A study on the effectiveness of the mental health mobile application for Perinatal depressio

Not Applicable

• Conditions: Pregnancy, childbirth and the puerperium

• Registration Number: KCT0008887
• Lead Sponsor: Catholic Kwandong University International St.Mary's Hospital

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 13 November 2023

Recruitment & Eligibility

• Status: ot yet recruiting
• Sex: Female
• Target Recruitment: 88

Inclusion Criteria

(1) a pregnant woman between the ages of 19 and 65
(2) having a depression score in Depression, Anxiety, Stress Scales (DASS-21) of 5 or higher, OR a score of the Edinburgh Postnatal Depression Scale (EPDS) of 9 or higher
(3) smartphone owners
(4) meet the minimum smartphone specifications

Exclusion Criteria

(1) over 32 weeks of gestation
(2) being expected to give childbirth within 4 weeks (during the intervention period)
(3) diagnosed with bipolar or psychotic major depressive disorder
(4) diagnosed with Post-Traumatic Stress Disorder (PTSD) and Obstructive Compulsive Disorder (OCD) among psychiatric comorbidities

Study & Design

• Study Type: Interventional Study
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Depression, Anxiety and Stress Scale, 21-question version (DASS-21);Edinburgh Postnatal Depression Scale (EPDS)

Secondary Outcome Measures

Name	Time	Method
Coronavirus Anxiety Scales (CAS);Cognitive and Affective Mindfulness Scale-revised (CAMS-r);Mental Health Continuum-short form (MHC-SF);Maternal-Fetal Attachment scale (MFAS);Positive Affect and Negative Affect Schedules (PANAS)