Ultra-Brief Versus Brief Hands Only CPR Video Training With and Without Psychomotor Skill Practice
- Full Text View
- Tabular View
- Study Results
- Disclaimer
- How to Read a Study Record
Purpose
Bystander CPR improves survival from Out of Hospital Cardiac Arrest. This study examines the efficacy of ultra-brief video training for Hands-Only CPR. Subjects were randomized to one of four training conditions, then assessed for CPR skills retention.
| Condition | Intervention |
|---|---|
|
Cardiac Arrest |
Behavioral: No training, assessed within 60 mins Behavioral: Ultra-brief video; assessed in 60 mins Behavioral: Brief video; assessed in 60 mins Behavioral: Brief video + hands-on; ass'd in 60 mins Behavioral: Ultra-brief video; assessed at 2 months Behavioral: Brief video; assessed 2 months later Behavioral: Brief video + hands-on; ass'd 2 ms later |
| Study Type: | Interventional |
| Study Design: | Allocation: Randomized Endpoint Classification: Efficacy Study Intervention Model: Parallel Assignment Masking: Single Blind (Outcomes Assessor) Primary Purpose: Prevention |
| Official Title: | Comparison of the Effectiveness of Ultra-Brief and Brief Hands-Only CPR Video Training With and Without Psychomotor Skill Practice for Lay Responders: a Controlled Randomized Study |
- Median Compression Depth (mm) [ Time Frame: 60 minutes after intervention or two months after intervention ] [ Designated as safety issue: No ]Assessment of resuscitation skills using a Laerdal Resusci Annie recording manikin and Laerdal PC Skill Reporting software
- The Proportion of Subjects Who Assessed the Responsiveness of the Victim (Manikin) as Judged by Expert Raters [ Time Frame: 60 minutes after intervention and two months after intervention ] [ Designated as safety issue: No ]The proportion of the subjects who assessed the responsiveness of the victim (manikin) as judged by expert raters
| Enrollment: | 336 |
| Study Start Date: | September 2009 |
| Study Completion Date: | November 2009 |
| Primary Completion Date: | November 2009 (Final data collection date for primary outcome measure) |
| Arms | Assigned Interventions |
|---|---|
|
Experimental: No training, assessed within 60 mins
Subjects receive no training
|
Behavioral: No training, assessed within 60 mins
Subjects receive no training in resuscitation
Other Name: C-Group
|
|
Experimental: Ultra-brief video; assessed in 60 mins
Subjects receive an ultra-brief (90-second) video on hands-only CPR
|
Behavioral: Ultra-brief video; assessed in 60 mins
Subjects receive an ultra-brief (90-second) video on hands-only CPR
Other Name: UBV-Group
|
|
Experimental: Brief video; assessed in 60 mins
Subjects receive a brief (5-minute) video on hands-only CPR
|
Behavioral: Brief video; assessed in 60 mins
Subjects receive a brief (5-minute) video on hands-only CPR
Other Name: BV-Group
|
|
Experimental: Brief video + hands-on; ass'd in 60 mins
Subjects receive a brief (5-minute) video with hands-on manikin practice
|
Behavioral: Brief video + hands-on; ass'd in 60 mins
Subjects receive a brief (5-minute) video with hands-on manikin practice
Other Name: BVP-Group
|
| Experimental: Ultra-brief video; assessed at 2 months |
Behavioral: Ultra-brief video; assessed at 2 months
Subjects see ultra-brief video (90-seconds), are assessed two months later
Other Name: UBV-Group
|
| Experimental: Brief video; assessed 2 months later |
Behavioral: Brief video; assessed 2 months later
Subjects see brief video (5 minutes), are then assessed two months later
Other Name: BV-Group
|
| Experimental: Brief video + hands-on; ass'd 2 ms later |
Behavioral: Brief video + hands-on; ass'd 2 ms later
Subjects see brief (5-minute) video, receive hands-on training, and are assessed two months later
Other Name: BVP-Group
|
Detailed Description:
Bystander CPR improves survival from Out of Hospital Cardiac Arrest. This study is the first of its kind to examine the efficacy of ultra-brief video training for Hands-Only CPR without the use of a manikin. The results will inform future efforts to mass train citizens in CPR. Subjects were randomized to one of four training conditions, then assessed for CPR skills retention. The four groups were 1) no training; 2) ultra-brief training video (90 seconds); 3) short training video (5 minutes) with no practice; and 4) short training video with hands-on practice. The subjects were then evaluated for CPR skills retention. One half of the subjects were evaluated on the training day, and the other half were evaluated two months later.
Eligibility| Ages Eligible for Study: | 18 Years and older |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | Yes |
Inclusion Criteria:
- Members of a local area church
Exclusion Criteria:
- Less than 18 years old
- formal CPR training or certification within last 2 years
- Lacks fluency in English
- Works as a health care provider
Contacts and Locations
More Information
No publications provided by Maricopa Integrated Health System
Additional publications automatically indexed to this study by ClinicalTrials.gov Identifier (NCT Number):
| Responsible Party: | Bentley J Bobrow, MD, FACEP, FAAEM, Maricopa Integrated Health System |
| ClinicalTrials.gov Identifier: | NCT01191736 History of Changes |
| Other Study ID Numbers: | 2009-070 |
| Study First Received: | August 27, 2010 |
| Results First Received: | September 17, 2010 |
| Last Updated: | March 2, 2011 |
| Health Authority: | United States: Institutional Review Board |
Keywords provided by Maricopa Integrated Health System:
|
hands only CPR resuscitation cardiac arrest Education of general public regarding resuscitation methods |
Additional relevant MeSH terms:
|
Heart Arrest Heart Diseases Cardiovascular Diseases |
ClinicalTrials.gov processed this record on May 23, 2013