Recruiting NA Generalized Anxiety Disorder

New treatment option for Generalized Anxiety Disorder

Official title Trigeminal Nerve Stimulation in Treatment-resistant Generalized Anxiety Disorder: a Feasibility Study

ClinicalTrials.gov ID: NCT06278909

What this study is testing

What it's testing
This is a feasibility study for trigeminal nerve stimulation (TNS) in patients with treatment-resistant generalized anxiety disorder (TR-GAD). Ten participants will receive TNS for 8 weeks as an augmentation strategy to pharmacological treatment for generalized anxiety disorder (GAD).
  • Which group you join is decided by chance.

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 65

You may be able to join if

  • Meet the Diagnostic and Statistical Manual of Mental Disorders, Fifth Edition (DSM5) criteria for generalized anxiety disorder.
  • people on a stable dose of an selective serotonin reuptake inhibitor (SSRI) or serotonin and noradrenaline reuptake inhibitor (SNRI) for at least 8...
  • Treatment-resistant - treatment resistance will be defined as lack of response to at least two drugs, from two different classes of drugs considered...

You likely can't join if

  • Moderate to severe major depressive disorder
  • Moderate to high suicidality
  • Diagnosis of obsessive compulsive disorder (OCD), PTSD, bipolar disorder, schizophrenia, schizoaffective disorder, personality disorders, substance...
  • Pregnant or breastfeeding women
  • Participants who are experiencing seizures
  • Implanted vagal nerve stimulation (VNS) or other electrical devices
See the full eligibility criteria
Who can join
  • Meet the Diagnostic and Statistical Manual of Mental Disorders, Fifth Edition (DSM5) criteria for generalized anxiety disorder.
  • people on a stable dose of an selective serotonin reuptake inhibitor (SSRI) or serotonin and noradrenaline reuptake inhibitor (SNRI) for at least 8 weeks.
  • Treatment-resistant - treatment resistance will be defined as lack of response to at least two drugs, from two different classes of drugs considered first-line or second-line for GAD. Only trials lasting at least 8...
What rules you out
  • Moderate to severe major depressive disorder
  • Moderate to high suicidality
  • Diagnosis of obsessive compulsive disorder (OCD), PTSD, bipolar disorder, schizophrenia, schizoaffective disorder, personality disorders, substance use disorders, intellectual disabilities and dementia or other...
  • Pregnant or breastfeeding women
  • Participants who are experiencing seizures
  • Implanted vagal nerve stimulation (VNS) or other electrical devices
  • Participants who are already undergoing transcutaneous electrical nerve stimulation
  • Consumption of cannabis, any cannabis by-products, illicit drugs, or alcohol above 3 drinks per week
  • Consumption of natural health products that may affect anxiety or depression symptoms

The study team makes the final eligibility decision.

Where it's taking place

  • Kingston, Ontario, Canada

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 - 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 65 years. The study team makes the final eligibility decision.

Where is this trial taking place?

Study sites include Kingston, Ontario, Canada. Enter your location above to see the nearest site and check your eligibility.

Explore other conditions

BridgeMD is an information and trial-matching tool - not medical advice, and not the study sponsor. Details come from ClinicalTrials.gov; the study team decides eligibility.