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Study Evaluating the Effect of Transcranial Direct Current Stimulation (tDCS) Targeting the Right Inferior Frontal Gyrus on Inhibitory Control in Patients With PSP (TinPSP)

2026年9月9日 更新者:Nantes University Hospital

A Double-blind, Randomized, Sham-controlled, Crossover Pilot Study Evaluating the Effect of Transcranial Direct Current Stimulation (tDCS) Targeting the Right Inferior Frontal Gyrus on Inhibitory Control in Patients With PSP.

Progressive supranuclear palsy (PSP) is a rare neurodegenerative disease with a prevalence estimated at 6 per 100,000 in France and a rapidly progressive course. In its classic form (known as the Richardson type), it presents with a predominantly axial Parkinsonian syndrome, postural instability with early falls, oculomotor disorders, and cognitive and behavioral disturbances. Apart from levodopa, which may provide a modest improvement in Parkinsonian syndrome in some patients, the current therapeutic approach relies primarily on rehabilitation techniques, with no proven efficacy.

Cognitive-behavioral symptoms are common in this disease and are primarily characterized by impaired executive functions, linked to dysfunction of the frontal cortex. They often have a devastating effect on quality of life, are associated with an increased risk of falls, and represent a considerable burden for caregivers. Among these symptoms, apathy is the most commonly described symptom. Impulsivity, associated with impaired inhibitory control, is present in 32-74% of cases and may coexist with apathy.

Cognitive and behavioral inhibition depends on a complex brain network that includes, among others, the right inferior frontal gyrus (IFG), the dorsolateral prefrontal cortex, the supplementary motor area, the motor cortex, and the basal ganglia. It has recently been shown that patients with PSP have impaired functional connectivity between the right LFC and other brain structures in the network, and that neurotransmitter deficits in the right LFC correlate with their impulsivity Alongside pharmacological approaches, non-invasive brain stimulation techniques are rapidly expanding as a potential therapeutic tool. Transcranial direct current stimulation (tDCS), by modulating cortical excitability, is a promising technique. It is simple to administer and has demonstrated efficacy in several clinical settings.

Furthermore, a recent meta-analysis of 45 clinical studies shows that single or repeated tDCS sessions could modestly but significantly improve the inhibitory response-measured by reaction time in the stop-signal paradigm-especially when active (anodal) stimulation was applied to the right GFI. These studies primarily involved healthy subjects. A few studies have examined the effects of tDCS in neurodegenerative diseases and in PSP. These studies are still preliminary, involving small sample sizes, but are encouraging. Among these, a randomized study comparing tDCS to sham tDCS demonstrated a beneficial effect of a single-session tDCS session targeting the dorsolateral prefrontal cortex on verbal fluency in patients with PSP.

The hypothesis of our study is that applying tDCS stimulation over the right GFI will improve certain cognitive functions and reduce behavioral impulsivity in patients.

Very little data on tDCS in PSP is available to date. Only three studies have been published. With very different designs-including only one randomized trial comparing tDCS to sham tDCS-these studies evaluated the effects of tDCS applied to the dorsolateral prefrontal cortex or to motor and premotor areas on language and motor symptoms, respectively.

In this randomized, double-blind, controlled study, the investigators propose to explore the effects of tDCS on the right GFI on executive functions and, more specifically, on inhibitory control. Another strength of our study is that only patients with proven frontal cerebral hypometabolism on FDG-PET-MRI will be included, which will allow us to test the effect of tDCS on a clearly dysfunctional neural network. Furthermore, as a secondary objective, the investigators will be able to assess whether the effects of tDCS depend on the intensity and/or topography of cerebral hypometabolism.

The neurophysiological effects of a single tDCS session appear to last up to 60 to 90 minutes. In this proof-of-concept study, the assessment tests were deliberately chosen for their short administration time and low test-retest effect. Finally, the Stop Signal Test, already used in this population, is widely used and well-standardized.

This pilot study will provide initial data on the cognitive and motor effects of a tDCS session on the GFI, with a focus on inhibition. Given the limited effectiveness of symptomatic treatments-particularly pharmacological ones-having a new option capable of improving cognitive and/or behavioral performance would have a significant impact on the quality of life of patients and their families. tDCS has the advantage of being easily accessible and generally well-tolerated by patients and could eventually be administered in patients' homes.

If our study demonstrates an improvement in certain cognitive/motor functions, it would lead to a larger-scale study with repeated sessions to assess its benefits over a longer period.

Finally, if an improvement in executive functions is demonstrated in PSP, this could apply to other neurodegenerative diseases.

調査の概要

研究の種類

介入

入学 (推定)

20

段階

  • 適用できない

連絡先と場所

このセクションには、調査を実施する担当者の連絡先の詳細と、この調査が実施されている場所に関する情報が記載されています。

研究連絡先

研究場所

参加基準

研究者は、適格基準と呼ばれる特定の説明に適合する人を探します。これらの基準のいくつかの例は、人の一般的な健康状態または以前の治療です。

適格基準

就学可能な年齢

  • 大人
  • 高齢者

健康ボランティアの受け入れ

いいえ

説明

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

研究計画

このセクションでは、研究がどのように設計され、研究が何を測定しているかなど、研究計画の詳細を提供します。

研究はどのように設計されていますか?

デザインの詳細

  • 主な目的:処理
  • 割り当て:ランダム化
  • 介入モデル:クロスオーバー割り当て
  • マスキング:トリプル

武器と介入

参加者グループ / アーム
介入・治療
他の:tDCS Active (first visit) + tDCS sham (second visit)
Each participant will receive active tDCS then sham tDCS during two 20-minute sessions spaced one month apart
Each participant will receive both active tDCS and sham tDCS during two 20-minute sessions spaced one month apart, with the order of the sessions determined at random.
他の:sham tDCS (fist visit) + active tDCS (second visit)
Each participant will receive sham tDCS then active tDCS during two 20-minute sessions spaced one month apart
Each participant will receive both active tDCS and sham tDCS during two 20-minute sessions spaced one month apart, with the order of the sessions determined at random.

この研究は何を測定していますか?

主要な結果の測定

結果測定
メジャーの説明
時間枠
To evaluate the effect of anodal tDCS targeting the right inferior frontal gyrus (IFG) on a motor-modality cognitive inhibition task, the Stop Signal Task (SST), in patients with PSP.
時間枠:during the hour before each tDCS session and within 1 hour after each tDCS session
Stop Signal Reaction Time (SSRT) during the SST (seconds)
during the hour before each tDCS session and within 1 hour after each tDCS session

二次結果の測定

結果測定
メジャーの説明
時間枠
To evaluate, in PSP, the effect of anodal tDCS targeting the right GFI on the components of cognitive inhibition assessed by the SST
時間枠:during the hour before each tDCS session and within 1 hour after each tDCS session
Results for each of the two conditions (active / sham) regarding the components of cognitive inhibition in the stop-signal test: reaction time (seconds), number of failed inhibitions, and number of unresponded-to Go stimuli will be combined to obtain a grade (low/high)
during the hour before each tDCS session and within 1 hour after each tDCS session
To evaluate, within the PSP, the effect of anodal tDCS targeting the right GFI on scores on the following neuropsychological assessments of verbal cognitive inhibition
時間枠:during the hour before each tDCS session and within 1 hour after each tDCS session
Results for each of the two conditions (active / sham) on the Color Word Interference test from the Delis Kaplan Executive System (or Stroop D-KEFS)(scale: Preserved executive functions-Difficulty adapting to novelty)
during the hour before each tDCS session and within 1 hour after each tDCS session
To evaluate, within the PSP, the effect of anodal tDCS targeting the right GFI on scores on the following neuropsychological assessments of perseverative motor behavior
時間枠:during the hour before each tDCS session and within 1 hour after each tDCS session
Results for each of the two conditions (active / sham) regarding the presence or absence of an applause sign and the presence or absence of palilalia
during the hour before each tDCS session and within 1 hour after each tDCS session
To evaluate, within the PSP, the effect of anodal tDCS targeting the right GFI on scores on the following neuropsychological assessments of other executive functions
時間枠:during the hour before each tDCS session and within 1 hour after each tDCS session
Results for each of the two conditions (active / sham) on the Phonological and Categorical Verbal Fluency Test-which measures perseverations and clusters-and the Symbol-Digit Modality Test.
during the hour before each tDCS session and within 1 hour after each tDCS session
To evaluate, within the PSP, the effect of anodal tDCS targeting the right GFI on scores on the following neuropsychological assessments of social cognition
時間枠:during the hour before each tDCS session and within 1 hour after each tDCS session
Results for each of the two conditions (active / sham) on the modified Ekman Emotion Recognition Test (6 emotions).
during the hour before each tDCS session and within 1 hour after each tDCS session
To evaluate, within the PSP, the effect of anodal tDCS targeting the right GFI on scores on the following neuropsychological assessments of overall cognitive efficiency
時間枠:during the hour before each tDCS session and within 1 hour after each tDCS session
Results for each of the two conditions (active / sham) on the MoCA
during the hour before each tDCS session and within 1 hour after each tDCS session
To evaluate, in the PSP, the effect of anodal tDCS targeting the right GFI on motor and bulbar symptoms
時間枠:during the hour before each tDCS session and within 1 hour after each tDCS session
Results for each of the two conditions (active / sham) on the PSP-RS scale subscores (ocular motility, bulbar examination, limb examination, gait examination)
during the hour before each tDCS session and within 1 hour after each tDCS session
To evaluate the effect of anodal tDCS targeting the right GFI on motor function in PSP
時間枠:during the hour before each tDCS session and within 1 hour after each tDCS session
Results for each of the two conditions (active / sham) on the Timed Up and Go Test
during the hour before each tDCS session and within 1 hour after each tDCS session
To analyze the effects of tDCS on brain metabolism patterns as assessed by 18-FDG PET-MRI
時間枠:before and after each tDCS session
Effect of tDCS as described in Sections 3 and 4 and the brain binding pattern of the FDG tracer in PET-MRI
before and after each tDCS session
To evaluate the clinical effects of tDCS on patients' clinical characteristics
時間枠:Baseline, before and after each tDCS session
Effect of tDCS as described in Sections 3 and 4, and baseline scores on the PSP-RS scales
Baseline, before and after each tDCS session
To evaluate the clinical effects of tDCS on patients' clinical characteristics
時間枠:Baseline, before and after each tDCS session
Effect of tDCS as described in Sections 3 and 4, and baseline scores on the BREF scales
Baseline, before and after each tDCS session
To evaluate the clinical effects of tDCS on patients' clinical characteristics
時間枠:Baseline, before and after each tDCS session
Effect of tDCS as described in Sections 3 and 4, and baseline scores on the NPI scale
Baseline, before and after each tDCS session
Assess participants' perception and acceptance of tDCS stimulation
時間枠:within 1 hour after each tDCS session
Number and severity of targeted symptoms (itching, burning, pain, etc.) based on the structured questionnaire developed by Antal et al.40
within 1 hour after each tDCS session
Safety Assessment
時間枠:within 1 hour after each tDCS session
Number of EI and Defects
within 1 hour after each tDCS session
Safety Assessment
時間枠:within 1 hour after each tDCS session
Grades of EI and Defects
within 1 hour after each tDCS session

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研究記録日

これらの日付は、ClinicalTrials.gov への研究記録と要約結果の提出の進捗状況を追跡します。研究記録と報告された結果は、国立医学図書館 (NLM) によって審査され、公開 Web サイトに掲載される前に、特定の品質管理基準を満たしていることが確認されます。

主要日程の研究

研究開始 (推定)

2026年9月15日

一次修了 (推定)

2028年7月15日

研究の完了 (推定)

2028年7月15日

試験登録日

最初に提出

2026年7月7日

QC基準を満たした最初の提出物

2026年9月9日

最初の投稿 (実際)

2026年9月14日

学習記録の更新

投稿された最後の更新 (実際)

2026年9月14日

QC基準を満たした最後の更新が送信されました

2026年9月9日

最終確認日

2026年9月1日

詳しくは

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