NCT06673407

Brief Summary

The purpose of the study is to investigate the effects of four versions of a workshop for social anxiety and public speaking stress. All participants are current University of Colorado Boulder undergraduate students. Participation in this research study lasts for approximately 8 weeks, and includes a pre-workshop questionnaire, 3 weekly workshop sessions (ranging from 2 to 3 hours each, including a 5-minute post-session questionnaire), a post-workshop questionnaire, and a 1-month follow-up questionnaire.

Trial Health

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Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Trial has exceeded expected completion date
Enrollment
200

participants targeted

Target at P75+ for not_applicable

Timeline
Completed

Started Jun 2024

Geographic Reach
1 country

1 active site

Status
recruiting

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

June 12, 2024

Completed
4 months until next milestone

First Submitted

Initial submission to the registry

October 8, 2024

Completed
27 days until next milestone

First Posted

Study publicly available on registry

November 4, 2024

Completed
11 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

October 1, 2025

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

October 1, 2025

Completed
Last Updated

May 20, 2025

Status Verified

May 1, 2025

Enrollment Period

1.3 years

First QC Date

October 8, 2024

Last Update Submit

May 15, 2025

Conditions

Keywords

Social AnxietyPublic Speaking AnxietyExposure TherapyPeer-ledSelf-compassionCommon Humanity

Outcome Measures

Primary Outcomes (6)

  • Attendance rate

    Average number of workshop sessions attended by enrolled research participants.

    3 weeks during the intervention (workshops 1, 2, and 3, 1 week apart)

  • Enrollment rate

    Ratio of screened, eligible participants who enrolled in the study.

    Pre-intervention (from screening to enrollment)

  • Acceptability of Intervention Measure (AIM)

    Workshop satisfaction rating, Range = 1 - 5, Higher scores indicate better outcome (greater acceptability)

    48 hours after the final intervention session and 1-month follow-up

  • Client Satisfaction Questionnaire-8 (CSQ-8)

    Satisfaction with workshops, Range = 8 - 32, Higher scores indicate better outcome (greater satisfaction)

    48 hours after the final intervention session and 1-month follow-up

  • Social Phobia Inventory (SPIN)

    Social anxiety symptom measure, Range = 0 - 68, Higher scores indicate worse outcome (worse social phobia)

    48 hours after the final intervention session and 1-month follow-up

  • Liebowitz Social Anxiety Scale (LSAS)

    Measure assessing fear/anxiety across a broad range of social and performance situations, Range = 0 - 144, Higher scores indicate worse outcome (worse social anxiety)

    48 hours after the final intervention session and 1-month follow-up

Secondary Outcomes (13)

  • Personal Report of Communication Apprehension (PRCA-24)

    48 hours after the final intervention session and 1-month follow-up

  • Fidelity

    3 weeks during the intervention (workshops 1, 2, and 3, 1 week apart)

  • Contamination

    3 weeks during the intervention (workshops 1, 2, and 3, 1 week apart)

  • Study Burden

    48 hours after the final intervention session and 1-month follow-up

  • Survey Completion

    between 10 and 0 days before the first intervention session, 48 hours after the final intervention session, and 1-month follow-up

  • +8 more secondary outcomes

Study Arms (4)

Exposure Only

ACTIVE COMPARATOR

Group exposure therapy for social anxiety and public speaking fears.

Behavioral: Group Exposure for Social Anxiety

Compassion Enhanced

EXPERIMENTAL

Group exposure therapy for social anxiety and public speaking fears plus self-compassion exercises aimed at inducing a sense of common humanity.

Behavioral: Self-Compassion Enhanced Group Exposure Therapy for Social Anxiety

Peer enhanced

EXPERIMENTAL

Group exposure therapy for social anxiety and public speaking fears facilitated by a pair of doctoral student and undergraduate student co-facilitators who will explicitly use appropriate self-disclosure to establish the co-facilitators as individuals with lived experiences of social anxiety and public speaking fears.

Behavioral: Peer-Enhanced Group Exposure Therapy for Social Anxiety

Fully enhanced

EXPERIMENTAL

Group exposure therapy for social anxiety and public speaking fears plus self-compassion exercises aimed at inducing a sense of common humanity, facilitated by a pair of doctoral student and undergraduate student co-facilitators who will explicitly use appropriate self-disclosure to establish the co-facilitators as individuals with lived experiences of social anxiety and public speaking fears.

Behavioral: Peer and Self-Compassion Enhanced Group Exposure Therapy for Social Anxiety

Interventions

Group exposure therapy for social anxiety and public speaking fears.

Exposure Only

Group exposure therapy for social anxiety and public speaking fears plus piloted exercises from the investigators' previous studies among socially anxious undergraduates (Slivjak et al., 2022; Slivjak \& Arch, in preparation), refined during the investigators' quality improvement project, that are designed to enhance compassion.

Compassion Enhanced

Group exposure therapy for social anxiety and public speaking fears facilitated by a pair of doctoral student and undergraduate student co-facilitators who explicitly use appropriate self-disclosure to establish the co-facilitators as individuals with lived experiences of social anxiety and public speaking fears.

Peer enhanced

Group exposure therapy for social anxiety and public speaking fears plus piloted exercises from the investigators' previous studies among socially anxious undergraduates (Slivjak et al., 2022; Slivjak \& Arch, in preparation), refined during the investigators' quality improvement project, that are designed to enhance compassion. These groups are facilitated by a pair of doctoral student and undergraduate student co-facilitators who explicitly use appropriate self-disclosure to establish the co-facilitators as individuals with lived experiences of social anxiety and public speaking fears.

Fully enhanced

Eligibility Criteria

Age18 Years - 30 Years
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64)

You may qualify if:

  • Age = 18-30
  • Able to read and write fluently in English
  • Current undergraduate students at CU
  • Experiencing elevated social anxiety symptoms indicated by a SPIN score ≥ 19
  • Experiencing moderate to high communication anxiety indicated by a PRCA- 24 score ≥ 59
  • Open to receiving help for social anxiety or public speaking fears indicated by a help seeking score of ≥ 3 out of 5 (at both screening timepoints as explained below)
  • Able to voluntarily consent to participation
  • Able to participate fully in the study (including in the in-person group workshops and in survey completion) as assessed by screening questions and the study P

You may not qualify if:

  • Are currently experiencing moderately severe or severe depression represented by the validated cutoff score for major depression on the PHQ-8 of greater than 14 (Kroenke et al., 2001)
  • Score in the moderate-high range for suicide risk as indicated by the CSSRS (Salvi, 2019), report a suicide attempt in the past 12 months, or report current, ongoing suicidal ideation along with a past (lifetime) suicide attempt
  • Are current students of the PI or clients or current students of the doctoral student co-facilitators

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Renee Crown Wellness Institute and Department of Psychology & Neuroscience, University of Colorado Boulder

Boulder, Colorado, 80302, United States

RECRUITING

MeSH Terms

Conditions

Phobia, SocialGlossophobia

Condition Hierarchy (Ancestors)

Phobic DisordersAnxiety DisordersMental Disorders

Central Study Contacts

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
SINGLE
Who Masked
PARTICIPANT
Purpose
TREATMENT
Intervention Model
FACTORIAL
Model Details: This trial uses a 2-variable full factorial design within the Multiphase Optimization Strategy (MOST) framework. Participants will be assigned to one of four study conditions involving 5.5-7.5-hours of workshops (depending on study condition) conducted over 3 in-person group sessions. Study conditions will vary depending on whether they 1) include self-compassion (i.e., common humanity) enhancements, and 2) are led by peer co-facilitators.
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Yvonne Kristy Endowed Chair, Renée Crown Wellness Institute; Professor, Department of Psychology and Neuroscience

Study Record Dates

First Submitted

October 8, 2024

First Posted

November 4, 2024

Study Start

June 12, 2024

Primary Completion

October 1, 2025

Study Completion

October 1, 2025

Last Updated

May 20, 2025

Record last verified: 2025-05

Data Sharing

IPD Sharing
Will not share

Locations