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Examining the Effects of an Improvisation Group

Examining the Effects of an Improvisation Group on Social Anxiety Among Help-seeking Youth

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03147924
Enrollment
5
Registered
2017-05-10
Start date
2017-03-06
Completion date
2017-08-31
Last updated
2018-04-30

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Anxiety, Depression, Self Concept Alteration, Social Support

Brief summary

This study is taking place to examine the preliminary effects of improvisational therapy (improv group) on social anxiety for youth at the Youth Wellness Centre (YWC). The improv group will run for 12-weeks as a drop-in group. A typical session will begin with stretching, simple breathing and an activity to promote group cohesion. Following this, improvisation games and activities will be introduced with the goal of promoting the following skills: assertiveness, acceptance, problem solving, co-operate skills, non-verbal communication, mindfulness, and memory. Youth who consent to the study will be asked to complete a set of brief questionnaires the first time they attend one of the sessions. Youth who have attended at least 3 sessions will be asked again to complete questionnaires following the completion of week 12 session. Youth will also rate their anxiety and distress on a simple rating scale at the beginning and end of each session. Additionally, all participants (who have attended three or more sessions) will be invited to complete a 30 to 45 minute qualitative interview following the 12 week session. Participants are predicted to show a decrease in social anxiety, generalized anxiety and depression symptoms, and an increase in self-esteem, and perceived social support.

Interventions

OTHERImprovisation Group

The aim of this pilot study is to investigate the effects of improvisational comedy in a group of help-seeking youth at risk of developing a range of mental health disorders, including social anxiety.

Sponsors

St. Joseph's Healthcare Hamilton
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
OTHER
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
17 Years to 25 Years
Healthy volunteers
Yes

Inclusion criteria

* help-seeking youth * ages 17-25

Exclusion criteria

* will NOT be excluded on the basis of mental health or addiction concerns

Design outcomes

Primary

MeasureTime frameDescription
Change in Generalized Anxiety Disorder 7 (GAD-7)Pre-group and 12-weeks later (post group)A seven-item self-report anxiety questionnaire designed to monitor and assess the severity of generalized anxiety disorder (GAD) symptoms.
Change in Social Phobia Inventory (SPIN)Pre-group and 12-weeks later (post group)A seventeen-item questionnaire used to measure the severity of social anxiety.
Change in Subjective Units of Distress Scale (SUDS)Pre and post every improv session for a duration of 12-weeksA thermometer scale used to track anxiety before and after each session

Secondary

MeasureTime frameDescription
Change in Patient Health Questionnaire (PHQ-9)Pre-group and 12-weeks later (post group)A nine-item questionnaire used to measure depression
Change in Multidimensional Scale of Perceived Social Support (MSPSS)Pre-group and 12-weeks later (post group)A 12-item questionnaire designed to measure perception of support from 3 sources: family, friends and significant other
Change in Kessler Psychological Distress Scale (K-10)Pre-group and 12-weeks later (post group)A 10-item questionnaire intended to measure distress based on questions about anxiety and depressive symptoms.
Change in Rosenberg Self-Esteem Scale (RSES)Pre-group and 12-weeks later (post group)A 10-item questionnaire used to measure self-esteem.

Countries

Canada

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026