The Utility of Cerebellar Transcranial Magnetic Stimulation in the Neurorehabilitation of Dysphagia After Stroke
Primary Purpose
Oropharyngeal Dysphagia, Stroke
Status
Completed
Phase
Not Applicable
Locations
United Kingdom
Study Type
Interventional
Intervention
Cerebellar TMS
Sham cerebellar TMS
Sponsored by
About this trial
This is an interventional treatment trial for Oropharyngeal Dysphagia focused on measuring Oropharyngeal Dysphagia, Stroke
Eligibility Criteria
Inclusion Criteria:
- Patients aged 18 years and over
- All patients with an acute anterior or posterior cerebral circulation stroke within 6 weeks of symptom onset.
Exclusion Criteria:
- Advanced dementia
- Previous history of dysphagia
- Patients judged to be clinically unstable
- Presence of implanted cardiac pacemaker or defibrillator
- Any severe chronic medical condition that compromises cardiac or respiratory status
- Patients with acute lower respiratory tract infections requiring antibiotic treatment.
Sites / Locations
- Upper G.I laboratory, Salford Royal Hospital
- Stroke Unit, Nottingham University Hospitals
Arms of the Study
Arm 1
Arm 2
Arm 3
Arm 4
Arm 5
Arm Type
Active Comparator
Active Comparator
Sham Comparator
Active Comparator
Sham Comparator
Arm Label
Hypothesis 2 Protocol 2 Low dose TMS
Hypothesis 2 Protocol 2 High dose TMS
Hypothesis 2 Protocol 2 Sham
Hypothesis 2 Protocol 1 Cerebellar TMS
Hypothesis 2 Protocol 1 Sham
Arm Description
Low level cerebellar TMS. Delivered once per day for 3 days.
High level cerebellar TMS. Delivered twice per day for 5 days.
Sham cerebellar TMS. Delivered twice a day for 5 days.
Cerebellar TMS at 10Hz, 250 pulses.
Sham cerebellar TMS
Outcomes
Primary Outcome Measures
Penetration aspiration scores on videofluoroscopy (number of swallows out of 6 that score 3 or more on the penetration aspiration scale) (Hypothesis 2 protocols 1 and 2)
Penetration aspiration scores on videofluoroscopy (number of swallows out of 6 that score 3 or more on the penetration aspiration scale)
Secondary Outcome Measures
Improvement of: Functional oral ingestion scale (FOIS) and or the dysphagia severity rating scale (DSRS) (Hypothesis 2 protocol 2)
Improvement of: Functional oral ingestion scale (FOIS) and or the dysphagia severity rating scale (DSRS)
Full Information
NCT ID
NCT03274947
First Posted
August 14, 2017
Last Updated
November 30, 2022
Sponsor
University of Manchester
Collaborators
Medical Research Council, University of Nottingham
1. Study Identification
Unique Protocol Identification Number
NCT03274947
Brief Title
The Utility of Cerebellar Transcranial Magnetic Stimulation in the Neurorehabilitation of Dysphagia After Stroke
Official Title
An Exploration of the Application of Non-invasive Cerebellar Stimulation in the Neurorehabilitation of Dysphagia After Stroke
Study Type
Interventional
2. Study Status
Record Verification Date
November 2022
Overall Recruitment Status
Completed
Study Start Date
January 14, 2019 (Actual)
Primary Completion Date
June 30, 2022 (Actual)
Study Completion Date
October 31, 2022 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of Manchester
Collaborators
Medical Research Council, University of Nottingham
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Product Manufactured in and Exported from the U.S.
No
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
The study is designed to explore the effectiveness of non-invasive cerebellar stimulation to enhance motor plasticity in the cortex after stroke. The investigators have shown that the human cerebellum is strongly activated during the act of swallowing and when stimulated with single TMS pulses can strongly facilitate the corticobulbar projection to the pharynx in humans. More recently the investigators have identified the most relevant frequency of stimulation of the cerebellum that can produce longer term excitation in the human swallowing motor system. The investigators therefore believe that the potential for cerebellar stimulation in improving swallowing is much greater than other methods for two reasons. Firstly, previous work has shown that unlike successful recovery of hand/arm function which relies on restoring activity in the stroke hemisphere, recovery of swallowing function relies on increased excitability in intact projections from the non-stroke hemisphere. The investigators believe that methods that can enhance these undamaged pathways have a greater chance of inducing recovery in the human swallowing system in unilateral stroke. Additionally cerebellar stimulation produces very high levels of corticobulbar excitation it may also have the advantage of improving dysphagia in posterior fossa strokes. Second, the human cerebellum is relatively easy to target and stimulate and has reduced risk of inducing unwanted effects (such as seizures) which as a consequence makes cerebellar stimulation a more pragmatic method for delivering therapeutic neurorehabilitation to dysphagic stroke patients compared to other more complex/riskier methods.
A final factor is that the investigators have developed a "virtual lesion" model of swallowing dysfunction in healthy volunteers which can be reversed quite successfully with other neuro-stimulation protocols. The investigators can therefore use this model to test the effectiveness of cerebellar stimulation protocols (ipsilateral and contralateral cerebellar sites) before choosing the most effective side to apply stimulation in a proof of principle trial/study in a small group of sub-acute dysphagic patients.
The hypotheses are that cerebellar TMS will:
i. Reverse the brain inhibition and behavioural dysfunction following a virtual lesion model of disrupted swallowing in healthy brain (phase 1); ii. Reduce the degree of aspiration in acute dysphagia after a stroke (phase 2).
Detailed Description
Protocols:
Hypothesis 1:
Cortical excitability (in both dominant and non-dominant swallowing cortex) to TMS and swallowing behaviour assessed with a swallowing reaction time task will be measured at baseline. Thereafter, the virtual lesion paradigm will be applied to the dominant swallowing projection followed by the cerebellar intervention (10Hz, 250 pulses). Cerebellar stimulation will be applied (in a randomised fashion) on separate occasions to both the contralateral and ipsilateral cerebellar hemispheres, immediately after the virtual lesion. The investigators have found that placement using known reference landmarks are equivalent to using neuronavigation, so the latter will not be employed. Repeat measurements of cortical excitability and swallowing behaviour will then be performed and analysed against baseline data and a sham cerebellar paradigm. Differences in cortical excitability and swallowing responses will thus be an indication of which cerebellar region (contralesional/ipsilesional) can influence excitability and reverse any behavioural changes most effectively.
Hypothesis 2:
I. Dysphagic stroke patients (n=24) recruited over a 9 month period within 14 days of stroke ictus will have their swallowing assessed by videofluoroscopy before and after receiving either the real or sham cerebellar stimulation (10Hz, 250 pulses) as determined from phase 1. As before, placement of the coil for cerebellar stimulation will be performed using landmarks already established and validated in the work from question 1. Patients will be intubated with the pharyngeal EMG catheter for pre and post recordings of pharyngeal motor evoked potentials (MEPs) to cortical TMS. Power calculations, based on a similar study of pharyngeal stimulation indicated that the investigators would need 12 patients per group to achieve a statistical power of 80% at a 5% significance level to detect changes in the primary outcome measure of aspiration. In this study, the investigators will examine if the chosen site of cerebellar stimulation from phase 1 can induce short-term changes in brain function (pharyngeal MEPs) and swallowing function (videofluoroscopy) compared to sham interventions and baseline measurement, up to 1 hour after the intervention.
II. Following stage I, once it is established that cerebellar stimulation can alter brain and swallowing functions in stroke in the short-term, it will need to be appraised for clinical feasibility, dose response, and longer term efficacy. Dysphagic stroke patients (n=48, 16 patients per group) admitted to the stroke unit and identified by videofluoroscopy will be recruited over the next 21 months. Since it is not known how the cerebellar stimulation method should be delivered to patients, a dose ranging treatment trial will be utilised, randomising patients to one of three groups (A-C), low level stimulation, high level stimulation and sham stimulation. From our previous work with pharyngeal stimulation, the investigators propose that group A will receive stimulation once per day for 3 days. Group B will receive stimulation twice per day for 5 days. Group C will receive sham stimulation (delivered as in protocol I) twice a day for 5 days. Groups A and B will receive stimulation at the optimal site (10Hz, 250 pulses) found in question 1, but all groups will also receive standard speech and language therapy.
Assessments:
Swallowing before and after stimulation will be evaluated using videofluoroscopy, at 1 hour for protocol I. For protocol II the investigators propose both videofluoroscopy and functional scores (Functional oral ingestion scale (FOIS), the dysphagia severity rating scale (DSRS) including feeding status and modified rankin scale (mRS)) at baseline and at 2 weeks.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Oropharyngeal Dysphagia, Stroke
Keywords
Oropharyngeal Dysphagia, Stroke
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Participant
Allocation
Randomized
Enrollment
15 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Hypothesis 2 Protocol 2 Low dose TMS
Arm Type
Active Comparator
Arm Description
Low level cerebellar TMS. Delivered once per day for 3 days.
Arm Title
Hypothesis 2 Protocol 2 High dose TMS
Arm Type
Active Comparator
Arm Description
High level cerebellar TMS. Delivered twice per day for 5 days.
Arm Title
Hypothesis 2 Protocol 2 Sham
Arm Type
Sham Comparator
Arm Description
Sham cerebellar TMS. Delivered twice a day for 5 days.
Arm Title
Hypothesis 2 Protocol 1 Cerebellar TMS
Arm Type
Active Comparator
Arm Description
Cerebellar TMS at 10Hz, 250 pulses.
Arm Title
Hypothesis 2 Protocol 1 Sham
Arm Type
Sham Comparator
Arm Description
Sham cerebellar TMS
Intervention Type
Device
Intervention Name(s)
Cerebellar TMS
Intervention Description
Cerebellar transcranial magnetic stimulation
Intervention Type
Device
Intervention Name(s)
Sham cerebellar TMS
Intervention Description
Sham cerebellar transcranial magnetic stimulation
Primary Outcome Measure Information:
Title
Penetration aspiration scores on videofluoroscopy (number of swallows out of 6 that score 3 or more on the penetration aspiration scale) (Hypothesis 2 protocols 1 and 2)
Description
Penetration aspiration scores on videofluoroscopy (number of swallows out of 6 that score 3 or more on the penetration aspiration scale)
Time Frame
1 hour post intervention and 2 weeks post intervention
Secondary Outcome Measure Information:
Title
Improvement of: Functional oral ingestion scale (FOIS) and or the dysphagia severity rating scale (DSRS) (Hypothesis 2 protocol 2)
Description
Improvement of: Functional oral ingestion scale (FOIS) and or the dysphagia severity rating scale (DSRS)
Time Frame
2 weeks post intervention
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria:
Patients aged 18 years and over
All patients with an acute anterior or posterior cerebral circulation stroke within 6 weeks of symptom onset.
Exclusion Criteria:
Advanced dementia
Previous history of dysphagia
Patients judged to be clinically unstable
Presence of implanted cardiac pacemaker or defibrillator
Any severe chronic medical condition that compromises cardiac or respiratory status
Patients with acute lower respiratory tract infections requiring antibiotic treatment.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Shaheen Hamdy, MBChB, PhD
Organizational Affiliation
University of Manchester
Official's Role
Principal Investigator
Facility Information:
Facility Name
Upper G.I laboratory, Salford Royal Hospital
City
Manchester
State/Province
Greater Manchester
ZIP/Postal Code
M6 8HD
Country
United Kingdom
Facility Name
Stroke Unit, Nottingham University Hospitals
City
Nottingham
State/Province
Notthinghamshire
Country
United Kingdom
12. IPD Sharing Statement
Plan to Share IPD
No
IPD Sharing Plan Description
No identifiable individual participant information will be shared outside the immediate research team. However, identifiable individual participant information will be made available to the Medical research council and the University of Manchester if required for the purposes of auditing the study.
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The Utility of Cerebellar Transcranial Magnetic Stimulation in the Neurorehabilitation of Dysphagia After Stroke
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