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OpenTrials
Completed

NCT Number: NCT02059109

Evaluation of a Training Model for the Proficient Use of the Belmont Rapid Infuser

The Belmont Rapid Infuser is a device currently approved to replace larger volumes of necessary fluids such as blood in a fast and safe manner. The purpose of the study is to evaluate proficiency and the retention of knowledge of how to use the device based on current methods of training compared to revised training methods.

Hypotheses:

1. The use of the traditional method of training is not effective, predicting less then half of staff will pass on the first attempt. 2. Restructured test with hands-on training as opposed to oral presentation only with a written test will result in a pass rate of > 80%. 3. Staff members who work in pairs will perform better than working alone when setting up the Belmont Rapid Infuser (BRI). 4. Retention at 3 months will be higher with the restructured training method than with the traditional training method.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Cincinnati Children's Medical Center

Cincinnati, Ohio, 45229-3039, United States

About this study

Participants will be recruited to complete a test after undergoing either the traditional or the restructured training method. This training will be completed on one day and takes about 1 hour.

All participants who pass via either method of training are evaluated again to test retention 3-4 months later .

Who can participate

Healthy volunteers accepted: Yes

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

Inclusion criteria

  • Participants will be recruited from the faculty, Certified Registered Nurse Anesthetists, and fellows from the Department of Anesthesia at Cincinnati Children's Hospital Medical Center.
  • They may have had educational exposure or use of the Belmont Rapid Infuser without independent assembly.

Exclusion criteria

  • None

Treatment and study plan

Hands on Assembly of Belmont Rapid Infuser

Procedure

Participants will work individually or in pairs to assemble the Belmont Rapid Infuser in addition to completing the traditional training methods.

Primary outcomes

  1. Proficiency

    Time frame: Measured after the training session (approximately 1 hour).

    The composite score of "pass-pass" on BRI assembly and on knowledge test .

Secondary outcomes

  1. Retention of proficiency

    Time frame: 3 -4 months after delivery of the effective teaching model.

Sponsors and collaborators

Lead sponsor

Children's Hospital Medical Center, Cincinnati

Other

Registry information

Important dates

Study start
2013
Primary completion
2017
Study completion
2017
First posted
Feb 11, 2014
Registry last updated
Mar 21, 2018

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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