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Assessment of NAPS Performance. (NAPSAT)

This study has been completed.
Sponsor:
ClinicalTrials.gov Identifier:
NCT01768143
First Posted: January 15, 2013
Last Update Posted: August 20, 2014
The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.
Information provided by (Responsible Party):
Copenhagen University Hospital at Herlev
  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 ]
    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

Information from the National Library of Medicine

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Ages Eligible for Study:   18 Years to 90 Years   (Adult, Senior)
Sexes Eligible for Study:   All
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
Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT01768143


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

Responsible Party: Copenhagen University Hospital at Herlev
ClinicalTrials.gov Identifier: NCT01768143     History of Changes
Other Study ID Numbers: SPAT-003
First Submitted: January 9, 2013
First Posted: January 15, 2013
Last Update Posted: August 20, 2014
Last Verified: September 2013

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

Additional relevant MeSH terms:
Propofol
Hypnotics and Sedatives
Central Nervous System Depressants
Physiological Effects of Drugs
Anesthetics, Intravenous
Anesthetics, General
Anesthetics