Imagery Rescripting and Imaginal Exposure for Social Anxiety: Mechanisms and Outcomes in an Analog Sample

  • STATUS
    Recruiting
  • days left to enroll
    5
  • participants needed
    100
  • sponsor
    Hebrew University of Jerusalem
Updated on 24 March 2022
Accepts healthy volunteers

Summary

This study will recruit 100 participants who self-report high symptoms of social anxiety (Social phobia inventory >30). Participants will be randomly assigned to receive either one analog intervention of Imagery Rescripting (IR) or Imaginal Exposure. We will test the efficacy and mechanisms behind each interventions.

Description

After being informed about the study potential risks, all patients giving written informed consent will undergo screening to determine eligibility for study entry. They will be randomly assigned to two conditions (Imagery rescripting Vs. Imaginal exposure) at a 1:1 ratio. Participants will attend three ~1 hour online ZOOM sessions (pre-assessment and measurement, intervention, and post assessment and measurement).

Assessors will be blind to the treatment condition.

Details
Condition Social Anxiety
Treatment Imaginal exposure one-session, Imagery rescriptinf one-session
Clinical Study IdentifierNCT04635904
SponsorHebrew University of Jerusalem
Last Modified on24 March 2022

Eligibility

Yes No Not Sure

Inclusion Criteria

SPIN scores >= 30 -

Exclusion Criteria

can't report a negative imagery related to a future social scenario. Attending active
psychotherapy sessions
Clear my responses

How to participate?

Step 1 Connect with a study center
What happens next?
  • You can expect the study team to contact you via email or phone in the next few days.
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Additional screening procedures may be conducted by the study team before you can be confirmed eligible to participate.

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If you are confirmed eligible after full screening, you will be required to understand and sign the informed consent if you decide to enroll in the study. Once enrolled you may be asked to make scheduled visits over a period of time.

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Complete your scheduled study participation activities and then you are done. You may receive summary of study results if provided by the sponsor.

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