computerized patient decision aid system
Phase 3
- Conditions
- Delivery.Single spontaneous delivery, unspecified
- Registration Number
- IRCT2015093010777N4
- Lead Sponsor
- Mashhad University of Medical Sciences, Vice chancellor for research
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- Female
- Target Recruitment
- 400
Inclusion Criteria
Pregnant women 16 years and older; gestational age 28 week or more; singleton pregnancy.
Exclusion criteria: Women do not provide a written informed consent; unable to read and write; unable to work with a computer; women whose method of delivery is predetermined by the physician, based on their clinical condition
Exclusion Criteria
Not provided
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Decisional Conflict. Timepoint: Before the intervention and 4 till 10 weeks after of the intervention. Method of measurement: O’Connor's decisional conflict scale - University of Ottawa.;Knowledge. Timepoint: Before the intervention and 4 till 10 weeks after of the intervention. Method of measurement: true/false questions.
- Secondary Outcome Measures
Name Time Method Decisional Conflict subscales. Timepoint: Before and after of the intervention. Method of measurement: O’Connor's decisional conflict scale - University of Ottawa.