이 페이지는 자동 번역되었으며 번역의 정확성을 보장하지 않습니다. 참조하십시오 영문판 원본 텍스트의 경우.

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

2026년 9월 9일 업데이트: 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.

연구 개요

상태

아직 모집하지 않음

연구 유형

중재적

등록 (추정된)

20

단계

  • 해당 없음

연락처 및 위치

이 섹션에서는 연구를 수행하는 사람들의 연락처 정보와 이 연구가 수행되는 장소에 대한 정보를 제공합니다.

연구 연락처

연구 장소

참여기준

연구원은 적격성 기준이라는 특정 설명에 맞는 사람을 찾습니다. 이러한 기준의 몇 가지 예는 개인의 일반적인 건강 상태 또는 이전 치료입니다.

자격 기준

공부할 수 있는 나이

  • 성인
  • 고령자

건강한 자원 봉사자를 받아들입니다

아니

설명

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

공부 계획

이 섹션에서는 연구 설계 방법과 연구가 측정하는 내용을 포함하여 연구 계획에 대한 세부 정보를 제공합니다.

연구는 어떻게 설계됩니까?

디자인 세부사항

  • 주 목적: 치료
  • 할당: 무작위
  • 중재 모델: 크로스오버 할당
  • 마스킹: 삼루타

무기와 개입

참가자 그룹 / 팔
개입 / 치료
다른: 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.
다른: 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.

연구는 무엇을 측정합니까?

주요 결과 측정

결과 측정
측정값 설명
기간
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.
기간: 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

2차 결과 측정

결과 측정
측정값 설명
기간
To evaluate, in PSP, the effect of anodal tDCS targeting the right GFI on the components of cognitive inhibition assessed by the SST
기간: 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
기간: 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
기간: 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
기간: 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
기간: 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
기간: 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
기간: 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
기간: 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
기간: 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
기간: 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
기간: 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
기간: 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
기간: 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
기간: within 1 hour after each tDCS session
Number of EI and Defects
within 1 hour after each tDCS session
Safety Assessment
기간: within 1 hour after each tDCS session
Grades of EI and Defects
within 1 hour after each tDCS session

공동 작업자 및 조사자

여기에서 이 연구와 관련된 사람과 조직을 찾을 수 있습니다.

연구 기록 날짜

이 날짜는 ClinicalTrials.gov에 대한 연구 기록 및 요약 결과 제출의 진행 상황을 추적합니다. 연구 기록 및 보고된 결과는 공개 웹사이트에 게시되기 전에 특정 품질 관리 기준을 충족하는지 확인하기 위해 국립 의학 도서관(NLM)에서 검토합니다.

연구 주요 날짜

연구 시작 (추정된)

2026년 9월 15일

기본 완료 (추정된)

2028년 7월 15일

연구 완료 (추정된)

2028년 7월 15일

연구 등록 날짜

최초 제출

2026년 7월 7일

QC 기준을 충족하는 최초 제출

2026년 9월 9일

처음 게시됨 (실제)

2026년 9월 14일

연구 기록 업데이트

마지막 업데이트 게시됨 (실제)

2026년 9월 14일

QC 기준을 충족하는 마지막 업데이트 제출

2026년 9월 9일

마지막으로 확인됨

2026년 9월 1일

추가 정보

이 연구와 관련된 용어

개별 참가자 데이터(IPD) 계획

개별 참가자 데이터(IPD)를 공유할 계획입니까?

미정

약물 및 장치 정보, 연구 문서

미국 FDA 규제 의약품 연구

아니

미국 FDA 규제 기기 제품 연구

아니

이 정보는 변경 없이 clinicaltrials.gov 웹사이트에서 직접 가져온 것입니다. 귀하의 연구 세부 정보를 변경, 제거 또는 업데이트하도록 요청하는 경우 register@clinicaltrials.gov. 문의하십시오. 변경 사항이 clinicaltrials.gov에 구현되는 즉시 저희 웹사이트에도 자동으로 업데이트됩니다. .

구독하다