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Obsessive-Compulsive Disorder clinical trials

View clinical trials related to Obsessive-Compulsive Disorder.

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NCT ID: NCT05240924 Recruiting - Clinical trials for Obsessive Compulsive Disorder (OCD)

ERP to Improve Functioning in Veterans With OCD

Start date: October 3, 2022
Phase: N/A
Study type: Interventional

Obsessive compulsive disorder (OCD) is a debilitating psychiatric illness impacting work, social, and family functioning. Exposure and Response Prevention (ERP) is the sole evidence-based psychotherapy for OCD; however, no randomized controlled trials (RCTs) have examined the effectiveness of ERP among Veterans or individuals with both OCD and posttraumatic stress disorder (PTSD). This 4-year Hybrid Type I trial will compare outcomes of ERP to those of a control condition among Veterans with OCD. Primary and secondary aims will examine whether Veterans' functioning, quality of life, and OCD symptoms differ between the ERP and control in the full sample of Veterans with OCD, and in the half of the sample with both OCD and PTSD. The tertiary aim is to conduct a mixed-methods formative evaluation of the implementation potential of ERP in VA mental health settings.

NCT ID: NCT05224414 Recruiting - Clinical trials for Obsessive-Compulsive Disorder

Interpretation Bias as a Mechanism of Treatment Response in OCD

Start date: March 30, 2022
Phase: N/A
Study type: Interventional

This study will conduct a randomized controlled trial of Cognitive Bias Modification for Interpretation (CBM-I) as an augmentation to treatment as usual for obsessive compulsive disorder (OCD). CBM-I is a digital intervention designed to directly manipulate interpretation bias through repeated practice on a training task, thereby inducing cognitive changes in a relatively automatic or implicit manner. Specifically, this study will examine the feasibility, acceptability, and clinical outcomes associated with CBM-I. Adults with obsessive compulsive disorder (OCD) will be recruited from a treatment program for this disorder and participants will be randomly assigned to either receive: 1) up to 12 sessions of CBM-I, or or up to 12 sessions of psychoeducation as a control condition.

NCT ID: NCT05221632 Recruiting - Clinical trials for Obsessive-Compulsive Disorder

Accelerated Continue Theta-burst Stimulation (acTBS)Treatment for Obsessive Compulsive Disease

Start date: March 1, 2021
Phase: N/A
Study type: Interventional

The therapeutic effects of high-dose accelerated continue theta-burst stimulation (acTBS) and 1-Hz repetitive transcranial magnetic stimulation (rTMS) on obsessive-compulsive disorder (OCD) and its neural mechanism were investigated by functional MRI.

NCT ID: NCT05166707 Recruiting - Clinical trials for Obsessive-Compulsive Disorder

An ERP-based Mobile Intervention as an Adjunctive Treatment for OCD

Start date: October 18, 2021
Phase: N/A
Study type: Interventional

The objective of this feasibility study is to evaluate the feasibility, acceptability, and potential usefulness of the investigational device, a mobile software application (app) (OC Free) for treatment of OCD (contamination obsession only), adjunctive to individuals receiving outpatient ERP therapy. OC Free is an iOS/Android app that provides treatment via computerized exposure and response prevention (ERP). The study will evaluate preliminary safety and effectiveness of the app using gold-standard, validated 'clinician-administered' and 'self-reporting measures.'

NCT ID: NCT05160129 Recruiting - Clinical trials for Obsessive Compulsive Disorder (OCD)

Connectomic Deep Brain Stimulation for Obsessive Compulsive Disorder

Start date: August 13, 2021
Phase: N/A
Study type: Interventional

Deep brain stimulation (DBS) is an effective treatment for people suffering from severe obsessive-compulsive disorder (OCD) whose symptoms have failed to improve after years and multiple methods of intervention. An effective DBS target for OCD is the anterior limb of the internal capsule (ALIC) brain region. On average 60% of all OCD patients have a clinically significant response to ALIC DBS. However, ALIC DBS may become even more effective with the ability to predict which specific ALIC connections in the brain need to be stimulated for each individual OCD patient. This study therefore investigates personalized stimulation to the ALIC that allows for precise modulation of brain circuits associated with individual OCD symptoms. The study aims to specify the ideal anatomical target for ALIC DBS for maximum therapeutic benefit in each patient.

NCT ID: NCT05048251 Recruiting - Clinical trials for Obsessive-Compulsive Disorder

Individually Targeted Neuromodulation for Contamination-based OCD

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

Patients with obsessive-compulsive disorder (OCD) experience a wide array of different types of obsessions and compulsions. However, current treatments for OCD employ a "one size fits all" approach and are used for all patients regardless of symptom type. In this project, the investigators propose to investigate whether a novel method of transcranial magnetic stimulation specifically reduces contamination/washing symptoms - one of the most common types of OCD.

NCT ID: NCT04978428 Recruiting - Clinical trials for Obsessive-Compulsive Disorder

Epidiolex in Obsessive Compulsive Disorder and Related Disorders

Start date: April 14, 2022
Phase: Phase 2
Study type: Interventional

The primary objective of the proposed study is to evaluate the safety and efficacy of Epidiolex (cannabidiol) in adults with obsessive compulsive and related disorders (OCRDs). Subjects will be treated in an open-label fashion with Epidiolex for two weeks.

NCT ID: NCT04967560 Recruiting - Clinical trials for Obsessive-Compulsive Disorder

The Efficacy and Safety of ALIC/NAcc-DBS for Treatment-refractory OCD

Start date: July 30, 2021
Phase: N/A
Study type: Interventional

The present study aims to explore the efficacy and safety of DBS targeted the combination of the anterior limb of internal capsule and nucleus accumbens (ALIC/NAcc-DBS) to refractory OCD, based on multicenter, randomized, double-blinded, sham-stimulation controlled design, that could help to obtain stronger evidence of the efficacy of multiple targets.

NCT ID: NCT04963257 Recruiting - OCD Clinical Trials

Sertraline Combined With Fluvoxamine in the Treatment of Refractory Obsessive-compulsive Disorder

Start date: January 1, 2020
Phase: Phase 4
Study type: Interventional

To verify that sertraline combined with fluvoxamine is superior to sertraline combined with aripiprazole

NCT ID: NCT04958096 Recruiting - Clinical trials for Obsessive-Compulsive Disorder

Cortical Stimulation to Treat Obsessive Compulsive Disorder

Start date: August 1, 2021
Phase: N/A
Study type: Interventional

The purpose of this study is to identify abnormal brain signals associated with Obsessive Compulsive Disorder (OCD) and psychiatric symptoms and to investigate novel therapeutic stimulation sites. While treating OCD with standard deep brain stimulation (DBS) therapy, the investigators will also monitor the activity of the anterior cingulate and prefrontal cortex, a region known be involved with OCD, decision making, and emotion regulation, and the investigators will identify abnormal activity corresponding to the severity of a patient's OCD. The investigators will also investigate whether it is possible for stimulation delivered to these parts of the brain can improve OCD symptoms. These investigations have the potential to aid in the development of improved forms of DBS that can better target abnormal OCD brain signatures in the future. The investigators will implant a cortical electrode in addition to the ALIC DBS electrode and connect these to an implantable pulse generator that care store field potential data (Medtronic Percept). The decision whether the lead is placed in the prefrontal or cingulate cortex bilaterally will be based upon considerations of the surgical risks for a particular patient based upon their anatomy and the required surgical approach. At multiple time points post-implantation up to 2 years, in our clinic or patient's homes, cortical and subcortical signals will be recorded. Data will be collected while patient are resting or engaged in symptom provocation tasks, emotional/cognitive tasks while cortical stimulation is on and off. In addition to brain signal recordings, symptoms will be assessed using validated questionnaires and tasks to allow identification of neurophysiological correlates of OCD symptoms.