Recruiting at 1 site No phase Obsessive Compulsive Disorder (OCD)

Clinical trial for Obsessive Compulsive Disorder (OCD)

Official title OCD LIFU Target Engagement

ClinicalTrials.gov ID: NCT07558148

What this study is testing

What it's testing
This study checks if using low-intensity focused ultrasound on specific brain areas is safe and practical for people with OCD.
Who it's for
People who have Obsessive-Compulsive Disorder (OCD).
What's involved
Participants will receive single sessions of ultrasound treatment on up to three brain targets and fill out questionnaires about their symptoms.
Time commitment
The study involves four visits over a short period to complete the treatments and assessments.

A plain-language read of the study's public ClinicalTrials.gov listing. The study team confirms the details.

Who can take part

Ages 18 to 60

You may be able to join if

  • Adults aged 18-60 years old
  • Chronic OCD (5 years preceding date of enrollment), diagnosed as per the Diagnostic and Statistical Manual of Mental Disorders, Fifth Edition...
  • Presence of obsessions, compulsions, or both time-consuming obsessions and compulsions that take more than one hour a day or cause significant...
  • Disturbance not better explained by the symptoms of another mental disorder listed in the DSM-5 Severe OCD symptoms, as defined by Y-BOCS I score of...
  • Compulsions need to involve movement of the hands and/or arms so that the sleeve is able to detect participant's actions (cannot be solely mental or...

You likely can't join if

  • Unable to undergo MRI scan
  • Presence of metallic implants or devices or tattoos
  • Claustrophobia or severe anxiety
  • Inability to remain still for duration of scan
  • Inability to fit and wear the ATTN201 device for the entire
  • Hearing loss that, in the opinion of the Principal Investigator, an audiologist, or a treating physician, is likely to affect the subject's ability...
See the full eligibility criteria
Who can join
  • Adults aged 18-60 years old
  • Chronic OCD (5 years preceding date of enrollment), diagnosed as per the Diagnostic and Statistical Manual of Mental Disorders, Fifth Edition guidelines (DSM-5)
  • Presence of obsessions, compulsions, or both time-consuming obsessions and compulsions that take more than one hour a day or cause significant distress or impairment in social, occupation, or other important areas of...
  • Disturbance not better explained by the symptoms of another mental disorder listed in the DSM-5 Severe OCD symptoms, as defined by Y-BOCS I score of 28 or higher, within two weeks prior to enrollment
  • Compulsions need to involve movement of the hands and/or arms so that the sleeve is able to detect participant's actions (cannot be solely mental or verbal compulsions)
  • Ability to understand procedure-related instructions and to complete study assessments in English, and ability to comply with protocol requirements (e.g., procedure visits, treatment schedule, follow-up visit schedule...
  • Willingness and ability to provide written agreement to allow any and all forms of communication between the research team and treating clinician(s)
  • Willingness and ability to provide informed consent, in the opinion of the Principal Investigator
What rules you out
  • Unable to undergo MRI scan
  • Presence of metallic implants or devices or tattoos
  • Claustrophobia or severe anxiety
  • Inability to remain still for duration of scan
  • Inability to fit and wear the ATTN201 device for the entire
  • Hearing loss that, in the opinion of the Principal Investigator, an audiologist, or a treating physician, is likely to affect the subject's ability to comply with all of the requirements of the study, or may affect the...
  • Pregnancy - this is an exclusion criterion because we will be intentionally increasing anxiety in participants to evaluate optimal strategies to provoke distress and then promote relaxation
  • Any past or present medical condition, disease, disorder, or injury that, in the opinion of the Principal Investigator, may reduce or hinder the subject's ability to fully comply with all study requirements for the...
  • Have a previous injury or surgery which could affect the nerve distribution
  • Have nerve damage (neuropathy)
  • Have a diagnosed neuromuscular disorder
  • Have a pacemaker
  • Have a history of skin allergies, psoriasis eczema, dermatitis, or other skin inflammation conditions
  • Compulsions cannot be completely mental or verbal actions, such as repeating words, counting objects, or performing mental rituals, and cannot involve only facial muscles/actions such as blinking or staring

The study team makes the final eligibility decision.

Where it is enrolling

  • Philadelphia, Pennsylvania, United States

Questions & answers

Do participants get paid in this trial?

This listing doesn't specify compensation. Many trials still reimburse travel or offer a stipend, so it's worth asking the study team when you connect.

Is it free to join, and do I need insurance?

Searching and applying through BridgeMD is free. In clinical trials the study-related treatment and visits are generally provided at no cost to you. You usually don't need insurance to take part, but confirm specifics with the study team.

How long does this study last?

The listing doesn't state an exact length. The study team walks you through the schedule and number of visits before you decide to enroll.

Who can join this trial?

This study is enrolling all sexes, 18 years to 60 years. The study team makes the final eligibility decision.

Where is this trial taking place?

This study is enrolling now at Philadelphia, Pennsylvania, United States. Enter your location above to see the nearest enrolling site and check your eligibility.

Explore other conditions

BridgeMD is an information and trial-matching tool that is independent of the study sponsor. Details come from ClinicalTrials.gov. The study team decides eligibility, and your own doctor gives medical advice.