Effectiveness of CBT and Attentional Bias Modification on the Anxiety of the Pregnant Wome
Not Applicable
- Conditions
- Anxiety.Anxiety disorder due to known physiological condition
- Registration Number
- IRCT20180922041082N1
- Lead Sponsor
- Kerman University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- Female
- Target Recruitment
- 75
Inclusion Criteria
age between 18-35 years
primigravid
gestational age 14-28 weeks
low-risk pregnancy
desired pregnancy
low to moderate anxiety scores
having at least a middle school education
willing to attend the educational sessions
ability of doing homework
Exclusion Criteria
pregnancy complications such as bleeding, diabetes, hypertension, preterm delivery and internal illness
use of anxiolytics and anti-depressants
having encountered with severe stress during the intervention period e.g., the death of first-degree relatives, divorce, spouse in prison.
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Anxiety levels in pregnant women. Timepoint: Measure anxiety level before intervention, immediately after intervention, one month after intervention. Method of measurement: Spielberger State-Trait Anxiety Inventory.
- Secondary Outcome Measures
Name Time Method