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CompletedNCT05220943Updated Jul 25, 2022

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

An interventional study of Video in Anxiety and Self Efficacy, sponsored by Dartmouth-Hitchcock Medical Center. Completed at 1 site in United States. Per ClinicalTrials.gov, last updated 2022-07-25.

Sponsored by Dartmouth-Hitchcock Medical Center · Not applicable, Interventional, and Health services research

Phase
Not applicable
Study type
Interventional
Enrollment
78
Allocation
Not applicable
Sex
All
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Study summary

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.

Read the 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.

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Conditions studied

  • Anxiety
  • Self Efficacy

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03

In context

Anxiety Disorders

5,063 studies on the registry are indexed under Anxiety Disorders; 1,408 are open to participants now.

This study's enrollment of 78 is close to the median of 80 across 4,339 interventional studies indexed under Anxiety Disorders.

Browse Anxiety Disorders studies →

Lead sponsor

Dartmouth-Hitchcock Medical Center is the lead sponsor of 486 studies on the registry; 69 are open to participants now.

Of its 31 completed or terminated interventional studies of FDA-regulated products, 21 (68%) have results posted.

Counted across the registry records on this site, refreshed daily.

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Who can participate

Ages eligible
Child (0–17), Adult (18–64), Older adult (65+)
Sexes eligible
All
Accepts healthy volunteers
Yes

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

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

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).
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Study design

Phase
Not applicable
Primary purpose
Health services research
Allocation
Not applicable
Intervention model
Single group
Masking
None (open label)
Enrollment
78 participants (actual)

Study arms

  • Other
    Video

    All participants are invited to complete a pre survey, watch a five minute video, and then complete a post survey.

    Behavioral: Video

Interventions

  • BehavioralVideo

    This 5-minute video presents clips with voiceover narration summarizing and highlighting the key safety points in the Center for Surgical Innovation (CSI) location.

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What researchers measure

Primary outcomes

  1. Change in Anxiety

    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".

    Time frame: Before and after watching a five minute video, all occurring on the same day.

Secondary outcomes

  1. Change in Perceived self-efficacy

    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".

    Time frame: Before and after watching a five minute video, all occurring on the same day.

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Study locations

1 site
  • Dartmouth Hitchcock Medical Center
    Lebanon, New Hampshire 03756, United States
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References and documents

Individual participant data

Plan to share: No — There are not plans to make individual participant data available at this time.

No publications or documents are linked to this record.

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Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jul 25, 2022, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT05220943
Responsible party
Louise Y. Wen (Principal Investigator, Staff Physician, Anesthesiology, Dartmouth-Hitchcock Medical Center) — Principal investigator
First posted
Feb 2, 2022
Start date
Dec 1, 2021
Primary completion
Apr 30, 2022
Completion
May 1, 2022
Last update
Jul 25, 2022

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Jul 2022. You cannot join it, but the record below documents what was studied.

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