An In-Hospital Family Member Cardiopulmonary Resuscitation (CPR) Education Program

Sponsor
University of Pennsylvania (Other)
Overall Status
Completed
CT.gov ID
NCT01260441
Collaborator
American Heart Association (Other)
500
3
2
60
166.7
2.8

Study Details

Study Description

Brief Summary

Each year in the United States, 300,000 people suffer from a Cardiac Arrest (CA), and of them, there is a 90% mortality rate. Out-of-Hospital arrests, in particular, have a 1-5% survival to hospital discharge. High quality CPR is crucial to lowering the mortality rate and increasing survival, yet only 15-30% of out-of-hospital CA victims receive bystander CPR. Studies have shown that prompt administration of CPR dramatically improves outcomes. In a recent study from Switzerland, lay bystander CPR doubled the survival rate at one month. Our study will look to train family members of at-risk cardiac patients in the skills of CPR through the American Heart Association's (AHA) CPR Anytime Friends and Family Personal Learning Program (CPR Anytime) to see if these family members are able to learn and perform quality CPR in the event that their family member should suffer a cardiac arrest.

Condition or Disease Intervention/Treatment Phase
  • Other: CPR Training using the Family and Friends CPR Anytime VSI Kit
Phase 1

Detailed Description

Using the AHA's CPR Anytime kit, we will work with family members of patients at high risk for a CA to learn lifesaving CPR skills. We will modify the AHA CPR video using the new AHA recommendations for bystanders which suggests doing chest compression only CPR. Using the original AHA video and our modified chest compression only video, we will randomize family members of patients at high risk for CA to one of these groups. Our research assistants will also be blinded to which video these subjects will be watching. After watching the video, we will have the subjects perform CPR on a mannequin using a CPR recording device that records chest compression rate and depth. We will follow up with the family members at 3 months, 6 months and 12 months to see if they retained their CPR knowledge and skills and to see if they had been in a situation where their CPR skills were needed and assess whether they performed their skills or not. We will also measure the number of people with whom the subjects shared their CPR Anytime kits-a quantity known as the multiplier effect to determine if they had shared the CPR Anytime kit with their family and friends, thereby increasing the possible number of lay persons trained in CPR and in turn able to perform bystander CPR if needed.

Study Design

Study Type:
Interventional
Actual Enrollment :
500 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Single (Participant)
Primary Purpose:
Prevention
Official Title:
CPR Education of Patient Family Members Using CPR Anytime Training Program
Study Start Date :
Oct 1, 2007
Actual Primary Completion Date :
Oct 1, 2012
Actual Study Completion Date :
Oct 1, 2012

Arms and Interventions

Arm Intervention/Treatment
Active Comparator: Standard CPR

Individuals will learn the Standard form of CPR (30:2, compressions:breathes) Main data points being collected over various increments are: 1) Comfort Level with using CPR 2) Secondary Training "multiplier effect" and 3) CPR Skills

Other: CPR Training using the Family and Friends CPR Anytime VSI Kit
Subjects will be trained using the American Heart Association's Family and Friends CPR Anytime Kit. Subjects will undergo training in-hospital and will be encouraged to take the kit home to share with their family members and friends.
Other Names:
  • Family and Friends CPR Anytime
  • American Heart Association Family and Friends CPR Anytime
  • CPR Anytime Video Self Instruction (VSI)
  • Active Comparator: Chest Compressions Only CPR

    Individuals will learn the chest compression only form of CPR (no rescue breathes) Main data points being collected at various increments are: 1) Comfort Level with using CPR 2) Secondary Training "multiplier effect" and 3) CPR Skills

    Other: CPR Training using the Family and Friends CPR Anytime VSI Kit
    Subjects will be trained using the American Heart Association's Family and Friends CPR Anytime Kit. Subjects will undergo training in-hospital and will be encouraged to take the kit home to share with their family members and friends.
    Other Names:
  • Family and Friends CPR Anytime
  • American Heart Association Family and Friends CPR Anytime
  • CPR Anytime Video Self Instruction (VSI)
  • Outcome Measures

    Primary Outcome Measures

    1. Subject Self-Confidence [within 30 minutes of CPR training]

      We will administer a comprehensive post-training likert scale scoring survey to measure the subject's comfort level using their newly acquired CPR skills.

    2. Secondary Training [3 month increments over a 12 month period of time]

      In addition, we will administer a telephone survey to measure the subject's secondary training through the CPR Anytime Kit.

    Secondary Outcome Measures

    1. Assessing CPR Skills [3 to 6 months post-training]

      We will assess the subject's CPR skills by administering a 2-minute simulated CPR skills check recorded on a Laerdal Skillreporter ResusciAnne mannequin and video camera. The skills check will be conducted initially post training and at the 3-, 6-, and 12-month time frame.

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years and Older
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    Yes
    Inclusion Criteria:
    • Family member's of patients with known coronary disease or cardiovascular risk factors, such as history of diabetes and hypertension.
    Exclusion Criteria:
    • If someone is physically unable to undergo CPR Training

    • Someone who has received CPR training in the past 2 years

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Hospital of the University of Pennsylvania Philadelphia Pennsylvania United States 19104
    2 Penn Presbyterian Medical Center Philadelphia Pennsylvania United States 19104
    3 Pennsylvania Hospital Philadelphia Pennsylvania United States 19106

    Sponsors and Collaborators

    • University of Pennsylvania
    • American Heart Association

    Investigators

    • Principal Investigator: Benjamin S Abella, MD, MPhil, University of Pennsylvania

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    University of Pennsylvania
    ClinicalTrials.gov Identifier:
    NCT01260441
    Other Study ID Numbers:
    • CRS-807120
    First Posted:
    Dec 15, 2010
    Last Update Posted:
    Nov 1, 2018
    Last Verified:
    Oct 1, 2018
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Nov 1, 2018