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Zapping a brain region may curb impulsivity in PSP

NCT ID NCT07818733

What the study statuses mean

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Recruitment status, easiest to join first

Recruiting now
This trial is taking on new participants right now.
Not yet recruiting This study
Registered, but not yet taking participants.
By invitation only
Not open to general applications. Only people the study team invites can take part.
Paused
Paused for now. It may or may not start again.
Ongoing
Running, but no longer taking on new participants.
Completed
The trial has finished. Results may not be published yet.
Stopped early
Stopped early, before it reached the end. That can be for many reasons, including safety.
Cancelled
Cancelled before anyone took part.

Expanded access (not trials)

Expanded access
Not a trial. This treatment can be requested outside a study, case by case, for people who qualify.
Expanded access (paused)
Not a trial. The treatment can normally be requested outside a study, but is unavailable right now.
Expanded access (ended)
Not a trial. The treatment could once be requested outside a study, but no longer can.
Approved
The treatment has been approved, so it is available normally rather than through this programme.

When the status isn't known

Details not published
The full record has not been published yet, so there is little to show here.
Status unknown
This status has not been confirmed recently, so it may be out of date.

First seen Sep 14, 2026 · Last updated Sep 15, 2026 · Updated 1 time

Summary

Progressive supranuclear palsy (PSP) causes problems with movement, thinking, and behavior, including impulsivity that can lead to falls. Researchers are testing a non-invasive brain stimulation technique called transcranial direct current stimulation (tDCS) aimed at the right inferior frontal gyrus, a brain area involved in self-control. In this pilot study, 20 patients with PSP will each receive one active and one sham (placebo) tDCS session in random order, one month apart. The team will measure how quickly participants can stop a movement in a computer task, to see if stimulation improves inhibitory control.

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)
What this could lead to
If it works, this could offer a non-drug way to help people with PSP manage impulsivity and thinking problems, and might point to similar help for other brain diseases.
What could go wrong
This is a small pilot study with only 20 people and a single stimulation session. Any benefit may be brief or may not hold up in larger trials, and the procedure may not work for everyone.

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 20 people

The number the study aims to enrol. It can still change while the study runs.

Expected to start

Sep 2026

An estimate. Start dates often move.

Expected to finish

Jul 2028

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

40 to 89 years

Sex

Anyone

Healthy volunteers

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

Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.

Inclusion Criteria: * Aged 40 to 89 years * Patients with probable PSP according to the MDS-9 diagnostic criteria * BREF score \>10; * 18-FDG PET-MRI performed no more than 6 months prior to enrollment and showing: * Glucose hypometabolism defined as \> 2.5 SD compared to an atlas of healthy subjects and * No severe right frontal cortical atrophy according to F Pasquier's global cortical atrophy scale 53 * Concomitant treatments must have been stable for at least 4 weeks prior to enrollment and must remain stable throughout participation * Patient must have provided written informed consent * Patient must be enrolled in a social security program * Patient must be able to understand French and comply with the protocol * Women must use adequate contraceptive measures for the duration of the clinical trial (in accordance with CTFG recommendations) Exclusion Criteria: * Left-handed Patients; * Patients with severe apraxia that interferes with performance of the SST (at the investigator's discretion) * Known visual or hearing impairment that prevents performance of cognitive tests or the stop-signal test; * History of severe psychiatric or neurological disorders other than PSP; * Known significant brain injury(ies) (stroke, tumor, inflammation, post-traumatic, etc.), at the investigator's discretion * Atrophy of the right frontal lobe ≥3 on the F Pasquier Global Cortical Atrophy Scale 53 * History of epilepsy and seizures (or cerebral impairment with unexplained loss of consciousness), severe cardiac disorders, neurosurgical procedures, or severe or frequent headaches; * Presence of a cardiac, neural, drug-delivery, or cerebral stimulator * Presence of cerebral medical devices (such as vascular clips or electronically sensitive devices), intracerebral or intracochlear metal implants, * Patients with any electrically, magnetically, or mechanically activated implant * Patients suffering from a serious, life-threatening condition such as congestive heart failure, chronic obstructive pulmonary disease (COPD), or active neoplasia * Patients with skin conditions (dermatitis, psoriasis, or eczema) or lesions on the scalp or skull that preclude tDCS * Patients under legal guardianship or protective supervision * Pregnant or breastfeeding women * For patients in the ancillary study, contraindication to MRI: Presence of metallic foreign bodies

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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

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  1. The places running it

    1 site. The list below names each one and where it is.

  2. The official record

    ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.

    Open the record ↗

  3. A doctor treating you

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Contacts and locations

Locations

  • CHU de Nantes

    Nantes, Loire Atlantique, 44093, France

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