CClinicalTrials.gg
Status unknownNCT05404360Updated Jul 20, 2022

Evaluation of the Long Term Efficacy and Durability of the BrainsWay Deep TMS in OCD Subjects

An interventional study of BrainsWay Deep TMS HAC/H7-Coil and BrainsWay Deep TMS Sham Coil in Obsessive-Compulsive Disorder, sponsored by Brainsway. Status unknown. Open to participants aged 18 Years to 88 Years. Per ClinicalTrials.gov, last updated 2022-07-20.

Sponsored by Brainsway · Not applicable, Interventional, and Treatment

The sponsor has not verified this record recently (last verified Jul 2022), so the status shown — last known as Not yet recruiting — may be out of date.
Phase
Not applicable
Study type
Interventional
Enrollment
124
Allocation
Randomized
Ages
18 Years to 88 Years
Sex
All
01

Study summary

A Prospective Double Blind Randomized Controlled Trial to Evaluate the Long Term Efficacy and Durability of the BrainsWay Deep Transcranial Magnetic Stimulation (Deep TMS) in Obsessive-Compulsive Subjects

Read the detailed description

The study is a randomized, double-blind, multi-center trial comparing active Deep TMS treatment to sham treatment over the course of the trial. The treatment phase will consist of 44 treatments over thirteen weeks. The acute treatment phase will consist five daily treatments over the course of six weeks, followed by twice weekly continuation treatments for seven weeks. Responders will be eligible to enter the durability phase. For assessment of durability, responders will be assessed quarterly for up to one year from the end of the treatment phase.

02

Conditions studied

  • Obsessive-Compulsive Disorder
03

Who can participate

Ages eligible
18 Years to 88 Years
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

  • Outpatients
  • Males and females, 18-88 years of age
  • Diagnosed as suffering from OCD according to the DSM-V.
  • Subjects with a YBOCS score of >20.
  • If on SRI, patient must be maintained on current dosages (with or without additional antidepressant or psychotropic augmentation for treatment of OCD), at a stable therapeutic dosage for at least 2 months prior to study entry and for the duration of the trial.
  • If in CBT, must be in the maintenance stage (i.e., not receiving active training in exposure and response prevention, which is the core component of this treatment). CBT can be with teletherapy but must be for a minimum of ten sessions with a symptom checklist, hierarchy, with exposure and response prevention therapy.
  • Have negative or justified responses by the investigator to all questions listed on the Transcranial Magnetic Stimulation Safety Screening questionnaire (TASS).
  • According to the treating physician the subject is compliant with taking medication, if applicable.
  • Subject is capable and willing to provide informed consent and assent.
  • Willing and able to adhere to the treatment schedule.
  • Must own a smartphone.
  • All comorbid diagnoses have been stable for 3 months and anticipated to be stable for the 3 months treatment duration.

Exclusion criteria

Exclusion Criteria:

  • Subjects diagnosed as suffering from any other Axis I diagnosis as the primary diagnosis.
  • Comorbid, secondary psychiatric diagnoses are unstable and are likely to require changes in therapeutic regimens even if OCD improves.
  • Present suicidal risk as assessed by the investigator using the Columbia Suicide Severity Rating Scale, brief mental status exam and psychiatric interview or a history of attempted suicide in the past year.
  • History of epilepsy or seizure (EXCEPT those therapeutically induced by ECT and febrile seizures in infancy).
  • Increased risk of seizure for any reason, including prior diagnosis of increased intracranial pressure, or history of significant head trauma with loss of consciousness for greater than or equal to 5 minutes.
  • History of head injury necessitating cranial surgery or prolonged coma.
  • History of any ferromagnetic of conductive material in the head including the eyes and ears (outside the mouth).
  • Known history of any metallic particles in the eye, implanted neurostimulators, intracranial implant (e.g., aneurysm clips, shunts, stimulators, cochlear implants, or electrodes).
  • History of significant hearing loss.
  • Subjects with significant neurological disorder or insult including, but not limited to
  • Any condition likely to be associated with increased intracranial pressure
  • Space occupying brain lesion
  • History of cerebrovascular accident
  • Transient ischemic attack within two years
  • Cerebral aneurysm
  • Multiple sclerosis
  • Substance use disorder within the past 6 months (except nicotine and caffeine).
  • Currently participating in another therapeutic clinical study.
  • Suffer from an unstable physical, systemic and metabolic disorder such as unstable blood pressure, unstable blood sugar, or acute, unstable cardiac disease.
  • Subject on high doses of antidepressant or psychotropic medications, which are known to lower the seizure threshold. Subject is currently on Clomipramine.
  • Significant possibility of death within eighteen months of baseline.
  • Planned surgeries that will interrupt the study schedule within eighteen months of baseline
  • Treatment with any TMS in the past year.
  • Women who are breast-feeding.
  • Women who are pregnant or with suspected pregnancy.
  • Women of childbearing potential and not using a medically accepted form of contraception when engaging in sexual intercourse.
04

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Triple (Participant, Care provider, Investigator)
Enrollment
124 participants (estimated)

Study arms

  • Experimental
    Treatment Group

    During the acute treatment phase, subjects will receive daily prefrontal Deep TMS treatment, 5 days a week for 6 consecutive weeks. Following the acute phase, patients will receive semi-weekly Deep TMS stimulation for an additional seven weeks. Treatment will include a total of 44 treatments over 13 weeks.

    Device: BrainsWay Deep TMS HAC/H7-Coil

  • Sham comparator
    Sham Control Group

    During the acute treatment phase, subjects will receive daily prefrontal sham treatment, 5 days a week for 6 consecutive weeks. Following the acute phase, patients will receive semi-weekly sham stimulation for an additional seven weeks. Treatment will include a total of 44 treatments over 13 weeks.

    Device: BrainsWay Deep TMS Sham Coil

Interventions

  • DeviceBrainsWay Deep TMS HAC/H7-Coil

    The BrainsWay HAC/H7-Coil Deep TMS System is composed of four main components: an electromagnetic H7/HAC-Coil, TMS stimulator, cooling system and positioning arm.

    Also known as: Active Treatment

  • DeviceBrainsWay Deep TMS Sham Coil

    The experimental system has two coils in the same helmet, a sham and active coil. The sham coil has a similar acoustic artifact as the active coil and it administers a superficial stimulation to maintain blinding. The system assigns the active or sham coil based on the patient ID during the high frequency treatment.

05

What researchers measure

Primary outcomes

  1. Yale Brown Obsessive Compulsive Scale (YBOCS)

    Change in YBOCS scores from baseline to the end of six weeks between the active Deep TMS and Sham treatment groups. Scores on the YBOCS range from 0 (no Symptoms) to 40 (Extreme Symptoms).

    Time frame: 6 weeks

  2. Yale Brown Obsessive Compulsive Scale (YBOCS)

    Change in YBOCS scores from baseline to the end of thirteen weeks between the active Deep TMS and Sham treatment groups. Scores on the YBOCS range from 0 (no Symptoms) to 40 (Extreme Symptoms).

    Time frame: 13 weeks

06

Study locations

No study locations are listed for this record.

07

Registry details

Key details

Study ID
NCT05404360
Lead sponsor
Brainsway
Responsible party
Sponsor
First posted
Jun 3, 2022
Start date
Aug 2022 (estimated)
Primary completion
Jun 2024 (estimated)
Completion
Jun 2024 (estimated)
Last update
Jul 20, 2022

Study contacts

Ahava Stein
Contact
ahava@asteinrac.com
97297670002
Lisa Bokobza
Contact
lisa@asteinrac.com
97297670002

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
Yes
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is status unknown, as verified in Jul 2022. You cannot join it, but the record below documents what was studied.

Follow this study

Get an email when the registry record changes — status, dates, results — or when someone posts here.

Sign in to follow

Discussion

Questions and observations about this study, from anyone following it. Not medical advice, and not a channel to the study team — their contact details are on the registry record.

Sign in to join the discussion. Reading takes no account; posting does. You choose a display name, and a pseudonym is the default.

Nothing here yet. If you are running this trial, taking part in it, or weighing whether to, this is the place to say so.

Start the discussion