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

H

Hebrew University of Jerusalem

Status

Enrolling

Conditions

Social Anxiety

Treatments

Behavioral: Imagery rescriptinf one-session
Behavioral: Imaginal exposure one-session

Study type

Interventional

Funder types

Other

Identifiers

NCT04635904
isf2157/2020

Details and patient eligibility

About

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.

Full 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.

Enrollment

100 estimated patients

Sex

All

Ages

18 to 70 years old

Volunteers

Accepts Healthy Volunteers

Inclusion and exclusion criteria

Inclusion Criteria: SPIN scores >= 30 -

Exclusion Criteria:

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

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

100 participants in 2 patient groups

Imaginal exposure
Experimental group
Description:
A behavioral intervention in imagery
Treatment:
Behavioral: Imaginal exposure one-session
Imagery rescripting
Experimental group
Description:
A different behavioral intervention in imagery
Treatment:
Behavioral: Imagery rescriptinf one-session

Trial contacts and locations

1

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Central trial contact

Jonathan D Huppert, PhD; Snir Barzilay, Grad student

Data sourced from clinicaltrials.gov

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