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NCT06793800Recruiting

Effect of Transcutaneous Auricular Vagus Nerve Stimulation Application on Respiratory Functions in Stroke Patients

Effect of TAVNS Application on Respiratory Functions in Stroke Patients

Source: ClinicalTrials.gov · Last updated 1 Apr 2026

Brief summary (registry, in English)

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.

Status (registry)
Recruiting
Study type
Interventional
Enrollment
50 (estimated)
First submitted
21 Jan 2025
Start date
5 Aug 2025
Primary completion date
26 Aug 2025
Lead sponsor
Fenerbahce University
Diseases
Stroke
NCT number
NCT06793800

What you commit to

  • Study type: Interventional
  • Planned participants: 50
  • From 5 Aug 2025 to the primary completion date, 26 Aug 2025
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Devices such as pacemakers or cochlear implants

Other illness

  • 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
  • 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.)

Other

  • Lack of cooperation

Who the study is looking for

  • 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

Age in the registry: 40 years to 80 years · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Save your city in your profile to sort them by distance.

SiteCityCountrySite status
Mediworld Medical Center Physical Therapy and Rehabilitation Department
Coordinator of this site? Confirm its status
IstanbulTurkey (Türkiye)Recruiting

This page is information, not medical advice. Discuss any trial with your doctor.