The Effect of a Non-Operating Room Anesthesia (NORA) Safety Video on Clinician Anxiety and Perceived Self-Efficacy

July 21, 2022 updated by: Louise Y. Wen, Dartmouth-Hitchcock Medical Center
The purpose of this study is to assess the effect of a non-operating room anesthesia (NORA) safety video on clinician anxiety and perceived self-efficacy.

Study Overview

Status

Completed

Conditions

Intervention / Treatment

Detailed Description

50 anesthesia professionals will be recruited from the Center for Surgical Innovation (CSI) non-operating room anesthesia (NORA) workforce. Participants will be asked to: Complete a five-minute pre-survey, watch a five-minute video, and then complete a five-minute post-survey.

Study Type

Interventional

Enrollment (Actual)

78

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

  • United States
    • New Hampshire
      • Lebanon, New Hampshire, United States, 03756
        • Dartmouth Hitchcock Medical Center

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

  • ADULT
  • OLDER_ADULT
  • CHILD

Accepts Healthy Volunteers

Yes

Genders Eligible for Study

All

Description

Inclusion Criteria:

  • Individuals employed at Dartmouth-Hitchcock Medical Center (DHMC) in the Department of Anesthesia who are eligible to work in the Center for Surgical Innovation (CSI).

Exclusion Criteria:

  • Individuals who are not employed at Dartmouth-Hitchcock Medical Center (DHMC) in the Department of Anesthesia and who are not eligible to work in the Center for Surgical Innovation (CSI).

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: HEALTH_SERVICES_RESEARCH
  • Allocation: NA
  • Interventional Model: SINGLE_GROUP
  • Masking: NONE

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
OTHER: Video
All participants are invited to complete a pre survey, watch a five minute video, and then complete a post survey.
Behavioral: Video
This 5-minute video presents clips with voiceover narration summarizing and highlighting the key safety points in the Center for Surgical Innovation (CSI) location.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Change in Anxiety
Time Frame: Before and after watching a five minute video, all occurring on the same day.
Anxiety levels about working in the Center for Surgical Innovation (CSI) will be measured via a series of questions developed by the study team. The survey consist of multiple questions and responses include a scale; The options include "Not at all", "A little", "Moderately", "Very much" and "Extremely".
Before and after watching a five minute video, all occurring on the same day.

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Change in Perceived self-efficacy
Time Frame: Before and after watching a five minute video, all occurring on the same day.
Perceived self-efficacy about working in the Center for Surgical Innovation (CSI) will be measured via a series of questions developed by the study team. The survey consist of multiple questions and responses include a scale; The options include "Not at all confident", "A little confident", "Moderately confident", "Very confident" and "Extremely confident".
Before and after watching a five minute video, all occurring on the same day.

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Sponsor

Dartmouth-Hitchcock Medical Center

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (ACTUAL)

December 1, 2021

Primary Completion (ACTUAL)

April 30, 2022

Study Completion (ACTUAL)

May 1, 2022

Study Registration Dates

First Submitted

January 6, 2022

First Submitted That Met QC Criteria

January 21, 2022

First Posted (ACTUAL)

February 2, 2022

Study Record Updates

Last Update Posted (ACTUAL)

July 25, 2022

Last Update Submitted That Met QC Criteria

July 21, 2022

Last Verified

July 1, 2022

More Information

Terms related to this study

Additional Relevant MeSH Terms

Other Study ID Numbers

  • STUDY02001332

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

IPD Plan Description

There are not plans to make individual participant data available at this time.

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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