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Body Dysmorphic Disorder clinical trials

View clinical trials related to Body Dysmorphic Disorder.

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NCT ID: NCT05402475 Recruiting - Clinical trials for Body Dysmorphic Disorder

Online Cognitive Behavioural Therapy Intervention for Body Dysmorphic Disorder

Start date: September 1, 2022
Phase: N/A
Study type: Interventional

Body Dysmorphic Disorder (BDD) affects 2.3% of the population and is characterized by excessive concerns with imagined or minor defects in physical appearance. Retrospective outcome studies suggest patients affected by BDD don't typically benefit from surgical treatments while cognitive behaviour therapy (CBT) appears to provide symptom - reducing and distress - reducing benefits. Two different 8-week online CBT approaches to assisting individuals with this disorder are compared: one approach will integrate mindfulness meditation methods (in combination with CBT) and one approach will employ CBT methods without reference to mindfulness meditation.

NCT ID: NCT04373629 Recruiting - Clinical trials for Body Dysmorphic Disorder

Perceptual Abnormalities and Their Malleability in BDD

Start date: December 1, 2020
Phase: N/A
Study type: Interventional

A core symptom of body dysmorphic disorder (BDD) is perceptual distortions for appearance, which contributes to poor insight and delusionality, limits engagement in treatment, and puts individuals at risk for relapse. Results from this study will provide a comprehensive mechanistic model of brain, behavioral, and emotional contributors to abnormal perceptual processing, as well as how malleable it is with visual modulation techniques. This will lay the groundwork for next-step translational perceptual retraining approaches.

NCT ID: NCT03673046 Completed - Clinical trials for Body Dysmorphic Disorder

Waitlist-Control Trial of Smartphone Cognitive Behavioral Therapy (CBT) for Body Dysmorphic Disorder (BDD)

Start date: September 17, 2019
Phase: N/A
Study type: Interventional

The investigators are testing the efficacy of Smartphone-delivered cognitive behavioral therapy (CBT) treatment for body dysmorphic disorder (BDD). The investigators hypothesize that participants receiving app-CBT will have greater improvement in body dysmorphic disorder symptom severity than those in the waitlist condition at treatment endpoint (week 12).

NCT ID: NCT02843451 Withdrawn - Clinical trials for Body Dysmorphic Disorder

Milk Thistle in Body Dysmorphic Disorder

Start date: October 2016
Phase: Phase 2
Study type: Interventional

The proposed study will consist of a 9 week double-blind cross-over study trial of milk thistle in 15 people (ages 18-65). The study will be divided into an initial 4 week phase, a one week wash out phase, and a second 4 week phase, with one of the 4 week phases consisting of active treatment with milk thistle, and the other 4 week phase consisting of inactive placebo treatment. Participants will be randomized to receive either milk thistle or placebo during the first 4 week phase on a 1:1 basis. This blinding will be maintained by the IDS pharmacy at the University of Chicago.

NCT ID: NCT02808702 Completed - Social Phobia Clinical Trials

Brain Correlates of Self-Focused Processing

Start date: May 1, 2017
Phase: N/A
Study type: Interventional

The purpose of this study is to determine whether neuroimaging-based markers of maladaptive self-focused processing are better predictors of treatment response to cognitive-behavioral therapy than behavioral markers.

NCT ID: NCT02671266 Completed - Clinical trials for Obsessive-compulsive Disorder

Oxytocin Administration in BDD and OCD

Start date: December 2014
Phase: Phase 2
Study type: Interventional

The purpose of the current study is to investigate the effect of an acute administration of intranasal oxytocin, relative to placebo, on social cognitive impairments among individuals with body dysmorphic disorder and obsessive-compulsive disorder, compared to healthy controls.

NCT ID: NCT02635152 Completed - Clinical trials for Body Dysmorphic Disorder

Interpretation Bias Modification for Body Dysmorphic Disorder

Start date: September 2015
Phase: N/A
Study type: Interventional

The purpose of this study is to determine whether a computerized intervention designed to reduce appearance and evaluation related interpretation biases will reduce symptoms associated with body dysmorphic disorder.

NCT ID: NCT02010619 Completed - Clinical trials for Body Dysmorphic Disorder

Internet Delivered CBT for Body Dysmorphic Disorder

Start date: November 2013
Phase: N/A
Study type: Interventional

To evaluate if Internet delivered cognitive behavior therapy is an efficacious treatment when compared to a control group consisting of supportive therapy.

NCT ID: NCT01453439 Completed - Anxiety Disorders Clinical Trials

Cognitive-Behavioral Therapy and Supportive Psychotherapy for Body Dysmorphic Disorder

Start date: August 2011
Phase: N/A
Study type: Interventional

The purpose of this study is to learn more about two different types of psychotherapy to help individuals who have body dysmorphic disorder (BDD). BDD is a severe, often chronic, and common disorder consisting of distressing or impairing preoccupation with perceived defects in one's physical appearance. Individuals with BDD have very poor psychosocial functioning and high rates of hospitalization and suicidality. Because BDD differs in important ways from other disorders, psychotherapies for other disorders are not adequate for BDD. Despite BDD's severity, there is no adequately tested psychosocial treatment (psychotherapy) of any type for this disorder. This study will compare the effectiveness of Cognitive Behavioral Therapy and Supportive Psychotherapy as well as predictors of improvement.

NCT ID: NCT01398865 Completed - Clinical trials for Body Dysmorphic Disorder

Escitalopram Neuroimaging Supplement

Start date: December 2008
Phase: N/A
Study type: Observational

The purpose of this study is to find out more about the brain's response to selective serotonin reuptake inhibitor (SSRIs) treatment in people with body dysmorphic disorder (BDD). The investigators will use positron emission tomography (PET) and Magnetic Resonance Imaging (MRI) scans to look at brain activity in people with BDD before and after treatment with an SSRI. The investigators hope that what is learned will allow prediction of whether someone will improve with SSRI treatment.