Transcutaneous Auricular Vagus Nerve Stimulation Added to Physiotherapy for Adhesive Capsulitis

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18-65
SponsorMuhsin Doran

About this trial

This randomized, sham-controlled study will evaluate whether transcutaneous auricular vagus nerve stimulation (taVNS), when added to standard physiotherapy, improves pain, shoulder function, range of motion, and quality of life in adults with adhesive capsulitis.

A total of 40 participants aged 18 to 65 years will be randomly assigned to one of two groups. Both groups will receive 15 sessions of standard physiotherapy over 3 weeks. In addition, one group will receive active taVNS for 30 minutes per day, while the other group will receive sham stimulation for the same duration and frequency. Assessments will be performed before treatment and after the 15th treatment session using pain, shoulder disability, quality-of-life, and shoulder range-of-motion measurements.

Eligibility criteria

Qualifiers

Age between 18 and 65 years.

Clinical diagnosis of adhesive capsulitis confirmed by physical examination and, when clinically indicated, imaging.

Shoulder pain and limitation of shoulder range of motion for at least 3 months.

Provision of written informed consent.

Disqualifiers

Shoulder stiffness secondary to trauma, surgery, infection, or tumor.

Rotator cuff tear, advanced glenohumeral osteoarthritis, or inflammatory rheumatic disease.

Glucocorticoid injection into the affected shoulder within the previous 3 months.

Surgical intervention involving the affected shoulder within the previous 6 months.

Trial design

Treatments tested in this trial

  • Active Transcutaneous Auricular Vagus Nerve Stimulation (taVNS)
  • Conventional Physiotherapy
  • Sham Transcutaneous Auricular Vagus Nerve Stimulation

Treatment groups

40 Participants
are divided into 2 treatment groups

Sponsors and collaborators

Muhsin Doran

Lead sponsor

Liv Hospital Vadistanbul

Sponsor institution