Deglutition Disorders Clinical Trial
Official title:
The Effectiveness of Repetitive Transcranial Magnetic Stimulation (rTMS) in Patients With Chronic Poststroke Dysphagia.
The goal of this study is to investigate the therapeutic efficacy of repetitive transcranial magnetic stimulation (rTMS) and intermittent theta burst stimulation (iTBS) applying on suprahyoid motor cortex in chronic poststroke dysphagia, and its effect on hyolaryngeal movement. Participants will be randomized into three groups. The three experimental groups received either bilateral or ipsilateral rTMS, or iTBS (with contralateral sham stimulation) at suprahyoid motor cortex, while the placebo group received bilateral sham stimulation. Stimulation will be given at 5 hertz(Hz), 1000 pulses of rTMS or 600 pulses of iTBS per session, for a total of 10 sessions. The swallowing function, penetration-aspiration scale of video-fluoroscopic swallowing study, motor evoked potential of suprahyoid muscles, intraoral pressure, and ultrasound swallowing exam will be evaluated before therapy, and at 1, 3, 6 months post therapy.
Status | Not yet recruiting |
Enrollment | 150 |
Est. completion date | August 31, 2024 |
Est. primary completion date | May 1, 2024 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 20 Years and older |
Eligibility | Inclusion Criteria: - age > 20 years old, diagnosed of subcortical stroke(including ischemic or hemorrhagic type) by CT or MRI image study - sustained the symptoms of dysphagia more than one month after stroke. - Functional Oral Intake Scale (FOIS) between 1 to 5 score - Maintenance on sitting balance over 15 minutes Exclusion Criteria: - Disturbed consciousness, unable to communicate and obey order through gesture or language - Disease or trauma involved central neural system, such as Parkinson's disease, traumatic brain injury, brain tumor or multiple sclerosis - Any disorder inducing dysphagia, such as nasopharyngeal cancer(NPC) or cervical cancer - Metal Implants or pacemaker - Global aphasia or cognitive impairment - History of epilepsy - Pregnancy |
Country | Name | City | State |
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n/a |
Lead Sponsor | Collaborator |
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National Taiwan University Hospital |
Rao J, Li F, Zhong L, Wang J, Peng Y, Liu H, Wang P, Xu J. Bilateral Cerebellar Intermittent Theta Burst Stimulation Combined With Swallowing Speech Therapy for Dysphagia After Stroke: A Randomized, Double-Blind, Sham-Controlled, Clinical Trial. Neurorehabil Neural Repair. 2022 Jul;36(7):437-448. doi: 10.1177/15459683221092995. Epub 2022 May 16. — View Citation
Rossi S, Hallett M, Rossini PM, Pascual-Leone A; Safety of TMS Consensus Group. Safety, ethical considerations, and application guidelines for the use of transcranial magnetic stimulation in clinical practice and research. Clin Neurophysiol. 2009 Dec;120(12):2008-2039. doi: 10.1016/j.clinph.2009.08.016. Epub 2009 Oct 14. — View Citation
Wen X, Liu Z, Zhong L, Peng Y, Wang J, Liu H, Gong X. The Effectiveness of Repetitive Transcranial Magnetic Stimulation for Post-stroke Dysphagia: A Systematic Review and Meta-Analysis. Front Hum Neurosci. 2022 Mar 17;16:841781. doi: 10.3389/fnhum.2022.841781. eCollection 2022. — View Citation
Yu-Lei X, Shan W, Ju Y, Yu-Han X, Wu Q, Yin-Xu W. Theta burst stimulation versus high-frequency repetitive transcranial magnetic stimulation for poststroke dysphagia: A randomized, double-blind, controlled trial. Medicine (Baltimore). 2022 Jan 14;101(2):e28576. doi: 10.1097/MD.0000000000028576. — View Citation
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | penetration-aspiration scale(PAS) | Penetration-aspiration scale will be calculated by videofluoroscopic swallow study with measurement of the depth of penetrated or aspirated material and the patient's response to airway invasion. Score range is 1 to 8; higher score means more severe on penetration and aspiration. | Day 30 (change of PAS, comparing with the data in baseline) of each section | |
Primary | penetration-aspiration scale(PAS) | Penetration-aspiration scale will be calculated by videofluoroscopic swallow study with measurement of the depth of penetrated or aspirated material and the patient's response to airway invasion. Score range is 1 to 8; higher score means more severe on penetration and aspiration. | Day 90 (change of PAS, comparing with the data in baseline and Day 30) of each section | |
Secondary | The Swallowing Quality-of-Life questionnaire(SWAL-QOL) | The questionnaire to assess ten quality-of-life concepts about dysphagia, containing 44-items and dividing into 10 domains. The score of each item ranges from 0 to 4 and total score ranges from 0 to 100. Higher score means better swallow-specific quality of life. | Day 14, Day 30, Day 90, Day 180 (comparing with the data in baseline) of each section | |
Secondary | The Functional Oral Intake Scale (FOIS) | Measurement of functional level of oral intake of food and liquid with 7-point ordinal scale, level 1 to level 7. Higher level means better performance and lower limitation on oral intake. | Day 14, Day 30, Day 90, Day 180 (comparing with the data in baseline) of each section | |
Secondary | The Dysphagia Severity Scale (DSS) | Combination of objective evaluation of the functional severity of dysphagia and recommendations for diet level. Level range is from 1 to 7; lower level means more severe on dysphagia and aspiration. | Day 14, Day 30, Day 90, Day 180 (comparing with the data in baseline) of each section | |
Secondary | Iowa Oral Performance Instrument (IOPI) | Objectively evaluate and measure tongue and lip strength and endurance | Baseline, Day 14, Day 30, Day 90, Day 180 | |
Secondary | Swallowing ultrasound | The ultrasound of swallowing to evaluate the movement of hyoid bone | Baseline, Day 14, Day 30, Day 90, Day 180 | |
Secondary | Motor evoked potential (MEP) | Record the MEP of suprahyoid muscle under rTMS | Baseline, Day 14 |
Status | Clinical Trial | Phase | |
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Not yet recruiting |
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