| CTRI Number |
CTRI/2024/12/078441 [Registered on: 23/12/2024] Trial Registered Prospectively |
| Last Modified On: |
20/12/2024 |
| Post Graduate Thesis |
No |
| Type of Trial |
Interventional |
|
Type of Study
|
Medical Device Physiotherapy (Not Including YOGA) |
| Study Design |
Randomized, Parallel Group, Placebo Controlled Trial |
|
Public Title of Study
|
Transcutaneous Electrical Stimulation of Vagus Nerve Among Stroke survivors |
|
Scientific Title of Study
|
Efficacy and safety of Transcutaneous Electrical Stimulation of Vagus Nerve in Upper Limb Motor Recovery Among Stroke survivors: A Randomized Controlled Trial |
| Trial Acronym |
NIL |
|
Secondary IDs if Any
|
| Secondary ID |
Identifier |
| NIL |
NIL |
|
|
Details of Principal Investigator or overall Trial Coordinator (multi-center study)
|
| Name |
Dr Sandip Dhole |
| Designation |
Associate Professor |
| Affiliation |
AIIMS, Bibinagar |
| Address |
PMR Department
AIIMS, Bibinagar
(Hyderabad Metropolitan Region)
Bibinagar, Dist.Yadadari Bhuvanagiri,
Telangana-508126 AIIMS, Bibinagar
(Hyderabad Metropolitan Region)
Bibinagar, Dist.Yadadari Bhuvanagiri,
Telangana-508126 Nalgonda TELANGANA 508126 India |
| Phone |
9867927350 |
| Fax |
|
| Email |
drsandipdhole@gmail.com |
|
Details of Contact Person Scientific Query
|
| Name |
Dr Sandip Dhole |
| Designation |
Associate Professor |
| Affiliation |
AIIMS, Bibinagar |
| Address |
PMR Department
AIIMS, Bibinagar
(Hyderabad Metropolitan Region)
Bibinagar, Dist.Yadadari Bhuvanagiri,
Telangana-508126 AIIMS, Bibinagar
(Hyderabad Metropolitan Region)
Bibinagar, Dist.Yadadari Bhuvanagiri,
Telangana-508126
TELANGANA 508126 India |
| Phone |
9867927350 |
| Fax |
|
| Email |
drsandipdhole@gmail.com |
|
Details of Contact Person Public Query
|
| Name |
Dr Sandip Dhole |
| Designation |
Associate Professor |
| Affiliation |
AIIMS, Bibinagar |
| Address |
PMR Department
AIIMS, Bibinagar
(Hyderabad Metropolitan Region)
Bibinagar, Dist.Yadadari Bhuvanagiri,
Telangana-508126 AIIMS, Bibinagar
(Hyderabad Metropolitan Region)
Bibinagar, Dist.Yadadari Bhuvanagiri,
Telangana-508126 Nalgonda TELANGANA 508126 India |
| Phone |
9867927350 |
| Fax |
|
| Email |
drsandipdhole@gmail.com |
|
|
Source of Monetary or Material Support
|
| AIIMS, Bibinagar
(Hyderabad Metropolitan Region)
Bibinagar, Dist.Yadadari Bhuvanagiri,
Telangana-508126 |
|
|
Primary Sponsor
|
| Name |
NA |
| Address |
NA |
| Type of Sponsor |
Other [NA] |
|
|
Details of Secondary Sponsor
|
| Name |
Address |
| NIL |
NIL |
| NIL |
NIL |
|
|
Countries of Recruitment
|
India |
|
Sites of Study
|
| No of Sites = 1 |
| Name of Principal
Investigator |
Name of Site |
Site Address |
Phone/Fax/Email |
| DR SANDIP DHOLE |
AIIMS, Bibinagar |
AIIMS, Bibinagar
(Hyderabad Metropolitan Region)
Bibinagar, Dist.Yadadari Bhuvanagiri,
Telangana-508126 Nalgonda TELANGANA |
09867927350
drsandipdhole@gmail.com |
|
|
Details of Ethics Committee
|
| No of Ethics Committees= 1 |
| Name of Committee |
Approval Status |
| AIIMS BBN Ethical Committee |
Approved |
|
|
Regulatory Clearance Status from DCGI
|
|
|
Health Condition / Problems Studied
|
| Health Type |
Condition |
| Patients |
(1) ICD-10 Condition: G811||Spastic hemiplegia, |
|
|
Intervention / Comparator Agent
|
| Type |
Name |
Details |
| Comparator Agent |
sham stimulation with the clip electrodes placed at Cymba conchae at the left ear for 30 minutes, once a day, six days per week for 3 weeks followed by rehabilitation therapy only 3week course of 2h therapy sessions, 3x week at least 300 to 400 movements per session.
|
Group B will get sham stimulation with the clip electrodes placed at Cymba conchae at the left ear for 30 minutes, once a day, six days per week for 3 weeks followed by rehabilitation therapy only 3week course of 2h therapy sessions, 3x week at least 300 to 400 movements per session.
|
| Intervention |
Vagus nerve stimulation using TENS |
The Group A will get Vagus nerve stimulation using TENS with the clip electrodes placed at the Cymba conchae at the left ear 0.3ms pulses, 30Hz, intensity maximum tolerable level for 30 minutes, once a day six days per week for 3 weeks with continuous monitoring of vital parameter in presence of a senior physiotherapist and emergency medical care and also underwent rehabilitation therapy only 3 week course of
h therapy sessions, 3x week, at least 300 to 400 movements per session.
|
|
|
Inclusion Criteria
|
| Age From |
18.00 Year(s) |
| Age To |
80.00 Year(s) |
| Gender |
Both |
| Details |
1.Age: 18 years and above.
2.Patients having an ischemic stroke for at least 3 months previously
3.No strict cut-offs will be required for baseline upper limb function as long as the
4.Participant could engage with the therapist and perform the limb movements.
|
|
| ExclusionCriteria |
| Details |
1.Patients having impairments of upper limb function other than those caused by stroke
2.Hemorrhagic Stroke
3.Patients having aphasia or cognitive difficulties severe enough to interfere with the informed consent process, task specific practice or communication of adverse events,
4.Pregnant or trying to get pregnant patients
5.Patients having a pacemaker or other implanted electrical device
6.Patients having severe spasticity (a Modified Ashworth Score12 ≥3).
7.Low hearth rate (<60 bpm);
8.Apraxia
9.Excessive pain in any joint of the paretic extremity
10.Advanced liver, kidney, cardiac, or pulmonary disease
11.History of significant alcohol or drug abuse
12.Depression or use of neuropsychotropic drugs such as antidepressants or benzodiazepines
|
|
|
Method of Generating Random Sequence
|
Computer generated randomization |
|
Method of Concealment
|
An Open list of random numbers |
|
Blinding/Masking
|
Outcome Assessor Blinded |
|
Primary Outcome
|
| Outcome |
TimePoints |
Demographics, time since stroke, medication and vascular risk factors will be obtained from participants. Hospital records and imaging results will be viewed to record the size, location and precise date of the stroke.
Two measures of upper limb movement and functional independence will be assessed:
1. Upper Limb Fugl-Meyer (UFM)
2. Action Recovery Arm Test (ARAT).
|
These assessments will be performed at baseline and at the end of the intervention (3
weeks). To observe long-term effects, evaluation will be done at 6 weeks and 12 weeks after
first intervention. |
|
|
Secondary Outcome
|
|
|
Target Sample Size
|
Total Sample Size="30" Sample Size from India="30"
Final Enrollment numbers achieved (Total)= "Applicable only for Completed/Terminated trials"
Final Enrollment numbers achieved (India)="Applicable only for Completed/Terminated trials" |
|
Phase of Trial
|
Phase 3 |
|
Date of First Enrollment (India)
|
01/01/2025 |
| Date of Study Completion (India) |
Applicable only for Completed/Terminated trials |
| Date of First Enrollment (Global) |
Date Missing |
| Date of Study Completion (Global) |
Applicable only for Completed/Terminated trials |
|
Estimated Duration of Trial
|
Years="1" Months="1" Days="1" |
|
Recruitment Status of Trial (Global)
|
Not Yet Recruiting |
| Recruitment Status of Trial (India) |
Not Yet Recruiting |
|
Publication Details
|
N/A |
|
Individual Participant Data (IPD) Sharing Statement
|
Will individual participant data (IPD) be shared publicly (including data dictionaries)?
Response - NO
|
|
Brief Summary
|
Stroke is a neurological condition caused by vascular
problems such as cerebral infarction and/or intra cerebral or subarachnoid
hemorrhage1. Motor impairment occurs in 85% of patients with stroke, and it is
considered one of the main problems resulting from this condition.
Efforts have been made to develop therapies that can improve
motor impairment in stroke patients 8 Among these therapies are:
constraint-induced movement 9, mirror therapy 10 and resistance training 11,
however, these interventions have a low level of adherence 12 and the evidence
supporting their effects is still weak 9-11
Recently, Vagus Nerve Stimulation (VNS) has been proposed as
an intervention that could have beneficial effects in the recovery of motor
function in these patients, since it contributes to the generation of adaptive
neuroplasticity and the activation of neuromodulators that reduce brain
inflammation 13, 14
Objective of our study to study the efficacy and safety of
Transcutaneous Electrical Stimulation of Vagus Nerve in Upper Limb Motor Recovery
among Stroke survivors.
We are going to do prospective randomized study on stroke
patients having upper limb motor impairment.
The subject will comprise of clinically diagnosed stroke
patients in OPD and IPD at AIIMS Bibinagar, Hospital, fulfilling the inclusion
criteria of the study. In this study we are going to enroll patients by
stratified randomization in two groups 30 in each group.
The Group A will get Vagus nerve stimulation using TENS with
the clip electrodes placed at the Cymba conchae at the left ear (0.3ms pulses,
30Hz, intensity = maximum tolerable level) for 30 minutes, once a day, six days
per week for 3 weeks with continuous monitoring of vital parameter in presence
of a senior physiotherapist and emergency medical care and also underwent
rehabilitation therapy only (3-week course of 2-h therapy sessions, 3x week, at
least 300 to 400 movements per session).
Group B will get sham stimulation with the clip electrodes
placed at Cymba conchae at the left ear for 30 minutes, once a day, six days
per week for 3 weeks followed by rehabilitation therapy only (3-week course of
2-h therapy sessions, 3x week, at least 300 to 400 movements per session).
Outcome will be measured after 3 weeks of treatment by Upper
Limb Fugl-Meyer (UFM) and Action Recovery Arm Test. To observe long-term
effects, evaluation will be done at 6 weeks and 12 weeks after first
intervention.
The main safety outcome measure will be the number of
serious adverse events related to the device or therapy, such as skin toxicity
(pain, skin erythema, burns, etc.), hoarseness, and dysphasia. Heart rate (HR)
and blood pressure (BP) will also observe before and after each intervention.
Outcome Assessor will be blinded to study group allocation.
We are going to compare the results of these two groups to
see efficacy and safety of vagus nerve stimulation in stroke patients of upper
limb motor recovery. |