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Improvisation Workshops for Imposter Syndrome
N/A
Waitlist Available
Led By Esther Bui, MD
Research Sponsored by University Health Network, Toronto
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 3 months
Awards & highlights
No Placebo-Only Group
Summary
This trial explores whether improvisation workshops can help medical trainees at the University of Toronto feel more confident and less doubtful about their abilities. The workshops involve spontaneous activities that encourage quick thinking in a supportive setting.
Who is the study for?
This trial is for full-time medical trainees at the University of Toronto who feel like impostors despite evidence of their competence. It's not open to those involved in similar improv studies or activities, or part-time students.
What is being tested?
The study tests if improvisation workshops throughout an academic year can help reduce feelings associated with imposter syndrome among medical trainees, using a scale called CIPS to measure changes.
What are the potential side effects?
Since this intervention involves participation in workshops rather than medication, typical drug side effects are not expected. Participants may experience discomfort or anxiety during social and performance-based activities.
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ 3 months
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~3 months
Treatment Details
Study Objectives
Study objectives can provide a clearer picture of what you can expect from a treatment.Primary study objectives
Impostor phenomenon score
Secondary study objectives
Burnout
Perceived stress score
Resilience score
Awards & Highlights
No Placebo-Only Group
All patients enrolled in this study will receive some form of active treatment.
Trial Design
2Treatment groups
Experimental Treatment
Active Control
Group I: Improvisation WorkshopsExperimental Treatment1 Intervention
Participants will take part in an improvisation curriculum containing a uniquely designed series of flexibly-timed improvisation workshops administered during the study period. Using published guidelines, workshops will have groups of approximately 10 study participants and last on average 2 hours under the instruction of an expert medical improvisation facilitator.
Group II: ObservationalActive Control1 Intervention
Treatment
First Studied
Drug Approval Stage
How many patients have taken this drug
Improvisation Workshop
2022
N/A
~200
Research Highlights
Information in this section is not a recommendation. We encourage patients to speak with their healthcare team when evaluating any treatment decision.Mechanism Of Action
Side Effect Profile
Prior Approvals
Other Research
Common treatments for Imposter Syndrome, such as improvisation workshops and cognitive-behavioral therapy (CBT), work by enhancing self-confidence and reducing self-doubt. Improvisation workshops provide a safe space for individuals to practice spontaneous thinking and public speaking, which helps reduce anxiety and build self-efficacy.
CBT helps patients identify and challenge negative thought patterns, replacing them with more realistic and positive beliefs about their abilities. These interventions are crucial for Imposter Syndrome patients as they address the core issues of fraudulence and self-doubt, leading to improved mental health and career satisfaction.
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Who is running the clinical trial?
University of TorontoOTHER
719 Previous Clinical Trials
1,042,352 Total Patients Enrolled
University Health Network, TorontoLead Sponsor
1,524 Previous Clinical Trials
503,004 Total Patients Enrolled
Postgraduate Medical Education, University of TorontoUNKNOWN
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Eligibility Criteria:
This trial includes the following eligibility criteria:- You are a student of the University of Toronto.\n
Research Study Groups:
This trial has the following groups:- Group 1: Observational
- Group 2: Improvisation Workshops
Awards:
This trial has 1 awards, including:- No Placebo-Only Group - All patients enrolled in this study will receive some form of active treatment.
Timeline:
This trial has the following timeline:- Screening: It may take up to 3 Weeks to process to see if you qualify in this trial.
- Treatment: The duration you will receive the treatment varies.
- Follow Ups: You may be asked to continue sharing information regarding the trial for 6 Months after you stop receiving the treatment.
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