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Anxiety DisordersBrain STANDNCT06892847

Brain STimulation for ANxiety and Depression in Youth

A study testing Transcranial Magnetic Stimulation in people with Anxiety Disorders and Depression, run by University of Calgary at 1 site in Canada.

Recruiting

Looking for participants now. Contact the study team or a site below to ask about taking part.

Sites and contacts
Official record
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Trial summary

In this open-label trial, the overall aim is to determine if TMS treatment can improve anxiety and depression in a broad group of children and youth referred by physicians. Read more about this study

Who is it for?
Ages 6 to 18 years
Conditions the study is for
Anxiety Disorders, Depression
What is being tested?
Transcranial Magnetic Stimulation
Type of treatment
Surgery or procedure
Could I receive a placebo?
No, everyone receives an active treatment
How many people
120 participants
Where
1 siteCanada
Study dates
1 Jul 2025to 31 Dec 2028
Phase
Interventional
Are there results?
Not yet: the study is under way

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 6 to 18 years
  • All sexes
  • No healthy volunteers
  • Child, Adult

Who may be able to join

  • aged between 6 and 18 years old
  • diagnosis of anxiety or depression made by a qualified medical professional
  • active anxiety and/or depression symptoms

Who cannot join

  • status epilepticus in past 12-months
  • presence of any disease, medical condition, or physical condition that, in the opinion of the study investigator may compromise, interfere, limit, affect, or reduce the participant's ability to complete the study
  • hospitalization for suicide attempt within the past 3 months (unless participant is under the daily supervision of a physician, such as in a mental health day treatment program)
  • TMS-related contraindications, including implanted medical devices (e.g., pacemaker)
  • if actively taking prescription medication, no changes in medication for at least 3 months prior to entry into the study, with no anticipation of change in the frequency or dose over the duration of the study, unless changes to medication are required for participant safety
  • unable to understand instructions in English

Trial locations and contacts

1 site in 1 country. Contact the study team or a site near you to ask about taking part.

Kara Murias, MD/PhD contact

1 403-441-8411

krmarten@ucalgary.ca

Adrianna Guiffre, PhD contact

adrianna.giuffre1@ucalgary.ca

Canada1 site, 1 recruiting
  • Alberta Children's Hospital

    Calgary, Alberta, T3B 6A8

    Kara Murias, 4038281367, kara.murias@gmail.com

    Recruiting

Other trials in Canada

About this study

Official title: Brain STimulation for ANxiety and Depression in Youth: Brain STAND

In this open-label trial, the overall aim is to determine if TMS treatment can improve anxiety and depression in a broad group of children and youth referred by physicians.

Read the detailed description

Mental health disorders are a leading cause of disability, and approximately 14% of adolescents are diagnosed globally. Within Canada, the prevalence of mental health disorders is increasing, with youth aged 15-24 years being greatly impacted. Broadly, mental health disorders include anxiety, post-traumatic stress disorders, depression, schizophrenia, disruptive behaviour, and neurodevelopmental disorders such as autism spectrum disorder (ASD), and attention-deficit/hyperactivity disorder (ADHD). Mental health disorders are associated with clinically significant disrupted behaviour, emotional regulation, and thinking, and can limit one's ability to participate in activities of daily living and drastically impact quality of life. Moreover, a variety of negative outcomes can be associated with these mental health disorders, including health and development-related concerns regarding educational achievement, substance abuse, violence, reproductive and sexual health. In Canada, suicide was the fourth leading cause of death in children (age 1-14; after cancer, accidental injuries and congenital malformations) and the second leading cause of death in youth (age 15-19; after accidental injury) in 2023 according to Stats Can. https://www150.statcan.gc.ca/.

The literature suggests the peak age of mental health disorder onset within the general global population is 14.5 years; a recent meta-analysis of 192 epidemiological studies also reported approximately 83% of individuals with neurodevelopmental disorders experienced onset by the age of 18 years. Further, approximately 52% of individuals with anxiety or fear-related disorders, 48% with feeding or eating disorders or problems, 45% with obsessive-compulsive or related disorders, 28% with stress disorders, and 12% with mood disorders experienced onset by the age of 18 years. The high prevalence of mental health disorders within the child and youth population, and the limited options and availability of therapy choices is contributing to the need to explore additional treatment opportunities.

Interventions for mental health disorders commonly include psycho-social and pharmacological approaches, though these therapies are largely modelled after adult populations, with some indication that medications are not as effective in children and adolescents. Pharmacotherapy may be accompanied by side-effects, and adverse experiences with psychotropic medications at a young age reportedly contribute to poor long-term adherence to other psychiatric therapies. Many families and patients have strong preference for nonpharmaceutical treatments, which can limit options. Another proposed intervention strategy for mental health disorders involves non-invasive brain stimulation, including transcranial magnetic stimulation (TMS). TMS elicits changes in neural population activation with the use of repetitive TMS (rTMS) or theta-burst stimulation. TMS has been used for the treatment of anxiety and depression in adults, and both TMS and TBS have been well-tolerated in children, with only mild transient side effects noted. TMS may be an effective adjunct or sole treatment for mental health disorders in youth; for example, when combined with antidepressants, rTMS increased the treatment effect in 8-24-year-olds with depression, and therefore the clinical application of TMS for mental health disorders in youth requires further investigation. In the United States, rTMS has been approved for the treatment of depression in adolescents starting at the age of 15, and there are encouraging results in implementation studies in other jurisdictions. To ensure adolescents in Canada have access to this therapy, clinical care pathways (such as appropriate referral criteria, outcome measures, and resource requirements) must be better understood.

There are indications that TMS is effective and safe in many populations that are at high risk of depression. For example, TMS has shown to be safe and effective for treatment of depression during pregnancy. In contrast, the use of antidepressants during pregnancy is associated with a risk (though low) of adverse effects for both mother and fetus. Furthermore, treatment of anxiety and depression in complex populations with co-occurring conditions, such as in patients with neurodevelopmental disorders, has limited research in general and in neurostimulations specifically. Despite the recent approval in the United States, evidence for neurostimulation in children and adolescents is lagging behind that of adults. Given the burden of disease in this population, improvement in research, particularly implementation and clinical integration, is both a clinical and ethical imperative.

Medical subject headings
Anxiety Disorders, Depression

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

Study groups in NCT06892847
Study groupRoleWhat they receive
Transcranial Magnetic Stimulation (TMS)ExperimentalOpen-label study with active TMS for treatment.
Receives: Procedure: Transcranial Magnetic Stimulation

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Revised Children Anxiety and Depression Scale (RCADS)

    This 47-item questionnaire assesses the presence and severity of anxiety and depression symptoms. Items are rated from 0 (never) to 3 (always) and includes six subscales, with higher total scores indicating greater severity of symptoms.

    Measured: Baseline and 5 weeks.

Secondary outcomes (10)
  1. Children's Global Assessment Scale (CGAS)

    This physician-rated scale assesses medical history, symptoms, behaviour, and psychosocial circumstances to determine level of general functioning. A score is entered from 100 (superior functioning) to 0 (needs constant supervision).

    Measured: Baseline and 5 weeks.

  2. PROMIS Pain Interference-8a

    This 8-item questionnaire assesses the impact of pain on aspects of daily living in the past 7 days. Items are rated from 0 (never) to 4 (almost always), with higher scores indicating pain has a greater impact on activities of daily life.

    Measured: Baseline and 5 weeks.

  3. Pediatric Quality of Life Inventory (PedsQL)

    This 28-item questionnaire assesses health-related quality of life in the past month. This tool evaluates multiple domains, including physical, emotional, social, and school functioning. Items are rated from 0 (never) to 4 (almost always), with lower scores indicating greater quality of life.

    Measured: Baseline and 5 weeks

  4. Emotional Dysregulation Inventory (EDI) short form

    This 13-item questionnaire evaluates emotional dysregulation in the past 7 days. This tool is scored from 0 (not at all) to 4 (very severe), with greater scores indicating more emotional dysregulation.

    Measured: Baseline and 5 weeks.

  5. Youth Life Interference Scale (YLIS)

    This 11-item questionnaire assesses the impact of mental health symptoms on daily life in the past 2 weeks. Items are rated from 0 (not at all) to 4 (a great deal), with lower scores indicating mental health symptoms had less impact on daily life.

    Measured: Baseline and 5 weeks.

  6. Pubertal Development Scale (PDS)

    This 5-item questionnaire is used to determine an individual's puberty development category, including pre-pubertal, early pubertal, mid-pubertal, late pubertal, post-pubertal.

    Measured: Baseline

  7. Early Psychosis Screener-26 (EPS-26)

    This 26-item questionnaire assesses symptoms of psychosis, including hallucinations and delusions, in the past 30 days. Items are rated from 1 (never) to 5 (always), with lower scores indicating fewer symptoms of psychosis.

    Measured: Baseline

  8. Strengths and Weaknesses of Attention-Deficit/Hyperactivity Disorder and Normal Behaviour Scale (SWAN)

    This 30-item questionnaire assesses strengths and difficulties with attention and behaviour regulation. This questionnaire compares attention, activity, and impulse to others of similar age, using a scale ranging from far below to far above average.

    Measured: Baseline and 5 weeks.

  9. Aberrant Behavioural Checklist (ABC)

    This 58-item questionnaire assesses behaviour in the past 4 weeks, using a scale from 0 (not at all a problem) to 3 (the problem is severe in degree). This questionnaire includes 5 domains: irritability, hyperactivity, social withdrawal, stereotypic behaviour, and inappropriate speech.

    Measured: Baseline and 5 weeks.

  10. NIH Toolbox Cognition Battery

    This battery assesses attention, executive function, and memory and will be completed in-person on a tablet. Specifically, the List Sorting Working Memory Test, Dimension Change Card Sort Test, Flanker Inhibitory Control and Attention Test, and Picture Sequence Memory Test will be administered and take less than 20 minutes to complete.

    Measured: Baseline and 5 weeks.

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted25 Mar 2025
  2. Study start1 Jul 2025
  3. Primary completion31 Dec 2028 (estimated)
  4. Study completion31 Dec 2028 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Treatment
Allocation
Not applicable
Intervention model
Single group
Model description
Open label
Masking
None (open label)
Enrolment
120 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT06892847
Sponsor's protocol ID
REB25-0288
Acronym
Brain STAND
Status last verified
Jan 2026
First submitted
19 Mar 2025
Last updated
29 Jan 2026
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No

Questions about this trial

What is this clinical trial studying?

A study testing Transcranial Magnetic Stimulation in people with Anxiety Disorders and Depression, run by University of Calgary at 1 site in Canada.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 3 inclusion and 6 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: looking for participants now, as of the sponsor's last update on 29 Jan 2026. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in Canada. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

This study is still under way. Results are not available in the source record yet.

How can a doctor refer a patient or contact the research team?

Contact Kara Murias, MD/PhD (1 403-441-8411, krmarten@ucalgary.ca), or a site near the patient. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Revised Children Anxiety and Depression Scale (RCADS) (time frame: Baseline and 5 weeks.). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 29 Jan 2026.

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