Condition 1: Investigating the effect of ear acupressure training on anxiety of patients after coronary artery bypass surgery. Condition 2: Investigating the effect of ear acupressure training on sleep quality of patients after coronary artery bypass surgery. Anxiety disorder, unspecified Insomnia due to medical condition
Conditions
Interventions
Intervention 1: Intervention group: Auricular acupressure intervention using special adhesives containing vaccaria seeds on points of the ear (Shen Men, zero point, pelvis, abdomen, endocrine, uterus)
Sponsors
Mazandaran University of Medical Sciences
Eligibility
Sex/Gender
All
Age
18 Years to No maximum
Inclusion criteria
Inclusion criteria: Age 18 years and above Not having any history of taking psychiatric drugs (delirium, insomnia, etc.), based on the medical history and by reviewing the patient's hospitalization file and looking at the patient's medications Patients under general anesthesia (by reading the patient procedure description sheet, after surgery, which is available in the patient file) Using only ibuprofen pain reliever based on the department's routine in the form of 400 mg every 8 hours (they should not use Gellophane 4 hours before the intervention) Creatinine in the range of 1.2 - 0.7 mg/DL
Exclusion criteria
Exclusion criteria: Patients with any history of eczema, dermatitis, etc. Complications of surgery include bleeding
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Assessment of patients' anxiety after coronary artery bypass surgery. Timepoint: Evaluation of patients' anxiety in two intervention and control groups immediately after the intervention and four days after the intervention. Method of measurement: The use of Spiel Berger questionnaire.;Evaluation of sleep quality of patients after coronary artery bypass surgery. Timepoint: Evaluation of sleep quality of patients in two intervention and control groups immediately after the intervention and four days after the intervention. Method of measurement: The use of Saint Mary's questionnaire. | — |
Secondary
| Measure | Time frame |
|---|---|
| Assessment of pain intensity in patients after coronary artery bypass surgery. Timepoint: Evaluation of pain intensity of patients in two intervention and control groups immediately after the intervention and four days after the intervention. Method of measurement: The use of Visual Analogue pain Scale.;Evaluation of hemodynamic indicators of patients after coronary artery bypass surgery. Timepoint: Evaluation of hemodynamic indicators of patients in two intervention and control groups immediately after the intervention and four days after the intervention. Method of measurement: Use of monitoring device. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactMohammad Hosseini Nejad
Mazandaran University of Medical Sciences
Outcome results
None listed