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Brief Summary
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INTRODUCTION
As
a fatal disease, stroke is currently the second most common cause of
disability. Movement problems of the limbs are among the many functional
deficits that frequently follow a stroke. The major symptoms are increased
muscular tone, decreased muscle strength, or aberrant movement patterns. These
can have a serious impact on the quality of life for patients and their
families, as well as heavily burden society. Five Clumsiness, slowness of
movement, or loss of limb movement are the symptoms of the patient’s damaged
side muscle. The normal function of a healthy limb may also be impacted by the
decreased bilateral limb synergy. Relying too much on the healthy upper limb
might result in secondary injuries from overusing the healthy limb or in the
affected limb becoming inactive The treatment of upper limb motor dysfunction
has expanded in recent years, with new approaches including neuromodulation,
acupuncture, rehabilitation training, and other therapies. [2]
About 50–80% of people with stroke experience
upper limb disability during the acute phase, and 40–50% during the chronic
phase.[6].
Following
a stroke, it is common to see both physical and cognitive problems.
Specifically, lower and upper limb motor impairments are linked to global
cognition, executive dysfunction, and memory impairment. Depending on factors
such as stroke type (ischemic or hemorrhagic), pre-stroke dementia, and
temporal distance from the acute event, the prevalence of post-stroke
neurocognitive problems varies from 7 to 67.3%.[6]
In
the world today, stroke continues to rank among the principal causes of death
and adult-onset disability. Despite physiotherapy and rehabilitation, a
considerable fraction of people who survive chronic stroke retain long-term
disability. Neurological deficiencies encompass a range of symptoms such as
spasticity, loss of coordination, dysphasia, weakness, visual field
dysfunction, and cognitive impairment. Beyond immediate expenditures like
medical bills, the broader socioeconomic effects of stroke include indirect
costs like missed productivity at work and the strain of caring for a loved
one. Neuroprotective drugs for acute stroke and innovative treatment approaches
that encourage neuroplasticity for chronic stroke are therefore unmet needs. [5]
Eighty
percent of the vagus nerve’s fibers are afferent, while just twenty percent are
efferent. It is vital to the preservation of autonomic tone. everywhere in the
abdomen, thorax, and brain [3]
One
such focused approach supports the recovery of upper limb function following a
chronic stroke by enhancing plasticity and utilizing short bursts of Vagus
Nerve Stimulation (VNS) in conjunction with rehabilitation. Acetylcholine and
norepinephrine, two neuromodulators that promote plasticity throughout the
cortex, are released when the vagus nerve is stimulated. When neuromodulators
are timed to fire in tandem with motor training, the motor cortex experiences
task-specific plasticity that enhances function and serves as the foundation
for paired vector neurostimulation therapy. Compared to rehabilitative training
without VNS, a number of studies using preclinical models of ischemic stroke
showed that VNS in combination with training greatly enhanced the recovery of
forelimb motor function Improvements were linked to remaining motor neurons
controlling the damaged forelimb being recruited and cortical motor networks
being reorganized synaptic ally, indicating potential neurobiological pathways
driving motor function recovery.[9]
Transcutaneous
auricular vagus nerve stimulation (taVNS) was first introduced in the year
2000. The term "neuroscience" describes a range of interventional
techniques intended to control the neurological system and produce desired
results. In order to effectively stimulate the auricular vagus nerve and aid in
clinical application and healthcare, transcutaneous auricular vagus nerve
stimulators are defined as devices that are based on the corresponding
electrical output parameter with pulse width, frequency, intensity, and
attached leads and electrodes.[4]
Over
the course of more than 20 years of research and application, taVNS has been
used to treat 31 different types of diseases or disorders. These include
Parkinson’s disease, schizophrenia, post-traumatic stress disorder, epilepsy,
depression, insomnia, diabetes, impaired glucose tolerance, pain, migraine,
stroke, poststroke rehabilitation, anxiety, fear, cognitive impairment, atrial
fibrillation, myocardial infarction, heart failure, arrhythmia, tachycardia,
tinnitus, Prader-Willi Syndrome (PWS), obesity, gastrointestinal dysfunction,
postoperative intestinal obstruction, inflammatory bowel disease, colon cancer,
and dystonia [4]
There are two ways to
approach transcutaneous VNS: by stimulating the auricular branch or the
cervical bundle. Clinicians in several professions say that transcutaneous VNS
can be applied to a larger group of patients and is even comfortable for
patients with non-life-threatening diseases because there is no need for
surgical treatments. A more recent delivery method called transcutaneous
auricular vagus nerve stimulation (taVNS) makes use of an electrical
transcutaneous stimulation device. positioned at the tragus or concha of the
ear[3]
Transcutaneous auricular vagus nerve
stimulation (taVNS) is a noninvasive method of VNS via transcutaneous
stimulation of the peripheral auricular branch of the vagus nerve and regarded
as a potentially safer, better-tolerated method for sensory and motor recovery
in chronic stroke [7]
Similar to implanted
vagal nerve stimulation (iVNS), transcutaneous auricular VNS (TAVNS) stimulates
vagal projections and vagally mediated pathways in a safe, well-tolerated,
non-invasive manner. At the cymba and cavum conchae, the auricular branch of the
vagus nerve (ABVN) is the only branch of the vagus to reach the skin. [1]
In individuals who have had a persistent
stroke, TaVNS in conjunction with rehabilitation has been shown to enhance
upper limb motor dysfunction and raise UE-FM scale scores.[2]
TaVNS
has been shown to increase Growth differentiation factor 11 (GDF11) expression
in the peri-infarct cortex. GDF11 is a member of the transforming growth
factor-β (TGF-β) superfamily. GDF11 has been shown to increase markers of
neurogenesis and angiogenesis to improve neurological function after stroke.
These results suggest that TVNS can improve upper limb motor dysfunction after
stroke to some extent and may be an adjunctive intervention for recovery of
limb function after stroke. TVNS’s safety, affordability, ease of use, and
noninvasive nature make it a potential novel strategy for motor sensory
rehabilitation in chronic stroke patients.[2]
As a result of the electrode placement, local
skin irritation, headaches, and nasopharyngitis are the only moderate side
effects of transcutaneous vagus nerve stimulation, according to the author’s
conclusion [3]
NEED FOR THE STUDY:
Patients who have experienced
a stroke disrupt their motor function as well as their cognitive function.
While some studies have demonstrated the effects of transcutaneous auricular
vagus nerve stimulation in conjunction with conventional rehabilitation, very
few have examined the combined effects of these two interventions. This study
takes an innovative approach to improving both motor and cognitive function in
stroke rehabilitation
RESEARCH QUESTION
Is
there any effect of transcutaneous auricular vagus nerve stimulation on
recovery of upper limb motor and cognitive function in stroke patients?
AIM AND
OBJECTIVES:
AIM:
To find out the
effect of transcutaneous auricular vagus nerve stimulation on recovery of upper
limb motor and cognitive function in stroke patients
OBJECTIVES:
To find out the effectiveness
of transcutaneous auricular vagus nerve stimulation on motor function along
with conventional rehabilitation
To find out the effectiveness
of transcutaneous auricular vagus nerve stimulation on cognitive function along
with conventional rehabilitation
Hypotheses
Null Hypothesis (H0):
There will not be significant effect of transcutaneous
auricular vagus nerve stimulation on recovery of upper limb motor and cognitive
function in stroke patients.
Alternative Hypothesis
(H1):
There will be significant
effect of transcutaneous auricular vagus nerve stimulation on recovery of upper
limb motor and cognitive function in stroke patients.
MATERIAL AND METHODOLOGY Study setting: The study will be conducted at department of Neuroscience
Physiotherapy, Dr. A.P.J Abdul Kalam college of physiotherapy, Loni. Study Design: Randomized controlled trial Study
Duration: 2 years Sampling Method: Simple random sampling Sample size: 36
OUTCOME MEASURES
Outcome measures used
for this study will be as follows,
1.
Montreal cognitive assessment [0.92,
p<0.001]
2.
Action reach arm test for
assess upper extremity performance [0.996-0.998]
3.
Stroke impact scale [ICC=0.07
to 0.92]
SELECTION CRITERIA:
Inclusion criteria:
Ø Patient with subacute stroke
Ø Brunnstrom recovery stage 2
Ø Difficulty in upper limb movement
Ø MMSC score more than 24
Ø Ability to give informed consent
Ø Males and females
Ø Age 18 to 60 years
Exclusion criteria:
Participants excluded
will be:
Ø Participants who are not willing to participate in study
Ø Patients having addiction
Ø Currently taking medication to improve cognitive function
Ø Any metabolic disorder
Ø Other neurological or musculoskeletal problem
Ø Cochlear implant
Procedure INTERVENTION:
GROUP
A [TaVNS
+CONVENTIONAL THERPAY]
For TaVNS
Duration
4 week [20 Working day]
5
times week
Stimulation
parameter: 0.3ms square pulses at 20HZ for 30 second
For conventional
·
Motor component:
a.
Patient education
b.
Weight bearing
c.
proprioceptive neuro muscular
facilitation
Congnitive component: Task oriented exercise
GROUP B [CONVENTIONAL THERPAY]
·
Motor component:
1.
Patient education
2.
Weight bearing
3.
proprioceptive neuro muscular
facilitation
Congnitive component: Task oriented
exercise
REFERENCE 1. 1 Li
ZD, Qiu HJ, Wang XQ, Zhang CC, Zhang YJ. Protocol: Transcutaneous auricular
vagus nerve stimulation in poststroke cognitive impairment: protocol for a
randomised controlled trial. BMJ Open. 2022;12(10).
2. Yan L, Qian Y, Li H.
Transcutaneous Vagus Nerve Stimulation Combined with Rehabilitation Training in
the Intervention of Upper Limb Movement Disorders After Stroke: A Systematic
Review. Neuropsychiatric Disease and Treatment. 2022 Jan 1:2095-106.
3. Kim AY, Marduy A, de Melo PS,
Gianlorenco AC, Kim CK, Choi H, Song JJ, Fregni F. Safety of transcutaneous
auricular vagus nerve stimulation (taVNS): A systematic review and
meta-analysis. Scientific Reports. 2022 Dec 21;12(1):22055. 4. Wang L, Wang Y, Wang Y, Wang
F, Zhang J, Li S, Wu M, Li L, Rong P. Transcutaneous auricular vagus nerve
stimulators: a review of past, present, and future devices. Expert Review of
Medical Devices. 2022 Jan 2;19(1):43-61. 5. Baig SS, Kamarova M, Ali A,
Su L, Dawson J, Redgrave JN, Majid A. Transcutaneous vagus nerve stimulation
(tVNS) in stroke: the evidence, challenges and future directions. Autonomic
Neuroscience. 2022 Jan 1;237:102909. 6. Colombo M, Aggujaro S,
Lombardi N, Pedrocchi A, Molteni F, Guanziroli E. Motor and cognitive
modulation of a single session of transcutaneous auricular vagus nerve
stimulation in post stroke patients: a pilot study. IEEE Open Journal of
Engineering in Medicine and Biology. 2023 Apr 21. 7. Wu D, Ma J, Zhang L, Wang S,
Tan B, Jia G. Effect and safety of transcutaneous auricular vagus nerve
stimulation on recovery of upper limb motor function in subacute ischemic
stroke patients: a randomized pilot study. Neural Plasticity. 2020 Oct;2020 8. Li JN, Xie CC, Li CQ, Zhang
GF, Tang H, Jin CN, Ma JX, Wen L, Zhang KM, Niu LC. Efficacy and safety of
transcutaneous auricular vagus nerve stimulation combined with conventional
rehabilitation training in acute stroke patients: a randomized controlled trial
conducted for 1 year involving 60 patients. Neural regeneration research. 2022
Aug;17(8):1809. 9. Engineer ND, Kimberley TJ,
Prudente CN, Dawson J, Tarver WB, Hays SA. Targeted vagus nerve stimulation for
rehabilitation after stroke. Frontiers in neuroscience. 2019 Mar 29; 13:280. 10. Smith T, Gildeh N, Holmes C.
The Montreal Cognitive Assessment: validity and utility in a memory clinic
setting. The Canadian Journal of Psychiatry. 2007 May;52(5):329-32. 11. Duncan PW, Wallace D, Lai SM,
Johnson D, Embretson S, Laster LJ. The stroke impact scale version 2.0:
evaluation of reliability, validity, and sensitivity to change. Stroke. 1999
Oct;30(10):2131-40.
12. McDonnell M. Action research
arm test. Aust J Physiother. 2008 Jan 1;54(3):220.
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