Zapping aggression: could a headset tame impulsive outbursts?
NCT ID NCT04732052
First seen Aug 12, 2026 · Last updated Aug 13, 2026 · Updated 1 time
Summary
This clinical trial is testing whether a non-invasive brain stimulation technique called transcranial direct current stimulation (tDCS) can reduce impulsivity and aggression in adults with developmental disabilities. The study will involve 60 participants who have a developmental disability and a recent history of aggressive behavior. Half will receive active tDCS, while the other half will receive a sham (placebo) treatment, to see if the brain stimulation can help lower aggressive symptoms and improve behavior.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- transcranial direct current stimulation (tDCS), a non-invasive brain stimulation device
- What this could lead to
- If effective, tDCS could offer a non-drug, non-invasive way to reduce aggressive behavior and impulsivity in adults with developmental disabilities, potentially improving quality of life and reducing the need for restrictive measures.
- What could go wrong
- This is an early-stage trial with a small number of participants (60), so results may not be conclusive or widely applicable. The treatment may not work for everyone, and there is a risk of side effects, though tDCS is generally considered safe.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
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Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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About 60 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Sep 2022
- Expected to finish
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Dec 2028
An estimate. End dates often move.
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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18 to 65 years
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Adults aged 18-64 years * Diagnosis of a developmental disability * History of one or more incidents of aggression in the last month * Consent to participate in the trial by the individual or their Substitute Decision Maker Exclusion Criteria: * History of epilepsy or seizures * History of acquired brain injury * Having metal in the brain/skull, e.g. splinters, fragments or clips * Having a cochlear implant * Having an implanted neuro-stimulator (e.g. direct brain stimulation, epidural/subdural stimulation, vagal nerve stimulation) * History of brain surgery of procedure * History of severe adverse reaction to tDCS * Having a cardiac pacemaker or intracardiac lines * Current alcohol or drug misuse * Having a sensitive scalp
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The places running it
1 site. The list below names each one and where it is.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Locations
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Providence Care Hospital
RECRUITINGKingston, Ontario, K7L 4X3, Canada
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