Clinical Research Directory

Inclusion Criteria: Who volunteered to participate in the study, * those who are 18 years of age or older, * Without communication difficulties and mental disabilities related to vision, hearing and speech, * Hypertension problem has been controlled, * Blood pressure measurement does not need to be performed on an outpatient basis, * Any complications after surgery (bleeding, nausea, vomiting, etc.) that did not occur, * Application of cholecystectomy surgery, * Having a pain assessment score of 4 and above after surgical intervention, * For patients in the experimental group; infectious disease on the skin, local infection, open lesion/wound, scar tissue, edema,hematoma, thrombophlebitis, deep vein thrombosis, lymphangitis, coagulation disorder, varicose veins, osteoporosis, osteomyelitis, hepatitis, inflammatory and degenerative joint diseases, advanced neuropathy due to diabetes, on the toes deformity, November, who has not recently experienced fractures, dislocations, ruptures of muscle fibers, tendons or fascia, * Analgesic is not applied before the first attempt, which is planned to be applied after the operation, * Any medication, etc. without substance abuse, \* No chronic pain in any part of the body, * All patients who are not pregnant will be included in the sample. Exclusion Criteria: Any complications such as severe bleeding, nausea, vomiting develop after surgical intervention., * Patient-controlled analgesia (HKA) is applied for pain control after surgical intervention * Patients who have at least one drain placed at the surgical site are excluded from the sample, as this may affect the level of pain he will be released. Termination Criteria: The individual feels uncomfortable during the application or to leave the study if he wants, the work will be terminated.