Questa pagina è stata tradotta automaticamente e l'accuratezza della traduzione non è garantita. Si prega di fare riferimento al Versione inglese per un testo di partenza.

Different Frequency Temporal Interference Stimulation on Bilateral Subthalamic Nucleus for Parkinson's Disease

7 agosto 2026 aggiornato da: Ke Dong, MD

A Single-Center, Double-Blind Randomized Controlled Trial of Different Frequency Temporal Interference Stimulation Applied to Bilateral Subthalamic Nucleus for Improving Motor and Vocal Functions in Patients With Parkinson's Disease.

This clinical trial will evaluate the efficacy of accelerated Temporal Interference Stimulation (TIS) as a therapeutic intervention for individuals diagnosed with Parkinson's disease. Different frequency TIS will be delivered targeting the bilateral subthalamic nuclei of the brain according to the patient's clinical symptoms. Specifically, the basal thalamic nuclei on the side opposite to the side where the patient's symptoms are most severe receive stimulation at 130 Hz, whilst those on the other side receive stimulation at 60 Hz. The primary objective is to assess whether accelerated TIS yields measurable improvements in motor performance and verbal speech function among enrolled subjects. Functional magnetic resonance imaging (fMRI) will be adopted as an auxiliary imaging modality to objectively characterize underlying cerebral functional alterations induced by accelerated TIS intervention. The core scientific research questions to be addressed in this trial are listed as follows:

Will different frequency accelerated TIS administered to the bilateral subthalamic nuclei produce significant improvements in motor function and cognitive function among enrolled subjects with Parkinson-related disorders? What quantitative and qualitative modifications in cerebral functional activity will be detected via fMRI after standardized accelerated TIS intervention administration? Investigators will implement a two-arm parallel controlled comparative design for all enrolled eligible subjects. This design remains a parallel design, with two independent groups of subjects receiving different active interventions simultaneously rather than a sham control. All confirmed Parkinson's disease patients will undergo standardized random grouping and be allocated into two independent research arms. Subjects in the experimental arm will receive continuous, standardized TIS intervention targeting bilateral subthalamic nuclei, with the basal thalamic nuclei on the side opposite to the side where the patient's symptoms are most severe receiving stimulation at 130 Hz, and those on the other side receiving stimulation at 60 Hz. Subjects in the control arm will receive continuous, standardized TIS intervention targeting bilateral subthalamic nuclei with bilateral 130 Hz stimulation. The control intervention adopts identical operation procedures, equipment wearing mode and on-site operating environment as the formal TIS intervention, with the only difference being the stimulation frequency setting (bilateral 130 Hz in the control arm versus asymmetric frequency in the experimental arm). Rigorous controlled grouping design will ensure objective, verifiable data support for verifying the actual intervention efficacy of different frequency TIS modes on motor dysfunction and speech impairment in Parkinson-related patients, and will also help to clarify the potential advantages of asymmetric frequency TIS over bilateral same-frequency TIS.

All enrolled subjects will complete the following standardized trial procedures in full compliance with the trial protocol:

Receive continuous targeted intervention of either formal asymmetric frequency TIS (130 Hz on the contralateral side of severe symptoms, 60 Hz on the ipsilateral side) or bilateral 130 Hz TIS control intervention on bilateral subthalamic nuclei, with consecutive 5-day fixed-course administration in strict accordance with trial operating specifications.

Complete unified fMRI brain scanning examinations and standardized motor function as well as speech function quantitative evaluation assessments at two fixed time nodes, including the baseline time point before intervention initiation and the follow-up time point after all intervention courses are completed.

Truthfully record all adverse reactions and abnormal physical discomfort symptoms that occur throughout the whole intervention and follow-up observation cycle in standardized adverse event registration forms.

Panoramica dello studio

Stato

Reclutamento

Condizioni

Intervento / Trattamento

Tipo di studio

Interventistico

Iscrizione (Stimato)

40

Fase

  • Non applicabile

Contatti e Sedi

Questa sezione fornisce i recapiti di coloro che conducono lo studio e informazioni su dove viene condotto lo studio.

Contatto studio

Backup dei contatti dello studio

Luoghi di studio

  • Cina
    • Guangdong
      • Guangzhou, Guangdong, Cina, 510000
        • Reclutamento
        • Department of Rehabilitation Medicine, The First Affiliated Hospital, Sun Yat-sen University
        • Contatto:

Criteri di partecipazione

I ricercatori cercano persone che corrispondano a una certa descrizione, chiamata criteri di ammissibilità. Alcuni esempi di questi criteri sono le condizioni generali di salute di una persona o trattamenti precedenti.

Criteri di ammissibilità

Età idonea allo studio

  • Bambino
  • Adulto
  • Adulto più anziano

Accetta volontari sani

No

Descrizione

Inclusion Criteria:

  1. Idiopathic Parkinson's disease diagnosed by neurologists according to the Movement Disorder Society Clinical Diagnostic Criteria;
  2. Hoehn and Yahr stage 1.5-3.0;
  3. Stable levodopa-based antiparkinsonian medication for at least 4 weeks before enrolment, with no planned medication change during the trial period;
  4. Ability to walk independently;
  5. Ability to understand and follow study instructions and complete the required assessments, with no severe cognitive impairment as screened by the Montreal Cognitive Assessment and/or Mini-Mental State Examination according to prespecified thresholds;
  6. Willingness to participate and provide written informed consent.

Exclusion Criteria:

  1. Any contraindication to MRI or tTIS, including claustrophobia or ferromagnetic intracranial or subcutaneous implants;
  2. Significant systemic disease that could increase study risk or interfere with trial participation;
  3. Neurological disorders other than Parkinson's disease;
  4. Major psychiatric disorder or severe depression or anxiety;
  5. History of deep brain stimulation surgery;
  6. Inability or unwillingness to complete all interventions and assessments.

Piano di studio

Questa sezione fornisce i dettagli del piano di studio, compreso il modo in cui lo studio è progettato e ciò che lo studio sta misurando.

Come è strutturato lo studio?

Dettagli di progettazione

  • Scopo principale: Trattamento
  • Assegnazione: Randomizzato
  • Modello interventistico: Assegnazione parallela
  • Mascheramento: Doppio

Armi e interventi

Gruppo di partecipanti / Arm
Intervento / Trattamento
Sperimentale: Active Stimulation Group
Participants diagnosed with Parkinson's disease in the active stimulation group will receive sequential bilateral subthalamic nucleus (STN) temporal interference electrical stimulation therapy twice daily, with each session lasting 40 minutes and a rest interval of at least 1 hour between treatments. The stimulation target is the bilateral subthalamic nucleus, with individualized electrode placement and current intensity determined via personalized modeling based on each patient's magnetic resonance imaging (MRI) data. For the stimulation protocol, a unified carrier frequency of 2000 Hz is adopted for bilateral STN intervention. Specifically, TI stimulation with an envelope frequency of 130 Hz is delivered to the STN contralateral to the patient's most symptomatic side, while TI stimulation with an envelope frequency of 60 Hz is administered to the STN ipsilateral to the patient's most symptomatic side.
Dispositivo: Temporal Interference Stimulation
Sequential bilateral subthalamic nucleus (STN) temporal interference electrical stimulation, administered twice daily (40 minutes per session, ≥1 hour rest interval between sessions). Stimulation targets are bilateral STN, with individualized electrode placement and current intensity determined via personalized modeling from patient MRI data. A fixed carrier frequency of 2000 Hz is used for all STN stimulation. Specifically, therapeutic temporal interference stimulation with an envelope frequency of 130 Hz is delivered to the STN contralateral to the patient's most symptomatic side, while stimulation with an envelope frequency of 60 Hz is applied to the STN ipsilateral to the most symptomatic side to produce targeted therapeutic interference fields.
Altri nomi:
  • TIS
  • TI
  • ttis
  • TI Stimulation
  • Transcranial Temporal Interference Stimulation
Dispositivo: Temporal Interference Stimulation
Sequential bilateral subthalamic nucleus (STN) temporal interference electrical stimulation (active control), administered twice daily (40 minutes per session, ≥1 hour rest interval between sessions). Stimulation targets are bilateral STN, with individualized electrode placement and current intensity determined via personalized modeling from patient MRI data. The active control stimulation uses two distinct high frequencies (2000 Hz and 2130 Hz) to generate a therapeutic interference field.
Altri nomi:
  • TIS
  • TI
  • ttis
  • TI Stimulation
  • Transcranial Temporal Interference Electrical Stimulation
Comparatore attivo: Active Control Group
Participants diagnosed with Parkinson's disease in the active control group will receive sequential bilateral subthalamic nucleus (STN) temporal interference electrical stimulation therapy twice daily, with each session lasting 40 minutes and a rest interval of at least 1 hour between treatments. The stimulation target is the bilateral subthalamic nucleus, with individualized electrode placement and current intensity determined via personalized modeling based on each patient's magnetic resonance imaging (MRI) data. The active stimulation uses two distinct high frequencies (2000 Hz and 2130 Hz) to generate a therapeutic interference field.
Dispositivo: Temporal Interference Stimulation
Sequential bilateral subthalamic nucleus (STN) temporal interference electrical stimulation, administered twice daily (40 minutes per session, ≥1 hour rest interval between sessions). Stimulation targets are bilateral STN, with individualized electrode placement and current intensity determined via personalized modeling from patient MRI data. A fixed carrier frequency of 2000 Hz is used for all STN stimulation. Specifically, therapeutic temporal interference stimulation with an envelope frequency of 130 Hz is delivered to the STN contralateral to the patient's most symptomatic side, while stimulation with an envelope frequency of 60 Hz is applied to the STN ipsilateral to the most symptomatic side to produce targeted therapeutic interference fields.
Altri nomi:
  • TIS
  • TI
  • ttis
  • TI Stimulation
  • Transcranial Temporal Interference Stimulation
Dispositivo: Temporal Interference Stimulation
Sequential bilateral subthalamic nucleus (STN) temporal interference electrical stimulation (active control), administered twice daily (40 minutes per session, ≥1 hour rest interval between sessions). Stimulation targets are bilateral STN, with individualized electrode placement and current intensity determined via personalized modeling from patient MRI data. The active control stimulation uses two distinct high frequencies (2000 Hz and 2130 Hz) to generate a therapeutic interference field.
Altri nomi:
  • TIS
  • TI
  • ttis
  • TI Stimulation
  • Transcranial Temporal Interference Electrical Stimulation

Cosa sta misurando lo studio?

Misure di risultato primarie

Misura del risultato
Misura Descrizione
Lasso di tempo
The score of the Movement Disorder Society-Unified Parkinson's Disease Rating Scale Part III (MDS-UPDRS-III)
Lasso di tempo: From enrollment to 1 month after treatment
The MDS-UPDRS-III is a standardized assessment tool to evaluate motor function symptoms in people with Parkinson's disease.It has a scoring range of 0 to 132 points, with higher scores meaning more severe motor disorders.
From enrollment to 1 month after treatment

Misure di risultato secondarie

Misura del risultato
Misura Descrizione
Lasso di tempo
The scores of Mini-BESTest
Lasso di tempo: From enrollment to 1 month after treatment
The Mini-BESTest is a clinical assessment tool for evaluating balance function. It assesses the balance control system across multiple domains, with a scoring range of 0 to 28 points; higher scores indicate better balance function.
From enrollment to 1 month after treatment
10-Meter Walk Test
Lasso di tempo: From the enrollment to 1 month after treatment
The 10-Meter Walk Test assesses gait speed and functional mobility by measuring the time required to walk 10 meters. Increased time reflects slower walking and worse mobility.
From the enrollment to 1 month after treatment
BOLD-fMRI
Lasso di tempo: From the enrollment to 1 month after treatment
Functional MRI is used to acquire BOLD data. BOLD signals reflect regional brain activity and functional connectivity. This measure evaluates brain function and structural connectivity associated with motor and cognitive performance.
From the enrollment to 1 month after treatment
Phonation duration
Lasso di tempo: From the enrollment to 1 month after treatment
Phonation duration refers to the continuous time of voluntary phonation. This indicators is used to objectively evaluate the functional status of the subjects' vocal system. Abnormalities in phonation duration may indicate impairments in vocal cord movement, laryngeal muscle control, or related neural regulation, which is of great significance for assessing the severity of vocal function disorders and the effect of intervention.
From the enrollment to 1 month after treatment
Diffusion Tensor Imaging（DTI）
Lasso di tempo: From the enrollment to 1 month after treatment
Functional MRI is used to acquire Diffusion Tensor Imaging（DTI) data. DTI characterizes white matter microstructural integrity and fiber tract organization. This measure evaluates brain function and structural connectivity associated with motor and cognitive performance.
From the enrollment to 1 month after treatment
Voice intensity
Lasso di tempo: From the enrollment to 1 month after treatment
Voice intensity is measured using Praat software. Voice intensity, expressed in dB SPL, reflects the loudness of the voice. This indicators is used to objectively evaluate the functional status of the subjects' vocal system. Abnormalities in voice intensity may indicate impairments in vocal cord movement, laryngeal muscle control, or related neural regulation, which is of great significance for assessing the severity of vocal function disorders and the effect of intervention.
From the enrollment to 1 month after treatment
Velocity of center of pressure (COP) sway
Lasso di tempo: From the enrollment to 1 month after treatment
Center of pressure (COP) sway velocity of subjects on stable and unstable surfaces is measured via a balance board during two standing conditions: single-task quiet standing and dual-task standing. The dual-task standing requires subjects to continuously perform serial subtraction of 7 from random numbers ranging from 400 to 600 while maintaining standing posture. The balance board records COP movement speed under both single-task and dual-task standing states. This indicator objectively assesses balance control and adaptability to different surfaces; abnormal increases indicate impaired balance, aiding evaluation of balance disorder severity and intervention effectiveness.
From the enrollment to 1 month after treatment
Fundamental frequency (F₀)
Lasso di tempo: From the enrollment to 1 month after treatment
Fundamental frequency (F₀) range of subjects' phonation is measured using Praat software. Fundamental frequency range is the interval between the minimum and maximum F₀ (unit: Hz) during phonation, reflecting the variability of voice pitch. This indicators is used to objectively evaluate the functional status of the subjects' vocal system. Abnormalities in F₀ range may indicate impairments in vocal cord movement, laryngeal muscle control, or related neural regulation, which is of great significance for assessing the severity of vocal function disorders and the effect of intervention.
From the enrollment to 1 month after treatment
Range of center of pressure (COP) sway
Lasso di tempo: From the enrollment to 1 month after treatment
Center of pressure (COP) sway range of subjects on stable and unstable surfaces is measured via a balance board during two standing conditions: single-task quiet standing and dual-task standing. The dual-task standing requires subjects to continuously perform serial subtraction of 7 from random numbers ranging from 400 to 600 while maintaining standing posture. The balance board records the maximum displacement range of COP deviation under both single-task and dual-task standing states. This indicator objectively assesses postural stability and balance regulation ability on different surfaces; abnormal increases indicate deteriorated postural control, aiding evaluation of balance disorder severity and intervention effectiveness.
From the enrollment to 1 month after treatment
Path of center of pressure (COP) sway
Lasso di tempo: From the enrollment to 1 month after treatment
Center of pressure (COP) sway path of subjects on stable and unstable surfaces is measured via a balance board during two standing conditions: single-task quiet standing and dual-task standing. The dual-task standing requires subjects to continuously perform serial subtraction of 7 from random numbers ranging from 400 to 600 while maintaining standing posture. The balance board records the total traveling path length of COP movement under both single-task and dual-task standing states. This indicator objectively reflects the complexity and stability of postural adjustment during standing on different surfaces; abnormal increases indicate inefficient balance control and postural instability, aiding evaluation of balance disorder severity and intervention effectiveness.
From the enrollment to 1 month after treatment
Area of center of pressure (COP) sway
Lasso di tempo: From the enrollment to 1 month after treatment
Center of pressure (COP) sway area of subjects on stable and unstable surfaces is measured via a balance board during two standing conditions: single-task quiet standing and dual-task standing. The dual-task standing requires subjects to continuously perform serial subtraction of 7 from random numbers ranging from 400 to 600 while maintaining standing posture. The balance board records the planar enclosed area covered by continuous COP movement under both single-task and dual-task standing states. This indicator objectively evaluates the overall stability of standing posture and anti-interference ability on different surfaces; abnormal increases represent expanded postural sway range and impaired balance function, aiding evaluation of balance disorder severity and intervention effectiveness.
From the enrollment to 1 month after treatment
Timed Up and Go (TUG) Test Time
Lasso di tempo: From the enrollment to 1 month after treatment
The time consumed by subjects to complete the standard Timed Up and Go (TUG) test is recorded as the evaluation outcome. During the test, subjects are required to finish a series of standardized movements including standing up from a chair, straight walking, turning around, and sitting back down independently. This indicator objectively assesses basic walking ability, functional mobility and gross motor control ability of subjects; prolonged completion time indicates impaired walking and mobility function, aiding the evaluation of motor dysfunction severity and intervention effectiveness.
From the enrollment to 1 month after treatment
Dual-Task Timed Up and Go (Dual-Task TUG) Test Time
Lasso di tempo: From the enrollment to 1 month after treatment
The time consumed by subjects to complete the dual-task Timed Up and Go (TUG) test is recorded as the evaluation outcome. During the dual-task test, subjects are required to finish the entire standard TUG motor sequence while simultaneously performing continuous serial subtraction of 7 from random numbers within 100, which imposes additional cognitive load during walking. This indicator comprehensively reflects subjects' dual-task execution ability, integrating walking mobility and cognitive-motor coordination capacity. Increased completion time represents declined dual-task processing efficiency and compromised gait stability under cognitive interference, aiding the evaluation of comprehensive motor-cognitive function and intervention effectiveness.
From the enrollment to 1 month after treatment
The score of the Parkinson's Disease Questionnaire-39 (PDQ-39)
Lasso di tempo: From enrollment to 1 month after treatment
The PDQ-39 is a standardized patient-reported outcome tool to evaluate the health-related quality of life in people with Parkinson's disease. It consists of 39 items covering 8 dimensions (mobility, activities of daily living, emotional well-being, stigma, social support, cognitions, communication, and bodily discomfort), with a scoring range of 0 to 100 points, where higher scores indicate a poorer quality of life.
From enrollment to 1 month after treatment
The score of the Pittsburgh Sleep Quality Index (PSQI)
Lasso di tempo: From enrollment to 1 month after treatment
The PSQI is a standardized assessment tool to evaluate sleep quality and sleep disturbances in people with Parkinson's disease. It has a scoring range of 0 to 21 points, with higher scores indicating more severe sleep disorders.
From enrollment to 1 month after treatment

Collaboratori e investigatori

Qui è dove troverai le persone e le organizzazioni coinvolte in questo studio.

Sponsor

Ke Dong, MD

Studiare le date dei record

Queste date tengono traccia dell'avanzamento della registrazione dello studio e dell'invio dei risultati di sintesi a ClinicalTrials.gov. I record degli studi e i risultati riportati vengono esaminati dalla National Library of Medicine (NLM) per assicurarsi che soddisfino specifici standard di controllo della qualità prima di essere pubblicati sul sito Web pubblico.

Studia le date principali

Inizio studio (Stimato)

20 luglio 2026

Completamento primario (Stimato)

31 dicembre 2026

Completamento dello studio (Stimato)

31 dicembre 2026

Date di iscrizione allo studio

Primo inviato

19 luglio 2026

Primo inviato che soddisfa i criteri di controllo qualità

19 luglio 2026

Primo Inserito (Effettivo)

23 luglio 2026

Aggiornamenti dei record di studio

Ultimo aggiornamento pubblicato (Effettivo)

11 agosto 2026

Ultimo aggiornamento inviato che soddisfa i criteri QC

7 agosto 2026

Ultimo verificato

1 luglio 2026

Maggiori informazioni

Termini relativi a questo studio

Termini MeSH pertinenti aggiuntivi

Altri numeri di identificazione dello studio

  • Nos.82402971

Informazioni su farmaci e dispositivi, documenti di studio

Studia un prodotto farmaceutico regolamentato dalla FDA degli Stati Uniti

No

Studia un dispositivo regolamentato dalla FDA degli Stati Uniti

No

Queste informazioni sono state recuperate direttamente dal sito web clinicaltrials.gov senza alcuna modifica. In caso di richieste di modifica, rimozione o aggiornamento dei dettagli dello studio, contattare register@clinicaltrials.gov. Non appena verrà implementata una modifica su clinicaltrials.gov, questa verrà aggiornata automaticamente anche sul nostro sito web .

Sottoscrivi