Tele-counselling on perinatal mental health during pandemics

Not Applicable

• Conditions: Condition 1: anxiety. Condition 2: depression. Condition 3: health anxiety.; Other anxiety disorders; Other depressive episodes; Other somatoform disorders; F32.8; F45.8

• Registration Number: IRCT20170611034452N12
• Lead Sponsor: Kerman University of Medical Sciences

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 5 January 2021

Recruitment & Eligibility

• Status: Complete
• Sex: Female
• Target Recruitment: 60

Inclusion Criteria

satisfaction to participate in the study
being in a time period of 28 weeks of pregnancy to 28th postpartum day for women referring for perinatal services
Not consuming psychiatric medication

Exclusion Criteria

loss of pregnancy (fetal death)

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Anxiety. Timepoint: Before and 3 weeks after intervention. Method of measurement: Modified to COVID-19 Hospital Depression and Anxiety Scale.;Depression. Timepoint: Before and 3 weeks after intervention. Method of measurement: Modified to COVID-19-Hospital Depression and Anxiety Scale.;Health anxiety. Timepoint: Before and 3 weeks after intervention. Method of measurement: Health anxiety questionnnaire.