Assessment of NAPS Performance. (NAPSAT)

This study has been completed.
Sponsor:
Information provided by (Responsible Party):
Copenhagen University Hospital at Herlev
ClinicalTrials.gov Identifier:
NCT01768143
First received: January 9, 2013
Last updated: August 19, 2014
Last verified: September 2013
  Purpose

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.


Condition Intervention
Competence in Propofol Sedation for Endoscopy
Behavioral: unexperienced endoscopy nurses
Behavioral: Experienced endoscopy nurses

Study Type: Observational
Study Design: Observational Model: Cohort
Time Perspective: Prospective
Official Title: A Reliable and Valid Assessment of Nurse Administered Propofol Sedation (NAPS) Performance.

Resource links provided by NLM:


Further study details as provided by Copenhagen University Hospital at Herlev:

Primary Outcome Measures:
  • Assessed sedation performance score [ Time Frame: 6 months ] [ Designated as safety issue: No ]
    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.


Enrollment: 12
Study Start Date: January 2013
Study Completion Date: June 2013
Primary Completion Date: March 2013 (Final data collection date for primary outcome measure)
Groups/Cohorts Assigned Interventions
Nurse Trainees
unexperienced endoscopy nurses
Behavioral: unexperienced endoscopy nurses
Nurse Experts
Educated endoscopy Nurses
Behavioral: Experienced endoscopy nurses

  Eligibility

Ages Eligible for Study:   18 Years to 90 Years
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   Yes
Sampling Method:   Probability Sample
Study Population

Endoscopy nurses of different competencylevel

Criteria

Inclusion Criteria:

  • eligible nurses, written informed consent.

Exclusion Criteria:

  • Prior anesthesia or ICU experience
  Contacts and Locations
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Please refer to this study by its ClinicalTrials.gov identifier: NCT01768143

Locations
Denmark
Herlev Hospital, Gastroenheden
Copenhagen, Herlev, Herlev, Denmark, 2730
Sponsors and Collaborators
Copenhagen University Hospital at Herlev
  More Information

No publications provided

Responsible Party: Copenhagen University Hospital at Herlev
ClinicalTrials.gov Identifier: NCT01768143     History of Changes
Other Study ID Numbers: SPAT-003
Study First Received: January 9, 2013
Last Updated: August 19, 2014
Health Authority: Denmark: Dataprotection Agency

Keywords provided by Copenhagen University Hospital at Herlev:
Propofol
Sedation
Endoscopy
nonanesthesiologist

ClinicalTrials.gov processed this record on October 21, 2014