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Official title Effect of Transcutaneous Auricular Vagus Nerve Stimulation Application on Respiratory Functions in Stroke Patients
ClinicalTrials.gov ID: NCT06793800
What this study is testing
- What it's testing
- The purpose of this study is to evaluate the effectiveness of Transcutaneous Auricular Vagus Nerve Stimulation (TAVSS) in improving respiratory muscle strength and function in chronic stroke patients. It aims to explore TAVSS as a potential complementary approach in enhancing rehabilitation outcomes for this population.
- Which group you join is decided by chance.
A plain-language read of the study's public ClinicalTrials.gov listing. The study team confirms the details.
Who can take part
Ages 40 to 80
You may be able to join if
- Being a chronic stroke patient with an ischemic or hemorrhagic stroke diagnosis made 1-3 years ago
- Having been diagnosed with stroke for the first time
- Ability to understand and follow simple verbal instructions
- Being between the ages of 40 and 80
- No conditions affecting perioral muscles, such as facial paralysis or swallowing disorders
You likely can't join if
- Presence of infection, ulcer, or scar on the auricle
- Metallic implants in the skull, hypersensitivity, injury, or inflammation inside the ear
- Chronic pulmonary and/or cardiac diseases
- Resting heart rate below 60 beats per minute
- Devices such as pacemakers or cochlear implants
- Uncontrolled hypertension
See the full eligibility criteria
- Being a chronic stroke patient with an ischemic or hemorrhagic stroke diagnosis made 1-3 years ago
- Having been diagnosed with stroke for the first time
- Ability to understand and follow simple verbal instructions
- Being between the ages of 40 and 80
- No conditions affecting perioral muscles, such as facial paralysis or swallowing disorders
- No visual, auditory, or communication problems
- No cardiopulmonary disorders
- No additional neurological, cardiovascular, orthopedic, or similar conditions causing balance problems
- Mini Mental State Examination (MMSE) score ≥24
- No surgical operations or Botox applications in the last 6 months
- Scoring 2 or below on the Modified Ashworth Scale
- Presence of infection, ulcer, or scar on the auricle
- Metallic implants in the skull, hypersensitivity, injury, or inflammation inside the ear
- Chronic pulmonary and/or cardiac diseases
- Resting heart rate below 60 beats per minute
- Devices such as pacemakers or cochlear implants
- Uncontrolled hypertension
- Chronic obstructive pulmonary disease (COPD) or asthma unrelated to stroke
- History of surgical operation or Botox application within the last 6 months
- Presence of aphasia, apraxia, or neglect syndrome
- History of 2 or more strokes (SVO)
- Comorbid conditions affecting respiratory functions (e.g., Multiple Sclerosis, Parkinson's, spinal cord injury, contractures, deformities after fractures, active upper or lower respiratory infections, etc.)
- Lack of cooperation
The study team makes the final eligibility decision.
Where it's taking place
- Istanbul, Turkey (Türkiye)
Questions & answers
Do participants get paid in this trial?
This listing doesn't specify compensation. Many trials still reimburse travel or offer a stipend, so it's worth asking the study team when you connect.
Is it free to join, and do I need insurance?
Searching and applying through BridgeMD is free. In clinical trials the study-related treatment and visits are generally provided at no cost to you. You usually don't need insurance to take part - confirm specifics with the study team.
How long does this study last?
The listing doesn't state an exact length. The study team walks you through the schedule and number of visits before you decide to enroll.
Who can join this trial?
This study is enrolling all sexes, 40 years to 80 years. The study team makes the final eligibility decision.
Where is this trial taking place?
Study sites include Istanbul, Turkey (Türkiye). Enter your location above to see the nearest site and check your eligibility.
Explore other conditions
BridgeMD is an information and trial-matching tool - not medical advice, and not the study sponsor. Details come from ClinicalTrials.gov; the study team decides eligibility.