Effect of Cerebellar Fastigial Nucleus Stimulation Combined With Sling Exercise on Motor Function in Hemiplegic Stroke Patients
Effects of Cerebellar Fastigial Nucleus Electrical Stimulation Combined With Sling Exercise Therapy on Motor Function in Hemiplegic Patients After Stroke
Przegląd badań
Status
Status
Warunki
Warunki
Interwencja / Leczenie
Interwencja / Leczenie
Szczegółowy opis
This study delivers an in-depth technical and mechanistic elaboration of a novel central-peripheral synergistic rehabilitation paradigm for post-stroke hemiplegia, focusing on the combined application of Fastigial Nucleus Stimulation (FNS) and Sling Exercise Training (SET). It primarily expands on the neurophysiological rationale, technical intervention characteristics, synergistic working mechanisms, optimized trial design logic, standardized quality control and core innovative connotations of the combined intervention, avoiding repetitive descriptions of basic trial elements including participant eligibility, outcome measures, sample size calculation and statistical analysis plans. Targeting the key technical bottleneck of conventional post-stroke rehabilitation-non-specific central neural regulation and superficial muscle activation that fails to reverse pathological neural plasticity-this study focuses on the core deficit of cerebello-thalamo-cortical circuit dysfunction and insufficient deep sensorimotor pathway activation, aiming to develop a targeted, high-efficiency combined rehabilitation technical system.
Persistent motor dysfunction after stroke is not limited to superficial limb movement impairment, but essentially stems from defective central motor regulation and disrupted trunk deep sensorimotor integration. Conventional physical therapy mainly concentrates on passive joint protection and superficial limb functional training, which can only prevent secondary complications such as muscle atrophy and joint contractures. However, it lacks targeted modulation of the central balance and motor coordination hub, and cannot reverse stroke-induced neural plasticity inhibition. This leads to persistent deficits in core stability, proprioceptive acuity and dynamic balance, fundamentally restricting the recovery of fine motor skills and daily living function. To address this clinical technical gap, the present study constructs a bidirectional rehabilitation loop integrating precise central neuromodulation and high-sensitivity peripheral sensorimotor training, realizing organic combination of central neural priming and peripheral sensory feedback remodeling.
FNS is a refined, anatomically targeted non-invasive cerebellar neuromodulation technique with unique advantages over broad cortical stimulation modalities. It precisely targets the fastigial nucleus, the core functional node of the cerebellar motor regulatory network, to specifically activate the cerebello-thalamo-cortical neural circuit. This intervention upregulates the excitability of motor-associated cortical regions, enhances local cerebral microperfusion in motor functional areas, and reverses the post-stroke inhibitory state of endogenous neural plasticity. The high-frequency, low-intensity stimulation paradigm adopted in this study is technically optimized for stroke neural repair. It stably induces activity-dependent neural remodeling without triggering cortical over-excitation or neural fatigue, effectively improving the central nervous system's capacity for sensory information integration and precise motor command output, and building a favorable neurophysiological microenvironment for peripheral motor function reconstruction.
SET represents an upgraded sensorimotor integration training technology that breaks the inherent limitations of traditional planar rehabilitation training. By creating an unstable suspension mechanical environment, SET actively triggers autonomous fine regulation of deep trunk stabilizers, including the transversus abdominis and multifidus muscles, which are rarely activated by conventional training methods. The continuous unbalanced mechanical stimulation generated during training elicits high-density proprioceptive afferent signals from trunk and limb muscles, tendons and joints, activates complete human closed kinetic chains, and drives use-dependent functional reorganization of the sensorimotor cortex. Compared with conventional peripheral training, SET significantly improves the accuracy of somatic sensory input and the efficiency of neuromuscular recruitment, serving as a core technical means to improve dynamic balance, trunk control and gait symmetry in post-stroke patients.
The prominent technical innovation of this research lies in the "central priming + peripheral reinforcement" synergistic intervention mechanism, which targets the self-perpetuating pathological vicious cycle of post-stroke motor dysfunction. Central circuit damage after stroke disrupts normal motor command generation, inducing peripheral disuse muscle atrophy and proprioceptive degradation; in turn, distorted peripheral sensory feedback fails to provide effective remodeling stimuli for the central nervous system, further aggravating motor control disorders. The combination of FNS and SET effectively interrupts this pathological cycle. FNS pre-activates and primes the central cerebello-thalamo-cortical pathway to enhance central neural sensitivity to peripheral sensory signals. On this optimized central neural basis, SET delivers high-fidelity, multi-dimensional proprioceptive afferent input, which acts on the primed central circuit, strengthens synaptic connection efficacy via Hebbian plasticity, and produces superposed and amplified therapeutic effects-achieving a genuine synergistic "1+1>2" effect beyond the simple additive efficacy of single interventions.
A rigorous randomized, double-blind, sham-controlled parallel-group design is adopted in this study to ensure objective and accurate verification of the synergistic therapeutic effect, with optimized sham intervention settings to eliminate systematic bias. The sham FNS protocol applies subthreshold low-intensity current that produces identical cutaneous sensory perception without activating neuronal circuits, while sham SET maintains consistent suspension posture and environmental conditions as active training but excludes voluntary neuromuscular contraction. This standardized double sham-control system effectively isolates placebo effects and individual intervention efficacy, enabling accurate differentiation of the independent therapeutic contributions of FNS-mediated central neuromodulation and SET-mediated peripheral sensorimotor training, and providing reliable technical verification for the specific synergistic effect of central-peripheral co-intervention.
All intervention procedures implement unified standardized technical specifications to ensure trial homogeneity and reproducibility. FNS stimulation adopts standardized bilateral mastoid positioning to precisely target fastigial nucleus projection areas, with all stimulation parameters optimized based on existing neuromodulation mechanism evidence to guarantee stable and effective central neural priming. All SET interventions are delivered by professionally certified rehabilitation therapists, with real-time individualized adjustment of training difficulty based on patients' motor control level and fatigue status. The progressive unstable suspension training mode ensures sustained, graded sensorimotor stimulation, avoiding the dual defects of insufficient stimulus intensity and excessive training load existing in fixed conventional training protocols.
A full-process safety and quality control system is established to standardize intervention implementation and protect participant safety. For FNS neuromodulation, real-time sensory monitoring is conducted throughout stimulation sessions; mild adverse reactions such as local tingling and headache are managed by parameter adjustment or temporary stimulation suspension to ensure good neurological tolerance. For SET training, pre-experiment equipment safety inspection and whole-process therapist supervision are mandatory to prevent muscle strain, excessive fatigue and fall risks. Individualized training intensity matching is implemented for patients with different motor function levels to balance training efficacy and safety. All adverse events are recorded in detail and managed hierarchically to ensure standardized and consistent trial implementation.
In summary, this study focuses entirely on technical innovation, neurophysiological mechanisms and synergistic principles of combined central-peripheral rehabilitation, without redundant description of routine trial baseline elements. Its core research value lies in elucidating the synergistic rehabilitation mechanism between fastigial nucleus central neuromodulation and deep core peripheral sensorimotor activation, establishing a standardized, safe and minimally invasive combined rehabilitation technical system, and providing high-level mechanistic and clinical evidence for optimizing individualized rehabilitation strategies for post-stroke hemiplegia.
Typ studiów
Typ studiów
Zapisy (Szacowany)
Zapisy
Faza
Faza
- Nie dotyczy
Kontakty i lokalizacje
Kontakt w sprawie studiów
Kontakt w sprawie studiów
- Nazwa: Xue Jiang
- Numer telefonu: +8618940254064
- E-mail: jiangxueruby@163.com
Kopia zapasowa kontaktu do badania
- Nazwa: Mengyuan Yu
- Numer telefonu: +8619537240701
- E-mail: Decads0110@qq.com
Lokalizacje studiów
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Shenyang, Chiny
- Rehabilitation Center of Shengjing Hospital, China Medical University, shenyang, Liaoning 110000
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Kontakt:
- Xue Jiang
- Numer telefonu: +86 189 4025 4064
- E-mail: jiangxueruby@163.com
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Kontakt:
- Mengyuan Yu
- Numer telefonu: +8619537240701
- E-mail: Decads0110@qq.com
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Kryteria uczestnictwa
Kryteria kwalifikacji
Kryteria kwalifikacji
Wiek uprawniający do nauki
- Dorosły
- Starszy dorosły
Akceptuje zdrowych ochotników
Opis
Inclusion Criteria:
- Met the diagnostic criteria for cerebrovascular disease in Western medicine;
- Were conscious, with stable vital signs and emotional state;
- Were male or female, aged 18 to 70 years, with disease onset within the previous 6 months;
- Had no significant cognitive or auditory comprehension impairments, were able to understand and execute relevant instructions, and could cooperate with the completion of relevant rehabilitation assessments;
- Were informed about the study and had signed an informed consent form.
Exclusion Criteria:
- Presence of severe organ dysfunction involving the cardiovascular, pulmonary, liver, or renal systems;
- Severe joint diseases, incompletely healed fractures, or severe osteoporosis;
- History of psychiatric illness or severe cognitive, visual, or auditory comprehension impairments that would prevent cooperation with instructions;
- Concurrent vestibular dysfunction;
- Unstable vital signs;
- Patients requiring mechanical ventilation;
- Contraindications to FNS, such as a history of epilepsy or the presence of intracranial metal foreign bodies.
Plan studiów
Jak projektuje się badanie?
Szczegóły projektu
- Główny cel: Leczenie
- Przydział: Randomizowane
- Model interwencyjny: Przydział równoległy
- Maskowanie: Pojedynczy
Liczba ramion
Broń i interwencje
Grupa uczestników / ArmGrupa uczestników / Arm |
Interwencja / LeczenieInterwencja / Leczenie |
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Eksperymentalny: Group A: FNS + sham SET training
FNS: High-precision electrodes were used, with the treatment electrodes placed posterior to the mastoid processes on both sides. The stimulation parameters were set at a frequency of 180 Hz and an intensity of 2 mA for 20 minutes. Sham SET training: Patients were only fixed with non-elastic ropes following the SET training method described above, without performing any movements. This was conducted once daily for 30 minutes. |
Participants received group-specific interventions 5 days/week for 4 weeks.
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Eksperymentalny: Group B: sham FNS + SET
Sham FNS: Electrodes were placed in the same position (bilaterally posterior to the mastoid processes). The output was set to a subthreshold intensity (0.1 mA, 180 Hz, 20 min) insufficient to alter neuronal excitability but sufficient to maintain a sense of contact. SET: ① Supine bridge: Patient in supine position, ankles fixed with non-elastic ropes. Patient lifts hips to align with trunk. Hold for 10 s, rest for 5 s; 15 repetitions per set, 2 sets. ② Prone bridge: Patient in prone position, ankles suspended with non-elastic ropes to lift feet off the bed. With therapist assistance, patient lifts hips to maintain a horizontal body position. Hold for approximately 10 s, rest for 5 s; 15 repetitions per set, 2 sets. The exercise difficulty was selected and adjusted in a timely manner based on the patient's condition, performance during training, and subjective feedback. |
Participants received group-specific interventions 5 days/week for 4 weeks.
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Eksperymentalny: Group C: FNS +SET
FNS: High-precision electrodes were used, with the treatment electrodes placed posterior to the mastoid processes on both sides. The stimulation parameters were set at a frequency of 180 Hz and an intensity of 2 mA for 20 minutes. SET: ① Supine bridge: Patient in supine position, ankles fixed with non-elastic ropes. Patient lifts hips to align with trunk. Hold for 10 s, rest for 5 s; 15 repetitions per set, 2 sets. ② Prone bridge: Patient in prone position, ankles suspended with non-elastic ropes to lift feet off the bed. With therapist assistance, patient lifts hips to maintain a horizontal body position. Hold for approximately 10 s, rest for 5 s; 15 repetitions per set, 2 sets. The exercise difficulty was selected and adjusted in a timely manner based on the patient's condition, performance during training, and subjective feedback. |
Participants received group-specific interventions 5 days/week for 4 weeks.
Participants received group-specific interventions 5 days/week for 4 weeks.
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Co mierzy badanie?
Podstawowe miary wyniku
Podstawowe miary wyniku
Miara wyniku |
Opis środka |
Ramy czasowe |
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Functional near-infrared spectroscopy
Ramy czasowe: Baseline, 4-weeks treatment
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Near-infrared Brain Functional Imaging:The testing areas cover the bilateral prefrontal lobes, motor areas, occipital lobes, and other brain regions.
Within 1 week before treatment initiation, a physician will collect resting-state and task-state fNIRS data from enrolled patients.Resting-State Data Collection:The patient is fitted with an fNIRS measurement headcap.
In a quiet, comfortable environment, they are instructed to sit, relax, keep eyes closed (without falling asleep), and data are collected for 5 minutes.Task-State Data Collection:A walking paradigm is set up.
The test includes a 10-second preparatory phase where the patient stands at rest, followed by the task phase:Upon the command "Please start walking," the subject alternates stepping for 30 seconds.At the command "Stop," they cease walking and stand in place to rest for 30 seconds.
This "walk-rest" cycle is repeated 4 times.Identical data collection will be completed within 1 week after treatment concludes.
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Baseline, 4-weeks treatment
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Three-Dimensional Gait
Ramy czasowe: Baseline, 4-weeks treatment
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Gait spatiotemporal parameters - Lower limb joint angles - Lower limb joint moments - Ground reaction forces etc.
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Baseline, 4-weeks treatment
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Miary wyników drugorzędnych
Miary wyników drugorzędnych
Miara wyniku |
Opis środka |
Ramy czasowe |
|---|---|---|
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Ocena Fugl Meyer
Ramy czasowe: Linia bazowa, leczenie 4 tygodni
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Ocena FUGL-Meyer (FMA) służy do oceny funkcji motorycznej kończyny dolnej i koordynacji badań.
Zmodyfikowana z metody oceny Brunnstrom, ta skala jest podzielona na dwie części: ocenę funkcji kończyny górnej i dolnej kończyny, przy czym w tym badaniu zastosowano tylko podskala kończyn dolnej (FMA-LE).
FMA-LE składa się z 17 pozycji, z których każdy ocenił na trzy poziomy (0 punktów = niezdolny do wykonania; 1 punkt = częściowo wykonany; 2 punkty = w pełni wykonany), z całkowitym wynikiem od 0 do 34.
Wyższy wynik wskazuje na lepszą funkcję silnika kończyny dolnej.
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Linia bazowa, leczenie 4 tygodni
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Współpracownicy i badacze
Sponsor
Sponsor
Śledczy
Śledczy
- Krzesło do nauki: Xue Jiang, Shengjing Hospital
Daty zapisu na studia
Główne daty studiów
Rozpoczęcie studiów (Szacowany)
Rozpoczęcie studiów
Zakończenie podstawowe (Szacowany)
Zakończenie podstawowe
Ukończenie studiów (Szacowany)
Ukończenie studiów
Daty rejestracji na studia
Pierwszy przesłany
Pierwszy przesłany
Pierwszy przesłany, który spełnia kryteria kontroli jakości
Pierwszy przesłany, który spełnia kryteria kontroli jakości
Pierwszy wysłany (Rzeczywisty)
Pierwszy wysłany
Aktualizacje rekordów badań
Ostatnia wysłana aktualizacja (Rzeczywisty)
Ostatnia wysłana aktualizacja
Ostatnia przesłana aktualizacja, która spełniała kryteria kontroli jakości
Ostatnia przesłana aktualizacja, która spełniała kryteria kontroli jakości
Ostatnia weryfikacja
Ostatnia weryfikacja
Więcej informacji
Terminy związane z tym badaniem
Słowa kluczowe
Dodatkowe istotne warunki MeSH
Inne numery identyfikacyjne badania
Inne numery identyfikacyjne badania
- 2025PS1878K(X1)
Plan dla danych uczestnika indywidualnego (IPD)
Planujesz udostępniać dane poszczególnych uczestników (IPD)?
Opis planu IPD
Ramy czasowe udostępniania IPD
Informacje o lekach i urządzeniach, dokumenty badawcze
Bada produkt leczniczy regulowany przez amerykańską FDA
Bada produkt urządzenia regulowany przez amerykańską FDA
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