- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT00570869
Training Mothers of Infants in Infant Cardiopulmonary Resuscitation (CPR)
Training Mothers of Infants in Infant Cardiopulmonary Resuscitation (CPR) Using a 22-Minute Instructional DVD and Infant Manikin
This research will be a prospective, cohort study to determine if mothers of infants/newborns are more willing to complete CPR training using a 22-minute instructional DVD and infant manikin versus traditional four hour didactic instruction.
Study Hypothesis: A 22-minute instructional DVD and infant manikin will be an effective and preferred tool for teaching mothers of infants infant CPR.
Objectives
- To determine if mothers of infants are more likely to complete infant CPR training with a 22-minute instructional DVD and infant manikin, than by attending a traditional CPR class.
- To determine if learning infant CPR with a 22-minute instructional DVD and infant manikin is as effective as attending traditional infant CPR class.
- To examine the number of mothers that were offered the opportunity to learn infant CPR either as part of their prenatal classes, or upon the birth of their infant.
- To examine the number of mothers who have been previously trained in CPR.
- To examine the reasons that mothers have been previously trained in CPR (e.g., mandated by work/career vs. personal reasons).
- To examine the multiplier effect of an at home CPR education using a 22-minute instructional DVD and infant manikin at the time of the follow up phone call.
Study Overview
Detailed Description
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
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Pennsylvania
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Allentown, Pennsylvania, United States, 18103
- LeHigh Valley Hospital
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- Mother must be admitted to MBU at the CC site within twenty-four hours of giving birth.
- Mother must be eighteen years-old or greater.
Exclusion Criteria:
- Mother is not admitted to the MBU.
- Mother is under eighteen years-old.
- Mother has been inpatient for over twenty-four hours.
- Mother is physically incapable of performing CPR.
- Mother is cognitively impaired.
- Mother is unable to understand and sign consent.
- Mother is non-English speaking.
- Current pregnancy resulted in fetal demise.
- Mother who has previously participated in the study.
- Mother who has previously self-educated themselves in infant CPR using a 22-minute DVD and an infant manikin.
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Prevention
- Allocation: Non-Randomized
- Interventional Model: Single Group Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Active Comparator: CPR Class
mothers who are currently certified in CPR (i.e., have taken the traditional CPR class, or have been recertified in CPR by classroom instruction, within the past two years).
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These participants will be consented, surveyed, asked to watch a 22-minute instructional Infant CPR DVD with an infant manikin.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
---|---|
Participants will be given written and practical exams to assess their learned CPR skills
Time Frame: 6 months
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6 months
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Secondary Outcome Measures
Outcome Measure |
Time Frame |
---|---|
CPR learning experiences (e.g., ease, quality of instruction, convenience, ) will be analyzed from survey results
Time Frame: 6 months
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6 months
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Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Marna R Greenberg, D.O., MPH, LVH
Study record dates
Study Major Dates
Study Start
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Estimate)
Study Record Updates
Last Update Posted (Estimate)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- 2-20070911
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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