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Clinical Trials/NCT03147924
NCT03147924
Completed
Not Applicable

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

St. Joseph's Healthcare Hamilton1 site in 1 country5 target enrollmentMarch 6, 2017

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Anxiety
Sponsor
St. Joseph's Healthcare Hamilton
Enrollment
5
Locations
1
Primary Endpoint
Change in Generalized Anxiety Disorder 7 (GAD-7)
Status
Completed
Last Updated
8 years ago

Overview

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.

Registry
clinicaltrials.gov
Start Date
March 6, 2017
End Date
August 31, 2017
Last Updated
8 years ago
Study Type
Interventional
Study Design
Single Group
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Juliana Tobon

Psychologist

St. Joseph's Healthcare Hamilton

Eligibility Criteria

Inclusion Criteria

  • help-seeking youth
  • ages 17-25

Exclusion Criteria

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

Outcomes

Primary Outcomes

Change in Generalized Anxiety Disorder 7 (GAD-7)

Time Frame: 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)

Time Frame: 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)

Time Frame: Pre and post every improv session for a duration of 12-weeks

A thermometer scale used to track anxiety before and after each session

Secondary Outcomes

  • Change in Rosenberg Self-Esteem Scale (RSES)(Pre-group and 12-weeks later (post group))
  • Change in Multidimensional Scale of Perceived Social Support (MSPSS)(Pre-group and 12-weeks later (post group))
  • Change in Patient Health Questionnaire (PHQ-9)(Pre-group and 12-weeks later (post group))
  • Change in Kessler Psychological Distress Scale (K-10)(Pre-group and 12-weeks later (post group))

Study Sites (1)

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