Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
NCT06346301

Imagery Rescripting as a Stand-alone Treatment for OCD and BDD.

Led by Academisch Medisch Centrum - Universiteit van Amsterdam (AMC-UvA) · Updated on 2024-04-04

36

Participants Needed

1

Research Sites

193 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

The goal of this multiple baseline case series study is to test the effect of imagery rescripting (ImRs) in Obsessive Compulsive Disorder (OCD) and Body Dysmorphic Disorder (BDD). Primary objective :The course of schema or core beliefs and change in OCD and BDD. To investigate the effectiveness of imagery rescripting on factors presumed to underlie the disorder, according to schema theory, and on OCD and BDD symptoms. Secondary objective: The change in OCD and BDD symptoms (full questionnaire), schemata and modes, core emotions, mood, affect and obtrusiveness of intrusion. Other objectives are research into the working mechanisms of imagery rescripting by collecting qualitative data from patients and their practitioner in a qualitative interview. For this study, a multiple-baseline single-case experimental design (SCED) is used testing different outcome variables in 18 OCD patients and 18 BDD patients. After a variable baseline period of 3-8 weeks participants will start twice weekly with imagery rescripting for 12 sessions, followed by a 6 week follow up. Participants will rate schema- or core beliefs and OCD or BDD severity on a visual analogue scale. In addition participants will rate core emotions, affect and obtrusiveness of the intrusion. Secondary we will asses four times questionnaires about OCD of BDD symptoms, depression and schemas en modes. After treatment participants will be interviewed about their experiences.

CONDITIONS

Official Title

Imagery Rescripting as a Stand-alone Treatment for OCD and BDD.

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Meet the criteria for OCD or BDD as a primary diagnosis according to DSM-5
  • Are aged 18 years or older
  • Can read and write Dutch
  • Have a Yale Brown Obsessive Compulsive Scale (Y-BOCS) score of 20 or higher
  • Have had a stable dose of medication for at least 6 weeks before the study
Not Eligible

You will not qualify if you...

  • Current manic or hypomanic episode
  • Active suicidal plans
  • Current psychosis (except for delusions related to the disorder)
  • Diagnosed alcohol or drug abuse
  • Electroconvulsive therapy within the last 6 months
  • Neurological disorder or an Intelligence Quotient (IQ) below 80

AI-Screening

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Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Department of Psychiatry, AMC

Amsterdam-Zuidoost, North Holland, Netherlands, 1105 AZ

Actively Recruiting

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Research Team

T

Tibor van Verseveld

CONTACT

J

Judy Luigjes

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NA

Model

SINGLE_GROUP

Primary Purpose

TREATMENT

Number of Arms

1

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