Condition 1: Pre-Operative Anxiety. Condition 2: Operative Fear. Condition 3: Hemodynamic Parameters. Condition 4: Hemodynamic Parameters. Condition 5: Hemodynamic Parameters. Anxiety disorder due to known physiological condition Fear of other medical care Encounter for examination of blood pressure Tachycardia, unspecified Bradycardia, unspecified
Conditions
Interventions
Intervention 1: Intervention group 1: After obtaining informed consent from participants, data collection will be conducted using a questionnaire format. All patients in the intervention group (1), wi
Sponsors
College of Nursing, University of Baghdad
Eligibility
Sex/Gender
All
Age
18 Years to 75 Years
Inclusion criteria
Inclusion criteria: Adult patients undergoing CAPG Patient having the ability to communicate and willing to participate in the study Patient should not have significant cognitive impairment that would hinder participation in VR and Yoga therapy
Exclusion criteria
Exclusion criteria: Patient having hearing and vision impairment. Patient who takes anti-anxiety medication Patient who refuses to participate in the study Patient with significant cardiac arrhythmia. Induvial with history of substance abuse
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Pre-Operative Anxiety, Fear for Patients with Coronary Artery Bypass Graft. Timepoint: Application of each intervention of Virtual Reality and Pranayama technique that carried out before 2 days before operation. The Virtual Reality and pranayama technique groups will take 5 sessions twice daily and the final session will be immediately pre-operative at the day of operation, each session duration will be from 15-20 minutes. Method of measurement: Measurement method before intervention and after intervention (immediately before operation for patient with CBAG) by using anxiety and fear scale (The Amsterdam Preoperative Anxiety and Information Scale (APAIS)).;Pre-Operative hemodynamic parameters for patients with coronary artery bypass graft (relief or minimize and stabilize hemodynamic parameters. Timepoint: Application of each intervention of Virtual Reality and Pranayama technique that carried out before 2 days before operation. The Virtual Reality and pranayama technique groups will take 5 sessions twice daily and the final session will be immediately pre-operative at the day of operation, each session duration will be from 15-20 minutes. Method of measurement: Measurement method before intervention and after intervention (immediately before operation for patient with CBAG) by using hemodynamic parameters measurement (vital signs) (Comen device and no. serial: K9190830012 ). | — |
Secondary
| Measure | Time frame |
|---|---|
| Minimizing or relief anxiety and fear pre-CABG. Timepoint: The secondary outcome is measured immediately preoperative in operation room when patient sitting on the surgical bed. Method of measurement: By using questionnaire (Amsterdam Preoperative Anxiety and Information Scale (APAIS)).;Stabilize hemodynamic parameters pre-CABG. Timepoint: The secondary outcome is measured immediately preoperative in operation room when patient sitting on the surgical bed. Method of measurement: Hemodynamic parameters by use computer monitor ( Comen device no. serial: K9190830012 ). | — |
Countries
Iraq
Contacts
Public ContactAlaa Jawad Kadhim
University of Baghdad/college of Nursing
Outcome results
None listed