Mobile health platform development after child birth.
Not yet recruiting
- Conditions
- Immediate postpartum Patients Z392Encounter for routine postpartum follow-upEncounter for routine postpartum follow-up,
- Registration Number
- CTRI/2021/01/030572
- Lead Sponsor
- Dr Rashmi Bagga
- Brief Summary
In phase 2 we will evaluate the feasibility and acceptability of two intervention component using a controlled 4 arm factorial design (n=160, 40 per arms)
1. Real time mobile voice information and support group alone 2. Asynchronous/on demand text based support group only 3. Real time mobile voice information and support group plus asynchronous/ on demand text based support group. Feasibility and acceptability will be assessed by back end data, surveys, IDIs with 30 participants and moderators.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Not Yet Recruiting
- Sex
- Female
- Target Recruitment
- 160
Inclusion Criteria
- Postnatal 2.
- 18+ years old, 3.
- postpartum period up to 2 weeks.
Exclusion Criteria
- women below 18 years of age 2.
- Women with high risk pregnancies 2.
- Women who delivered preterm, suffer severe maternal complications or they or their baby are otherwise sick in the first week.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Feasibility and acceptability will be assessed via back-end After 6 months of intervention data, surveys, and IDIs with purposively selected participants and moderators. After 6 months of intervention
- Secondary Outcome Measures
Name Time Method MCH health-related knowledge, behaviors and outcomes including exclusive breastfeeding, immunization, family planning uptake, postnatal visits, mental health and empowerment. After 6 months
Trial Locations
- Locations (1)
PGIMER, Chandigarh
🇮🇳Chandigarh, CHANDIGARH, India
PGIMER, Chandigarh🇮🇳Chandigarh, CHANDIGARH, IndiaRashmi BaggaPrincipal investigator9872494602rashmibagga@gmail.com