Integrated e-Screening for Postnatal Depression and Anxiety
Not Applicable
Recruiting
- Conditions
- Postnatal depressionPostnatal anxietyMental Health - DepressionReproductive Health and Childbirth - Childbirth and postnatal careMental Health - Anxiety
- Registration Number
- ACTRN12616001217493
- Lead Sponsor
- Parent-Infant Research Institute
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- Female
- Target Recruitment
- 600
Inclusion Criteria
Ability to understand spoken and written language
Baby aged 4-6 weeks
Exclusion Criteria
nil
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Depression screening acceptability measured by a questionnaire developed specifically for this study[4-week KAS visit];Uptake: Proportion of participants receiving a depression screening assessment at the 4-week KAS visit[4-week KAS visit];Depression symptoms as measured by the Depression, Anxiety and Stress Scales (DASS-21)[3-months post-birth]
- Secondary Outcome Measures
Name Time Method Depressive Disorder measured by the Structured Clinical Interview for the DSM-5[3-months post-birth];Referral rates and types of services referred to measured by a questionnaire developed for this project[4-week KAS visit];Staff time and costs (composite outcome) measured by a questionnaire developed for this project[4-week KAS visit];Ease of implementation and integration into existing clinical systems measured by a questionnaire developed for this project and thematic analysis of qualitative data from focus group transcripts[Post-recruitment];Anxiety symptoms as measured by the Depression, Anxiety and Stress Scales (DASS-21) <br>is also a primary outcome.[3-months post-birth];Stress symptoms as measured by the Depression, Anxiety and Stress Scales (DASS-21) <br>is also a primary outcome.[3-months post-birth]