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Clinical Trials/NCT01768143
NCT01768143CompletedNot Applicable

A Reliable and Valid Assessment of Nurse Administered Propofol Sedation (NAPS) Performance.

Copenhagen University Hospital at Herlev1 site in 1 country12 target enrollmentStarted: January 2013Last updated:
Conditions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Sponsor
Enrollment
12
Locations
1
Primary Endpoint
Assessed sedation performance score

Study Overview

Brief Summary

To measure competencies in propofol sedation for endoscopic procedures (NAPS)through development, test and validation of a reliable assessment tool in a simulator setting.

Hypothesis: That the tool will demonstrate content and construct validity, ie. enable reliable measuring of necessary competencies of different levels in a reproducible way.

Study Design

Study Type
Observational
Observational Model
Cohort
Time Perspective
Prospective

Eligibility Criteria

Ages
18 Years to 90 Years (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
Yes

Inclusion Criteria

  • eligible nurses, written informed consent.

Exclusion Criteria

  • Prior anesthesia or ICU experience

Outcomes

Primary Outcomes

Assessed sedation performance score

Time Frame: 6 months

A Total of 12 Global Rating Scores and 2 checklist scores on hands on performance in a simulation setting and a theoretical Multiple Choice questionnaire. The performance score is decided by independent raters who review performances on video.

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor
Copenhagen University Hospital at Herlev
Sponsor Class
Other
Responsible Party
Sponsor

Study Sites (1)

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