The effect of foot reflexology massage on the rate of well-being and death anxiety in patient undergoing CABG
- Conditions
- Well_being and death anxiety in patient undergoing CABG.Atherosclerotic heart disease of native coronary arteryI25.1
- Registration Number
- IRCT20110906007494N32
- Lead Sponsor
- Mazandaran University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 66
Age 18 years and above
Candidates for coronary artery bypass graft surgery
Lack of pulmonary drainage and discharge more than 200 cc per hour
Their vital signs are stable (blood pressure, temperature, pulse, respiration)
No left ventricular ejection fraction less than 35%
No communication problems (hearing, vision or speech disorders)
Non-use of drugs and alcohol
Lack of treatment for mental illness
Do not take antihistamines, antidepressants or antihistamines 4 hours before the intervention
Absence of severe neuropathy in the patient
Absence of infection or sores on the soles of the feet
No limb amputation
No history of osteoarthritis or rheumatoid arthritis
No valve replacement or repair
No need for intra-aortic pump balloons and no intubation for more than 24 hours
Lack of previous experience in massage or acupuncture during the last 3 weeks
Get a score of 45 or higher from the Templer Death Anxiety Questionnaire, which indicates the presence of death anxiety
The patient's unwillingness to cooperate during the research
The critical condition of the patient and the patient's return to the operating room
The need to take antidepressants, antidepressants, and antihistamines while studying
Death of the patient
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Well_being. Timepoint: For the intervention and control group, on the day before the operation and on the fourth day after the operation. Method of measurement: Subjective Well-being.;Death anxiety. Timepoint: For the intervention and control group, on the day before the operation and on the fourth day after the operation. Method of measurement: Templer questionnaire.
- Secondary Outcome Measures
Name Time Method