Investigating the effect of virtual reality-based game therapy on the intensity of pain and anxiety caused by amniocentesis
Not Applicable
Recruiting
- Conditions
- Women undergoing amniocentesis.
- Registration Number
- IRCT20230507058109N2
- Lead Sponsor
- Oroumia University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- Female
- Target Recruitment
- 56
Inclusion Criteria
Willingness to participate in the study
singleton pregnancy
Gestation age 15-18 weeks
Mother's age is 18 to 45 years
Have minimum literacy
No vision and hearing impairment
Not having chronic diseases before or during pregnancy
Exclusion Criteria
Participant's unwillingness to continue cooperation during each stage of the study
History of seizures and epilepsy
Dizziness and active vomiting
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Severity of pain and anxiety caused by amniocentesis. Timepoint: Measuring anxiety caused by amniocentesis before amniocentesis and measuring anxiety caused by amniocentesis and pain intensity after amniocentesis. Method of measurement: Visual pain measurement scale and anxiety questionnaire for prenatal diagnostic procedures (perinatal).
- Secondary Outcome Measures
Name Time Method