Magnetic brain zaps could replace antidepressants for some patients
NCT ID NCT05732298
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study tests whether a non-invasive brain stimulation method called theta burst stimulation can help people with depression who refuse medication. 72 participants will either start treatment right away or wait four weeks. The goal is to see if the stimulation alone can reduce depression symptoms.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- theta burst stimulation (a type of transcranial magnetic stimulation)
- What this could lead to
- If it works, this could offer a drug-free option for people with depression who cannot or will not take antidepressants.
- What could go wrong
- This is a small, early-stage trial with only 72 participants. The treatment is not yet proven, and results may not apply to everyone with depression.
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
-
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
-
About 72 people
The number the study aims to enrol. It can still change while the study runs.
- Started
-
Feb 2023
- Expected to finish
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Mar 2026
An estimate. End dates often move.
- Lead sponsor
-
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 70 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: * uni- or bipolar depression according to ICD-10 * present episode at least four weeks * 18-70 years old * no intake and rejection of anti-depressant medication and * no adequate anti-depressant medication in the present episode * no or stable non-drug anti-depressant treatment (e.g. psychotherapy) * residency in Germany, German speaking Exclusion Criteria: * contraindications for transcranial magnetic stimulation (electric devices or metal parts in the body such as pacemaker * relevant neurological or internistic diseases according to study investigator * participation in other trials during treatment * pregnancy or breatfeeding * legal care and placement in a psychiatric hospital * active suicidality
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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.
Contacts and locations
Locations
-
Department of Psychiatry and Psychotherapy
Regensburg, 93053, Germany
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