Different Frequency Temporal Interference Stimulation on Bilateral Subthalamic Nucleus for Parkinson's Disease
2026年8月7日 更新者：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.
調査の概要
状態
募集
条件
研究の種類
介入
入学 (推定)
40
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
- 名前：Liu Hanjun
- 電話番号：+86 15920175118
- メール：lhanjun@mail.sysu.edu.cn
研究連絡先のバックアップ
- 名前：Dan Zi
- 電話番号：+8618922465578
- メール：925343654@qq.com
研究場所
-
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Guangdong
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Guangzhou、Guangdong、中国、510000
- 募集
- Department of Rehabilitation Medicine, The First Affiliated Hospital, Sun Yat-sen University
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コンタクト：
- Liu Hanjun
- 電話番号：+86 15920175118
- メール：lhanjun@mail.sysu.edu.cn
-
-
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
- 子
- 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:
- Idiopathic Parkinson's disease diagnosed by neurologists according to the Movement Disorder Society Clinical Diagnostic Criteria;
- Hoehn and Yahr stage 1.5-3.0;
- Stable levodopa-based antiparkinsonian medication for at least 4 weeks before enrolment, with no planned medication change during the trial period;
- Ability to walk independently;
- 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;
- Willingness to participate and provide written informed consent.
Exclusion Criteria:
- Any contraindication to MRI or tTIS, including claustrophobia or ferromagnetic intracranial or subcutaneous implants;
- Significant systemic disease that could increase study risk or interfere with trial participation;
- Neurological disorders other than Parkinson's disease;
- Major psychiatric disorder or severe depression or anxiety;
- History of deep brain stimulation surgery;
- Inability or unwillingness to complete all interventions and assessments.
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：並列代入
- マスキング：ダブル
武器と介入
参加者グループ / アーム |
介入・治療 |
|---|---|
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実験的：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.
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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.
他の名前：
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.
他の名前：
|
|
アクティブコンパレータ：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.
|
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.
他の名前：
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.
他の名前：
|
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 |
|---|---|---|
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The score of the Movement Disorder Society-Unified Parkinson's Disease Rating Scale Part III (MDS-UPDRS-III)
時間枠：From enrollment to 1 month after treatment
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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.
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From enrollment to 1 month after treatment
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二次結果の測定
結果測定 |
メジャーの説明 |
時間枠 |
|---|---|---|
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The scores of Mini-BESTest
時間枠：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.
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From enrollment to 1 month after treatment
|
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10-Meter Walk Test
時間枠：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.
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From the enrollment to 1 month after treatment
|
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BOLD-fMRI
時間枠：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.
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From the enrollment to 1 month after treatment
|
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Phonation duration
時間枠：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.
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From the enrollment to 1 month after treatment
|
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Diffusion Tensor Imaging（DTI）
時間枠：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
|
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Voice intensity
時間枠：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
|
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Velocity of center of pressure (COP) sway
時間枠：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
|
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Fundamental frequency (F₀)
時間枠：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
|
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Range of center of pressure (COP) sway
時間枠：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
|
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Path of center of pressure (COP) sway
時間枠：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
|
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Area of center of pressure (COP) sway
時間枠：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
|
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Timed Up and Go (TUG) Test Time
時間枠：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
|
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Dual-Task Timed Up and Go (Dual-Task TUG) Test Time
時間枠：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
|
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The score of the Parkinson's Disease Questionnaire-39 (PDQ-39)
時間枠：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.
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From enrollment to 1 month after treatment
|
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The score of the Pittsburgh Sleep Quality Index (PSQI)
時間枠：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
|
協力者と研究者
ここでは、この調査に関係する人々や組織を見つけることができます。
スポンサー
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7月20日
一次修了 (推定)
2026年12月31日
研究の完了 (推定)
2026年12月31日
試験登録日
最初に提出
2026年7月19日
QC基準を満たした最初の提出物
2026年7月19日
最初の投稿 (実際)
2026年7月23日
学習記録の更新
投稿された最後の更新 (実際)
2026年8月11日
QC基準を満たした最後の更新が送信されました
2026年8月7日
最終確認日
2026年7月1日
詳しくは
この情報は、Web サイト clinicaltrials.gov から変更なしで直接取得したものです。研究の詳細を変更、削除、または更新するリクエストがある場合は、register@clinicaltrials.gov。 までご連絡ください。 clinicaltrials.gov に変更が加えられるとすぐに、ウェブサイトでも自動的に更新されます。