Augmented Efficacy of rPMS on the rTMS on Upper Limb Function in Patients With Stroke
16 augustus 2022 bijgewerkt door: 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.
Studie Overzicht
Toestand
Werving
Conditie
Gedetailleerde beschrijving
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.
Studietype
Ingrijpend
Inschrijving (Verwacht)
96
Fase
- Niet toepasbaar
Contacten en locaties
In dit gedeelte vindt u de contactgegevens van degenen die het onderzoek uitvoeren en informatie over waar dit onderzoek wordt uitgevoerd.
Studie Locaties
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Taoyuan, Taiwan
- Werving
- Chang Gung Memoria Hospital
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Deelname Criteria
Onderzoekers zoeken naar mensen die aan een bepaalde beschrijving voldoen, de zogenaamde geschiktheidscriteria. Enkele voorbeelden van deze criteria zijn iemands algemene gezondheidstoestand of eerdere behandelingen.
Geschiktheidscriteria
Leeftijden die in aanmerking komen voor studie
20 jaar tot 80 jaar (Volwassen, Oudere volwassene)
Accepteert gezonde vrijwilligers
Nee
Geslachten die in aanmerking komen voor studie
Allemaal
Beschrijving
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.)
Studie plan
Dit gedeelte bevat details van het studieplan, inclusief hoe de studie is opgezet en wat de studie meet.
Hoe is de studie opgezet?
Ontwerpdetails
- Primair doel: Behandeling
- Toewijzing: Gerandomiseerd
- Interventioneel model: Crossover-opdracht
- Masker: Dubbele
Wapens en interventies
Deelnemersgroep / Arm |
Interventie / Behandeling |
|---|---|
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Experimenteel: rTMS+rPMS_iTBS_M
In this group, they received iTBS on affected hemisphere after following iTBS at median nerve on affected hand.
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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).
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Experimenteel: rTMS+rPMS_cTBS_M
In this group, they received iTBS on affected hemisphere after following cTBS at median nerve on affected hand.
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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).
|
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Sham-vergelijker: rTMS+sham rPMS_M
In this group, they received iTBS on affected hemisphere after following sham TBS stimulation at median nerve on affected hand.
|
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).
|
|
Experimenteel: rTMS+rPMS_iTBS_U
In this group, they received iTBS on affected hemisphere after following iTBS at ulnar nerve on affected hand.
|
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).
|
|
Experimenteel: rTMS+rPMS_cTBS_U
In this group, they received iTBS on affected hemisphere after following cTBS at ulnar nerve on affected hand.
|
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).
|
|
Sham-vergelijker: rTMS+sham rPMS_U
In this group, they received iTBS on affected hemisphere after following sham TBS stimulation at ulnar nerve on affected hand.
|
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).
|
Wat meet het onderzoek?
Primaire uitkomstmaten
Uitkomstmaat |
Maatregel Beschrijving |
Tijdsspanne |
|---|---|---|
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Change from baseline Motion analysis at after treatment and three month
Tijdsspanne: baseline, after two weeks of treatment, 3 months
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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.
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baseline, after two weeks of treatment, 3 months
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Change from baseline Motor evoked potential at afte treatment and three month
Tijdsspanne: baseline, after two weeks of treatment, 3 months
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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.
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baseline, after two weeks of treatment, 3 months
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Change from baseline Myoton at after treatment and three month
Tijdsspanne: baseline, after two weeks of treatment, 3 months
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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)).
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baseline, after two weeks of treatment, 3 months
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Change from baseline Muscle strength at after treatment and three month
Tijdsspanne: baseline, after two weeks of treatment, 3 months
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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.
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baseline, after two weeks of treatment, 3 months
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Change from baseline Brunnstrom stage at after treatment and three month
Tijdsspanne: baseline, after two weeks of treatment, 3 months
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The Brunnstrom stage is used to classify the severity of stroke patient according to specific movement.
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baseline, after two weeks of treatment, 3 months
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Change from baseline Fugl Meyer Assessment at after treatment and three month
Tijdsspanne: baseline, after two weeks of treatment, 3 months
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The Fugl Meyer Assessment is used to measure upper and lower extremity motor , range of motion, sensation, pain and balance.
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baseline, after two weeks of treatment, 3 months
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Change from baseline Modified Ashworth Scale at after treatment and three month
Tijdsspanne: baseline, after two weeks of treatment, 3 months
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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.
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baseline, after two weeks of treatment, 3 months
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Secundaire uitkomstmaten
Uitkomstmaat |
Maatregel Beschrijving |
Tijdsspanne |
|---|---|---|
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Change from baseline Action Research Arm Test at after treatment and three month
Tijdsspanne: baseline, after two weeks of treatment, 3 months
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The Action Research Arm Test is used to measure bilateral gross manual and finger dexterity.
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baseline, after two weeks of treatment, 3 months
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Change from baseline Box and Block Test at after treatment and three month
Tijdsspanne: baseline, after two weeks of treatment, 3 months
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The Box and Block Test (BBT) measures unilateral gross manual dexterity.
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baseline, after two weeks of treatment, 3 months
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Change from baseline Nine-Hole test at after treatment and three month
Tijdsspanne: baseline, after two weeks of treatment, 3 months
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The Nine-Hole Peg Test (NHPT) is used to measure finger dexterity in patients with various neurological diagnoses.
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baseline, after two weeks of treatment, 3 months
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Change from baseline Jebson Taylor Hand Function Test at after treatment and three month
Tijdsspanne: baseline, after two weeks of treatment, 3 months
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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).
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baseline, after two weeks of treatment, 3 months
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Change from baseline Functional Independence Measure at after treatment and three month
Tijdsspanne: baseline, after two weeks of treatment, 3 months
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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.
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baseline, after two weeks of treatment, 3 months
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Change from baseline Motor Activity Log at after treatment and three month
Tijdsspanne: baseline, after two weeks of treatment, 3 months
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The Motor Activity Log(MAL) is used to measure the quality and quantity of a stroke patient when performing activities using the affected hand.
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baseline, after two weeks of treatment, 3 months
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Change from baseline Wolf Motor Function Test at after treatment and three month
Tijdsspanne: baseline, after two weeks of treatment, 3 months
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The Wolf Motor Function Test(WMFT) is used to measure unilateral motor quality and strength.
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baseline, after two weeks of treatment, 3 months
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Change from baseline Nottingham Health Profile at after treatment and three month
Tijdsspanne: baseline, after two weeks of treatment, 3 months
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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.
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baseline, after two weeks of treatment, 3 months
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Change from baseline Stroke Impact Scale at after treatment and three month
Tijdsspanne: baseline, after two weeks of treatment, 3 months
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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.
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baseline, after two weeks of treatment, 3 months
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Medewerkers en onderzoekers
Hier vindt u mensen en organisaties die betrokken zijn bij dit onderzoek.
Sponsor
Medewerkers
Onderzoekers
- Studie directeur: Chia-Ling Chen, Chang Gung Memorial Hospital
Studie record data
Deze datums volgen de voortgang van het onderzoeksdossier en de samenvatting van de ingediende resultaten bij ClinicalTrials.gov. Studieverslagen en gerapporteerde resultaten worden beoordeeld door de National Library of Medicine (NLM) om er zeker van te zijn dat ze voldoen aan specifieke kwaliteitscontrolenormen voordat ze op de openbare website worden geplaatst.
Bestudeer belangrijke data
Studie start (Werkelijk)
1 augustus 2021
Primaire voltooiing (Verwacht)
1 september 2024
Studie voltooiing (Verwacht)
1 september 2024
Studieregistratiedata
Eerst ingediend
3 september 2021
Eerst ingediend dat voldeed aan de QC-criteria
13 september 2021
Eerst geplaatst (Werkelijk)
22 september 2021
Updates van studierecords
Laatste update geplaatst (Werkelijk)
17 augustus 2022
Laatste update ingediend die voldeed aan QC-criteria
16 augustus 2022
Laatst geverifieerd
1 augustus 2021
Meer informatie
Termen gerelateerd aan deze studie
Trefwoorden
Aanvullende relevante MeSH-voorwaarden
Andere studie-ID-nummers
- 202002582A3
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Bestudeert een door de Amerikaanse FDA gereguleerd geneesmiddel
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Bestudeert een door de Amerikaanse FDA gereguleerd apparaatproduct
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