Medical Improvisation Study
Enhancing Communication and Cognitive Resilience in Surgical Trainees Through Medical Improvisation
1 other identifier
interventional
10
1 country
1
Brief Summary
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.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at below P25 for not_applicable
Started Nov 2025
Shorter than P25 for not_applicable
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
November 15, 2025
CompletedFirst Submitted
Initial submission to the registry
January 2, 2026
CompletedFirst Posted
Study publicly available on registry
January 21, 2026
CompletedPrimary Completion
Last participant's last visit for primary outcome
February 1, 2026
CompletedStudy Completion
Last participant's last visit for all outcomes
February 1, 2026
CompletedFebruary 5, 2026
February 1, 2026
3 months
January 2, 2026
February 2, 2026
Conditions
Outcome Measures
Primary Outcomes (2)
Connection: Social Connectiveness Scale
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).
6 weeks
Clinical Decision Making Accuracy and Response Time
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.
6 weeks
Secondary Outcomes (3)
Mood (PANAS)
6 weeks
Anxiety and Depression (DASS-21)
6 weeks
Intervention Satisfaction Score (Intervention Arm Only)
6 weeks
Study Arms (2)
Improvisation Group
EXPERIMENTALOtolaryngology Residents taking Improvisation Training
Control Group
ACTIVE COMPARATORThis control group of OHNS residents continues their standard medical education.
Interventions
3 Online Group Improvisation Training classes led by a professional is offered every other week for 1 hour to the experimental cohort.
OHNS residents continue the existing standard medical education.
Eligibility Criteria
You may qualify if:
- Otolaryngology Resident at UCSF
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
UCSF
San Francisco, California, 94143, United States
Study Officials
- PRINCIPAL INVESTIGATOR
Karen Barrett, PhD
University of California, San Francisco
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- NON RANDOMIZED
- Masking
- NONE
- Purpose
- SUPPORTIVE CARE
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
January 2, 2026
First Posted
January 21, 2026
Study Start
November 15, 2025
Primary Completion
February 1, 2026
Study Completion
February 1, 2026
Last Updated
February 5, 2026
Record last verified: 2026-02
Data Sharing
- IPD Sharing
- Will not share