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NCT Number: NCT07355998

Medical Improvisation Study

This study offers improvisation training for otolaryngology residents to see if there is any impact on connection, stress, and mood. A control group of otolaryngology residents continues their standard medical education with no improvisation.

Active, Not Recruiting

This study is active but is not currently recruiting participants.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

UCSF

San Francisco, California, 94143, United States

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Otolaryngology Resident at UCSF

Treatment and study plan

Group Online Improvisation Training

Behavioral

3 Online Group Improvisation Training classes led by a professional is offered every other week for 1 hour to the experimental cohort.

standard medical education

Other

OHNS residents continue the existing standard medical education.

Primary outcomes

  1. Connection: Social Connectiveness Scale

    Time frame: 6 weeks

    Team dynamics and interpersonal connectedness are assessed using the Social Connectedness Scale. This is a custom survey developed specifically for this study to measure participants' sense of belonging and connection within the residency program. The scale consists of 5 items rated on a 5-point Likert scale. Total scores range from 0 to 25, with higher scores indicating a greater sense of connectedness (better outcome).

  2. Clinical Decision Making Accuracy and Response Time

    Time frame: 6 weeks

    Clinical decision-making under pressure is assessed using the "Intraoperative Vignettes" assessment. This is a computer-based cognitive test comprising 20 Otolaryngology-Head and Neck Surgery (OHNS) case scenarios. Participants are presented with clinical scenarios and must select the correct management decision. The outcome is reported as a composite of accuracy (total number of correct responses) and response time (time taken to select an answer). Accuracy is scored from 0 to 20, with higher scores indicating better clinical decision-making.

Secondary outcomes

  1. Mood (PANAS)

    Time frame: 6 weeks

    Mood is assessed using the Positive and Negative Affect Schedule (PANAS). This is a validated 20-item self-report questionnaire that measures two distinct dimensions of emotion: Positive Affect (10 items) and Negative Affect (10 items). Participants rate items on a 5-point scale ranging from 1 (Very slightly or not at all) to 5 (Extremely). Scores for each subscale range from 10 to 50.

    • Positive Affect: Higher scores represent higher levels of enthusiasm and energy (better outcome).
    • Negative Affect: Higher scores represent higher levels of subjective distress and unpleasurable engagement (worse outcome).
  2. Anxiety and Depression (DASS-21)

    Time frame: 6 weeks

    Psychological distress is measured using the Depression, Anxiety, and Stress Scale-21 (DASS-21). This is a validated 21-item self-report instrument containing three subscales: Depression, Anxiety, and Stress (7 items per subscale). Participants rate how much each statement applied to them over the past week on a 4-point scale ranging from 0 (Did not apply to me at all) to 3 (Applied to me very much or most of the time). Subscale scores are calculated by summing the scores for the relevant items and multiplying by 2.

    • Range: Each subscale ranges from 0 to 42.
    • Interpretation: Higher scores indicate greater severity of symptoms (worse outcome).
  3. Intervention Satisfaction Score (Intervention Arm Only)

    Time frame: 6 weeks

    Participants in the intervention group complete an Intervention Satisfaction Survey to evaluate the curriculum and learner experience. This measure utilizes a Likert scale to assess participant feedback. Items are rated on a 5-point scale from 1 (Not true at all) to 5 (Completely true), with higher scores indicating higher satisfaction (better outcome).

Sponsors and collaborators

Lead sponsor

University of California, San Francisco

Other

Registry information

Official study title

Enhancing Communication and Cognitive Resilience in Surgical Trainees Through Medical Improvisation

Important dates

Study start
2025
Primary completion
2026
Study completion
2026
First posted
Jan 21, 2026
Registry last updated
Feb 5, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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