Comparing the effectiveness of online Balint group and SSRIs in Coronavirus anxiety
Not Applicable
Completed
- Conditions
- Illness anxiety disorder.Other anxiety disorders
- Registration Number
- IRCT20200411047023N1
- Lead Sponsor
- Golestan University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- All
- Target Recruitment
- 40
Inclusion Criteria
Hospital Healthcare workers who have been in contact with COVID-19 patients
No history of previous psychiatric illness
Ability to use Skype application and participate in online sessions
Written consent for participating in the study
Diagnosis of illness anxiety after being evaluated by two psychiatrists
Exclusion Criteria
No further interest in continuing the study
More than 3 absent Balint sessions
No medication compliance
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Score in Corona Disease Anxiety Scale (CDAS). Timepoint: At the beginning of study (before intervention) and after 4 weeks. Method of measurement: Corona Disease Anxiety Scale (CDAS).
- Secondary Outcome Measures
Name Time Method Score in Connor-Davidson resilience scale. Timepoint: At the beginning of study (before intervention) and after 4 weeks. Method of measurement: Connor-Davidson resilience scale.