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Completed

NCT Number: NCT01191736

Ultra-Brief Versus Brief Hands Only CPR Video Training With and Without Psychomotor Skill Practice

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.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

About this study

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.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

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

Treatment and study plan

No training, assessed within 60 mins

Behavioral

Subjects receive no training in resuscitation

Other names: C-Group

Ultra-brief video; assessed in 60 mins

Behavioral

Subjects receive an ultra-brief (90-second) video on hands-only CPR

Other names: UBV-Group

Brief video; assessed in 60 mins

Behavioral

Subjects receive a brief (5-minute) video on hands-only CPR

Other names: BV-Group

Brief video + hands-on; ass'd in 60 mins

Behavioral

Subjects receive a brief (5-minute) video with hands-on manikin practice

Other names: BVP-Group

Ultra-brief video; assessed at 2 months

Behavioral

Subjects see ultra-brief video (90-seconds), are assessed two months later

Other names: UBV-Group

Brief video; assessed 2 months later

Behavioral

Subjects see brief video (5 minutes), are then assessed two months later

Other names: BV-Group

Brief video + hands-on; ass'd 2 ms later

Behavioral

Subjects see brief (5-minute) video, receive hands-on training, and are assessed two months later

Other names: BVP-Group

Primary outcomes

  1. Median Compression Depth (mm)

    Time frame: 60 minutes after intervention or two months after intervention

    Assessment of resuscitation skills using a Laerdal Resusci Annie recording manikin and Laerdal PC Skill Reporting software

Secondary outcomes

  1. 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

    The proportion of the subjects who assessed the responsiveness of the victim (manikin) as judged by expert raters

Sponsors and collaborators

Lead sponsor

Valleywise Health

Other

Collaborators

  • American Heart Association
  • University of Arizona

Registry information

Official study 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

Important dates

Study start
2009
Primary completion
2009
Study completion
2009
First posted
Aug 31, 2010
Registry last updated
Mar 7, 2011

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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