Finding Alternatives to Standard Treatment for Attention-Deficit Hyperactivity Disorder

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age9-15
SponsorUniversity of Calgary

About this trial

Attention-Deficit/Hyperactivity Disorder (ADHD) is characterized by poor attention, impulsivity, hyperactivity and emotional-motivational dysregulation. Here, we will test if theta burst repetitive transcranial magnetic stimulation (rTMS) can reduce the symptoms of ADHD.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Diagnosis of ADHD

9-15 years old

IQ greater than 80

English fluency (to enable consent/assent)

Disqualifiers

Diagnosis of mania, psychosis, or bipolar disorder

Impediments to TMS or MRI (i.e. metal implants in body)

Prior electroconvulsive therapy or vagus nerve stimulation

Diagnosis of Autism Spectrum Disorder.

Trial design

Design model

Single group

Treatments tested in this trial

  • rTMS

    Device

    Repetitive transcranial magnetic stimulation (rTMS)

Treatment groups

30 Participants
are divided into 1 treatment group
Group A: Active rTMSExperimental treatment 1 intervention

Trial outcomes

Primary outcomes

1

TEACH-2

Test of everyday attention in children - 2. Direct assessment of attention abilities in children.

Time frame
Baseline to week 5

Secondary outcomes

1

SNAP-18

Parent reporting of ADHD symptom severity

Time frame
5 weeks and 52 weeks.
2

PedsQL

Self reporting of quality of life

Time frame
Baseline to week 5

Other outcomes

Sponsors and contacts

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