taVNS Combined With TENS on Motor Function in Stroke
Effect of Combining Transcutaneous Vagus Nerve Stimulation With Peripheral Nerve Stimulation on Upper Limb Motor Function in People With Stroke: A Single- Blinded Randomised Controlled Trial
The Hong Kong Polytechnic University
120 participants
Jan 1, 2025
INTERVENTIONAL
Conditions
Summary
the current study is a Blinded Randomised Controlled Trial investing the effectiveness of Combining Transcutaneous Vagus Nerve Stimulation with Peripheral Nerve Stimulation on Upper Limb Motor Function in People with Stroke
Eligibility
Inclusion Criteria5
- aged 55 - 75 years old;
- diagnosed with stroke confirmed by magnetic resonance imaging or computed tomography for more than 6 months;
- had volitional control of the non-paretic arm and at least minimal antigravity movement in the paretic shoulder;
- had at least 5 degrees of wrist extension in the antigravity position;
- be able to communicate
Exclusion Criteria3
- had neurological disease other than stroke, e.g., Parkinson's disease or dementia;
- ongoing healthy condition, e.g., angina pectoris, pain, or arthritis;
- had any contraindications of taVNS (metal implants in the brain, history of seizure)
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Interventions
The left cymba conchae was selected as taVNS stimulation side. The taVNS was delivered by earphone-shaped stimulators for 30 minutes with the stimulation parameters as follows: 0.3-ms square pulses at 20 Hz for 30 seconds with a duty cycle of 1:1; and the intensity of the stimulation was individually adjusted according to the tolerance of participants
The sham stimulation will be delivered with a shame model of the same device that used in the taVNS intervention. The interference of the device will display that the device is working normally while no electrical current output.
TENS will be delivered with commercial TENS machine. The stimulation parameters were as follows: continuous 0.2-ms square pulses at 100 Hz with the intensity adjusted according to the tolerance of each patient. Disposable surface electrodes of 5X5 cm2 were applied to stimulate the median nerve and the superficial radial nerve of both the affected and non-affected upper limbs. The placebo stimulation was delivered with a device that looked identical but had its internal electrical circuit disconnected.
The sham stimulation will be administered using a device that looks identical to the TENS device used in the TENS intervention. However, the internal electrical circuit of this device will be disconnected.
A physiotherapist supervised the intervention and monitored individual progress. The task-oriented training aims to improve the motor recovery of the upper limbs through the systematic and repetitive movement of shoulder, elbow, forearm, wrist and fingers. The task-oriented training will be conducted in seating position with a table in front. Each training task will be repeated for 10 repetitions per set with 1 minute of rest between sets.The progressions are repositioning from gravity eliminate to against position, improve movement quality, increasing number of sets and shortening rest period.
Locations(1)
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NCT07425756