Virtual reality-based play therapy on pain and anxiety in patients with open heart surgery
Not Applicable
Recruiting
- Conditions
- Coronary Artery Disease.Atherosclerotic heart disease of native coronary arteryI25.1
- Registration Number
- IRCT20111203008286N11
- Lead Sponsor
- Tehran University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 90
Inclusion Criteria
Willingness to participate in the study
Full awareness (relative to place, time and person)
RASS +1 to -1
Having sinus rhythm during intervention
Exclusion Criteria
Occurrence of anxiety symptoms such as fear of closed spaces
History of neurological disorders (such as movement, vision and hearing disabilities)
Use of respiratory equipment such as artificial respiration
Receiving anti-anxiety or sedative drugs 24 hours before and after the intervention
Severe dysfunction of non-cardiovascular systems (for example, chronic renal failure)
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Pain. Timepoint: Before, one month after. Method of measurement: Visual Analog Scale.
- Secondary Outcome Measures
Name Time Method Anxiety. Timepoint: Before, one month after. Method of measurement: Spielberger questionnaire.