Health Condition 1: O269- Pregnancy related conditions, unspecified
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Women who recently given birth (within last 6 months) Age range (18-45years) Ownership of a smartphone with Internet access Ability to understand and communicate in the language used in the study material (eg English)
Exclusion criteria
Exclusion criteria: Women with a history of severe mental illness (e.g., psychosis). Women with substance abuse disorders. Women with cognitive impairments that would hinder their ability to participate in the study. Women who are currently receiving treatment for postpartum depression or any other mental health condition. Women with high-risk pregnancies or medical complications requiring intensive medical care.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| To determine whether the use of the mobile application reduces the severity of postpartum depression symptoms compared to standard care or a control groupTimepoint: 6 months | — |
Secondary
| Measure | Time frame |
|---|---|
| To assess the feasibility and acceptability of the mobile application among postnatal mothers, healthcare providers, and guardians. To determine the impact of the mobile application on the early detection of postpartum depressive symptoms by comparing the rates of timely identification of symptoms between intervention and control groupsTimepoint: Baseline [1-2wks] immediate postpartum screening enrollment app on boarding early intervention [tracking ) moods and symptoms trackers , thereafter every 2wks- questionnaire scores ,outcomes reassesed,intervention tracked. At 8wks,12wks postpartum intervention efficacy,app engagement,psychological well being and outcomes assessment | — |
Countries
India
Contacts
Saveetha medical college and hospital