family members using a take home CPR instructional kit
  3. 3.To evaluate the participating parent for adequacy of CPR and chest compressions after completing a take home CPR course
  4. 4.7th grade students can be trained, using CPR Anytime®, to perform adequate chest compressions/CPR and their skills will be maintained at 6 months
  5. 5.As part of the multiplier effect, an additional 1.5 family members per participant will be trained to perform adequate chest compressions/CPR

Trial Health

87
On Track

Trial Health Score

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

Enrollment
8

participants targeted

Target at below P25 for not_applicable

Timeline
Completed

Started Jan 2008

Typical duration for not_applicable

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

December 10, 2007

Completed
1 day until next milestone

First Posted

Study publicly available on registry

December 11, 2007

Completed
21 days until next milestone

Study Start

First participant enrolled

January 1, 2008

Completed
1.9 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

December 1, 2009

Completed
6 months until next milestone

Study Completion

Last participant's last visit for all outcomes

June 1, 2010

Completed
Last Updated

April 26, 2012

Status Verified

April 1, 2012

Enrollment Period

1.9 years

First QC Date

December 10, 2007

Last Update Submit

April 25, 2012

Conditions

Keywords

CPR

Outcome Measures

Primary Outcomes (1)

  • As tested by a CPR instructor, 7th grade students will be evaluated for performance of adequate chest compressions/CPR initially and at at 6 months after training with CPR Anytime®,

    6 months

Secondary Outcomes (1)

  • As part of the multiplier effect, an additional 1.5 family members per participant will be expected to be trained to perform adequate chest compressions/CPR

    6 months

Study Arms (1)

CPR Anytime

EXPERIMENTAL

Participants will be asked to complete the program with their parent(s)/legal guardian(s) and encouraged to include other friends and family members in the program

Other: CPR Anytime education

Interventions

After consent, participants will be asked to complete the 22 minute DVD CPR Anytime program with their parent(s)/legal guardian(s) and encouraged to include other friends and family members in the program

CPR Anytime

Eligibility Criteria

Sexall
Healthy VolunteersNo
Age GroupsChild (0-17), Adult (18-64), Older Adult (65+)

You may qualify if:

  • Participants
  • Access to home DVD player
  • Participants must be able to read, speak and understand English

You may not qualify if:

  • Lack of functioning home DVD player
  • Physical limitation to the ability to perform CPR/Chest compressions

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Salisbury Middle School

Allentown, Pennsylvania, 18103, United States

Location

MeSH Terms

Conditions

Coronary Artery Disease

Condition Hierarchy (Ancestors)

Coronary DiseaseMyocardial IschemiaHeart DiseasesCardiovascular DiseasesArteriosclerosisArterial Occlusive DiseasesVascular Diseases

Study Officials

  • Marna R Greenberg, D.O., MPH

    LVH

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
interventional
Phase
not applicable
Allocation
NA
Masking
NONE
Purpose
PREVENTION
Intervention Model
SINGLE GROUP
Sponsor Type
OTHER
Responsible Party
SPONSOR INVESTIGATOR
PI Title
Director of Emergency Medicine Research

Study Record Dates

First Submitted

December 10, 2007

First Posted

December 11, 2007

Study Start

January 1, 2008

Primary Completion

December 1, 2009

Study Completion

June 1, 2010

Last Updated

April 26, 2012

Record last verified: 2012-04

Locations