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Augmented Efficacy of rPMS on the rTMS on Upper Limb Function in Patients With Stroke

16 agosto 2022 aggiornato da: Chang Gung Memorial Hospital

Augmented Efficacy of Repetitive Peripheral Magnetic Stimulation on the Repetitive Transcranial Magnetic Stimulation on Upper Limb Function in Patients With Stroke: a Randomized Controlled Trial

Repetitive transcranial magnetic stimulation (rTMS) and repetitive peripheral magnetic stimulation (rPMS) are innovative treatments for patients with stroke. Therefore, augmented efficacy of rPMS on the rTMS is employed in this project. This proposal aims at exploring different novel treatment strategies in the treatment of UE dysfunction in patients with stroke: augmented efficacy of rPMS on the rTMS. Several aims in this study include (1) identifying the most optimal treatment protocols for rPMS (TBS treatment and nerve stimulation location), (2 ) establish a novel treatment protocol (augmented efficacy of rPMS on the rTMS), (3) identifying augmented efficacy of rPMS on the rTMS, (4) determining the mechanism of neuro-motor control, and (5) related biomarkers for the novel treatment protocol. The investigators applied a 3-year plan before, however, the Ministry of Science and Technology plan passed one year only (108-2314-B-182-043-). The investigators carried out the pilot study to investigate the augmented effects of rPMS (radial nerve) on the rTMS in the treatment of upper limb function in patients with stroke patients. The previous plan had preliminary results. This year the investigators will apply for a three-year plan to continue the previous pilot study for getting the comprehensive results.

Panoramica dello studio

Stato

Reclutamento

Condizioni

Intervento / Trattamento

Descrizione dettagliata

This study intends to further explore whether rPMS intervention in different nerves can augment rTMS efficacy on upper limb function in patients with stroke. A total of 72-96 patients with stroke will be recruited in 2 phases and 36-48 participants will be divided into four groups according to their severity and the onset of stroke, and then randomly enrolled into 3 groups in each phase (12-16 participants in each group) based on different rPMS- stimulated methods and location. All patients will receive the rPMS in addition rTMS on the brain cortex. In phase 1, each patient will receive either one of three rPMS methods on median nerve (iTBS, cTBS, sham). During phase 2, each patient will receive either one of three rPMS methods on ulnar nerve. Outcome measures include clinical assessments based on International Classification of Functioning, Disability and Health (ICF) and motor control (Motor Evoked Potential, MEP, kinetics, and kinematics) that administered at pretest, posttest, and 3-month follow-up. This study aims to establish a novel assessment and treatment protocols in patients with stroke. The intervention will be conducted 10 times for each participant. The optimal effective treatment protocol of augmented efficacy of rPMS on the rTMS will also be established. The results of this study will be applied to the translational and evidence-based medicine of the neuro-rehabilitation field of stroke research.

Tipo di studio

Interventistico

Iscrizione (Anticipato)

96

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.

Luoghi di studio

  • Taiwan
      • Taoyuan, Taiwan
        • Reclutamento
        • Chang Gung Memoria Hospital

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

Da 20 anni a 80 anni (Adulto, Adulto più anziano)

Accetta volontari sani

No

Sessi ammissibili allo studio

Tutto

Descrizione

Inclusion Criteria:

  • first stoke and in stable phase
  • age 20-80 years
  • unilateral brain lesions with unilateral hemiplegia
  • brain wave examination without epileptic waves

Exclusion Criteria:

  • brain stem or cerebellar stroke
  • Patients with epilepsy
  • Patients with aneurysm or cerebrovascular malformation
  • Patients with mental illness
  • Patients with degenerative diseases (such as neurodegenerative diseases)
  • Patients with severe intelligence or language barriers (such as mental retardation or severe communication impairment)
  • Patients with serious medical conditions (such as heart failure)
  • Patients with acute disease (such as infection)
  • Patients had metal implants in the body (such as cardiac rhythm or brain metal implants, metal clips for aneurysms)
  • Patients had botox injection or surgery in the first half of the study
  • Pregnant woman or breastfeeding woman
  • other obstacles (such as claustrophobia, obesity, etc.)

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 incrociata
  • Mascheramento: Doppio

Armi e interventi

Gruppo di partecipanti / Arm
Intervento / Trattamento
Sperimentale: rTMS+rPMS_iTBS_M
In this group, they received iTBS on affected hemisphere after following iTBS at median nerve on affected hand.
Dispositivo: rTMS+rPMS_iTBS_M
Repetitive peripheral magnetic stimulation (rPMS) intermittent theta-burst stimulation pattern (iTBS) will intermittently give a 2 s train of iTBS every 10s repeated 2 times for a total of 40 times at median nerve on the affected hand(low pulse: 1200 pulses in total). Then following Repetitive transcranial magnetic stimulation (rTMS) will intermittently give a 2 s train of iTBS every 10s repeated 2 times for a total of 40 times on affected hemisphere(low pulse: 1200 pulses in total).
Sperimentale: rTMS+rPMS_cTBS_M
In this group, they received iTBS on affected hemisphere after following cTBS at median nerve on affected hand.
Dispositivo: rTMS+rPMS_cTBS_M
Repetitive peripheral magnetic stimulation (rPMS) continuous burst stimulation pattern (cTBS) will intermittently give a cTBS treatment consists of a continuous train of TBS for 40 seconds repeated for 2 times at median nerve on the affected hand(low pulse: 1200 pulses in total). Then following Repetitive transcranial magnetic stimulation (rTMS) will intermittently give a 2 s train of iTBS every 10s repeated 2 times for a total of 40 times on affected hemisphere(low pulse: 1200 pulses in total).
Comparatore fittizio: rTMS+sham rPMS_M
In this group, they received iTBS on affected hemisphere after following sham TBS stimulation at median nerve on affected hand.
Dispositivo: rTMS+sham rPMS_M
Repetitive peripheral magnetic stimulation (rPMS) sham burst stimulation pattern (sham TBS) will intermittently give a sham TBS treatment consists of a continuous train of TBS for 40 seconds at median nerve on the affected hand(almost no pulse: 1200 pulses in total). Then following Repetitive transcranial magnetic stimulation (rTMS) will intermittently give a sham TBS treatment consists of a continuous train of TBS for 40 seconds on affected hemisphere(almost no pulse: 1200 pulses in total).
Sperimentale: rTMS+rPMS_iTBS_U
In this group, they received iTBS on affected hemisphere after following iTBS at ulnar nerve on affected hand.
Dispositivo: rTMS+rPMS_iTBS_U
Repetitive peripheral magnetic stimulation (rPMS) intermittent theta-burst stimulation pattern (iTBS) will intermittently give a 2 s train of iTBS every 10s repeated 2 times for a total of 40 times at ulnaris nerve on the affected hand(low pulse: 1200 pulses in total). Then following Repetitive transcranial magnetic stimulation (rTMS) will intermittently give a 2 s train of iTBS every 10s repeated 2 times for a total of 40 times on affected hemisphere(low pulse: 1200 pulses in total).
Sperimentale: rTMS+rPMS_cTBS_U
In this group, they received iTBS on affected hemisphere after following cTBS at ulnar nerve on affected hand.
Dispositivo: rTMS+rPMS_cTBS_U
Repetitive peripheral magnetic stimulation (rPMS) continuous burst stimulation pattern (cTBS) will intermittently give a cTBS treatment consists of a continuous train of TBS for 40 seconds repeated for 2 times at ulnar nerve on the affected hand(low pulse: 1200 pulses in total). Then following Repetitive transcranial magnetic stimulation (rTMS) will intermittently give a 2 s train of iTBS every 10s repeated 2 times for a total of 40 times on affected hemisphere(low pulse: 1200 pulses in total).
Comparatore fittizio: rTMS+sham rPMS_U
In this group, they received iTBS on affected hemisphere after following sham TBS stimulation at ulnar nerve on affected hand.
Dispositivo: rTMS+sham rPMS_U
Repetitive peripheral magnetic stimulation (rPMS) sham burst stimulation pattern (sham TBS) will intermittently give a sham TBS treatment consists of a continuous train of TBS for 40 seconds at ulnar nerve on the affected hand(almost no pulse: 1200 pulses in total). Then following Repetitive transcranial magnetic stimulation (rTMS) will intermittently give a sham TBS treatment consists of a continuous train of TBS for 40 seconds on affected hemisphere(almost no pulse: 1200 pulses in total).

Cosa sta misurando lo studio?

Misure di risultato primarie

Misura del risultato
Misura Descrizione
Lasso di tempo
Change from baseline Motion analysis at after treatment and three month
Lasso di tempo: baseline, after two weeks of treatment, 3 months
All participants will be instructed to perform a series of upper-extremity tasks. The tasks include reaching and grasping. An 7-camera motion analysis system (Vicon system, 3-D Oxfort Metrics Ltd, Oxford, UK) is used in conjunction with a personal computer to capture the movement of markers placed on the participant's body; analog signals were collected simultaneously. Movements were recorded at 120 Hz and digitally low-pass filtered at 5 Hz using a second-order Butterworth filter. Reference markers are placed on the distal interphalangeal joints of the thumb and index finger, the styloid process of the ulna, proximal end of the second metacarpal, and the object.
baseline, after two weeks of treatment, 3 months
Change from baseline Motor evoked potential at afte treatment and three month
Lasso di tempo: baseline, after two weeks of treatment, 3 months
The comparison of baseline of Motor Evoked Potential for stroke after different therapy, including resting motor threshold (RMT), active motor thresholds (AMT), input-output curve (IO curve) and stationary period.
baseline, after two weeks of treatment, 3 months
Change from baseline Myoton at after treatment and three month
Lasso di tempo: baseline, after two weeks of treatment, 3 months
The comparison of baseline of Myoton for stroke after different therapy, assessing the functional status of skeletal muscle, including tone or state of tension(natural oscillation frequency[Hz]), biochanical properties(dynamic stiffness [N/m], logarithmic decrement of natural oscillation), viscoelastic properties(mechanical stress relaxation time [ms], ratio of deformation and relaxation time, characterising Creep (Deborah number)).
baseline, after two weeks of treatment, 3 months
Change from baseline Muscle strength at after treatment and three month
Lasso di tempo: baseline, after two weeks of treatment, 3 months
The comparison of baseline of Muscle strength for stroke after different therapy, including lateral pinch, palmar pinch, and tip pinch, the strength will be tested by hand dynamometer.
baseline, after two weeks of treatment, 3 months
Change from baseline Brunnstrom stage at after treatment and three month
Lasso di tempo: baseline, after two weeks of treatment, 3 months
The Brunnstrom stage is used to classify the severity of stroke patient according to specific movement.
baseline, after two weeks of treatment, 3 months
Change from baseline Fugl Meyer Assessment at after treatment and three month
Lasso di tempo: baseline, after two weeks of treatment, 3 months
The Fugl Meyer Assessment is used to measure upper and lower extremity motor , range of motion, sensation, pain and balance.
baseline, after two weeks of treatment, 3 months
Change from baseline Modified Ashworth Scale at after treatment and three month
Lasso di tempo: baseline, after two weeks of treatment, 3 months
The Modified Ashworth Scale is used to measure the muscle tone of affected limb, for each item minimum value is 0 and maximum value is 4, higher scores mean a worse outcome.
baseline, after two weeks of treatment, 3 months

Misure di risultato secondarie

Misura del risultato
Misura Descrizione
Lasso di tempo
Change from baseline Action Research Arm Test at after treatment and three month
Lasso di tempo: baseline, after two weeks of treatment, 3 months
The Action Research Arm Test is used to measure bilateral gross manual and finger dexterity.
baseline, after two weeks of treatment, 3 months
Change from baseline Box and Block Test at after treatment and three month
Lasso di tempo: baseline, after two weeks of treatment, 3 months
The Box and Block Test (BBT) measures unilateral gross manual dexterity.
baseline, after two weeks of treatment, 3 months
Change from baseline Nine-Hole test at after treatment and three month
Lasso di tempo: baseline, after two weeks of treatment, 3 months
The Nine-Hole Peg Test (NHPT) is used to measure finger dexterity in patients with various neurological diagnoses.
baseline, after two weeks of treatment, 3 months
Change from baseline Jebson Taylor Hand Function Test at after treatment and three month
Lasso di tempo: baseline, after two weeks of treatment, 3 months
The Jebson Taylor Hand Function Test (JTHFT) is used to assess a broad range of unilateral hand functions required for activities of daily living(ADLs).
baseline, after two weeks of treatment, 3 months
Change from baseline Functional Independence Measure at after treatment and three month
Lasso di tempo: baseline, after two weeks of treatment, 3 months
The purpose of Functional Independence Measure(FIM) is to understand and track adult's life function performance, progress and goal achievement. There are three main areas: self-care, mobility, and cognition. The score is from 1 to 7 points, 1 is completely dependent, and 7 is completely independent.
baseline, after two weeks of treatment, 3 months
Change from baseline Motor Activity Log at after treatment and three month
Lasso di tempo: baseline, after two weeks of treatment, 3 months
The Motor Activity Log(MAL) is used to measure the quality and quantity of a stroke patient when performing activities using the affected hand.
baseline, after two weeks of treatment, 3 months
Change from baseline Wolf Motor Function Test at after treatment and three month
Lasso di tempo: baseline, after two weeks of treatment, 3 months
The Wolf Motor Function Test(WMFT) is used to measure unilateral motor quality and strength.
baseline, after two weeks of treatment, 3 months
Change from baseline Nottingham Health Profile at after treatment and three month
Lasso di tempo: baseline, after two weeks of treatment, 3 months
The Nottingham Health Profile(NHP) is a questionnaire that assesses the quality of life associated with health. There are a total of 38 items, divided into six sub-items: mobility, social isolation, emotional response, pain, sleep and energy.
baseline, after two weeks of treatment, 3 months
Change from baseline Stroke Impact Scale at after treatment and three month
Lasso di tempo: baseline, after two weeks of treatment, 3 months
The Stroke Impact Scale(SIS) is used to measure the influence of several aspects after stroke, for each item minimum value is 1 and maximum value is 5, higher scores mean a better outcome.
baseline, after two weeks of treatment, 3 months

Collaboratori e investigatori

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

Sponsor

Chang Gung Memorial Hospital

Collaboratori

Ministry of Science and Technology, Taiwan

Investigatori

  • Direttore dello studio: Chia-Ling Chen, Chang Gung Memorial Hospital

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 (Effettivo)

1 agosto 2021

Completamento primario (Anticipato)

1 settembre 2024

Completamento dello studio (Anticipato)

1 settembre 2024

Date di iscrizione allo studio

Primo inviato

3 settembre 2021

Primo inviato che soddisfa i criteri di controllo qualità

13 settembre 2021

Primo Inserito (Effettivo)

22 settembre 2021

Aggiornamenti dei record di studio

Ultimo aggiornamento pubblicato (Effettivo)

17 agosto 2022

Ultimo aggiornamento inviato che soddisfa i criteri QC

16 agosto 2022

Ultimo verificato

1 agosto 2021

Maggiori informazioni

Termini relativi a questo studio

Parole chiave

Termini MeSH pertinenti aggiuntivi

Altri numeri di identificazione dello studio

  • 202002582A3

Piano per i dati dei singoli partecipanti (IPD)

Hai intenzione di condividere i dati dei singoli partecipanti (IPD)?

NO

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 .

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