Transcutaneous Auricular Vagus Nerve Stimulation in Upper Extremity Lymphedema
Quality of Life, Lymphedema, Hand Grasp
About this trial
This is an interventional screening trial for Quality of Life focused on measuring Lymphedema, Hand Grip, Grip Strength, Quality of Life
Eligibility Criteria
Inclusion Criteria: Between the ages of 18-65 Diagnosed with secondary lymphedema disease by the physician Minimum of three months after surgery Stage 2 and 3 patients Native speaker Turkish Individuals who agreed to participate in the study Exclusion Criteria: Individuals with any neurological or orthopedic problems in the upper extremity Individuals undergoing upper extremity surgery Presence of cardiac edema Presence of arterial disease Presence of acute venous disease Those with sensory impairment Those with cardiac rhythm disorders Individuals with cooperation problems
Sites / Locations
Arms of the Study
Arm 1
Arm 2
Arm 3
Placebo Comparator
Sham Comparator
Active Comparator
Complex Decongestive Treatment
Sham transcutaneous vagus nerve stimulation
Transcutaneous vagus nerve stimulation
Complex Decongestive Treatment (manual lymph drainage, skin care, special exercises, compression) approach. It will be applied 5 days a week for 3 weeks.
In sham transcutaneous vagus nerve stimulation application, the device electrode will be placed in the superior scapha region of the outer ear, where the vagus nerve has no innervation, and no current will be given.Complex Decongestive Therapy and sham transcutaneous vagus nerve stimulation.It will be applied 5 days a week for 3 weeks.
Transcutaneous vagus nerve stimulation will be applied in addition to Complex Decongestive Therapy.It will be applied 5 days a week for 3 weeks.