About this trial

The goal of this study is to assess the effectiveness of a culturally-tailored mobile interactive education and support group intervention to supplement standard postpartum care activities in comparison to standard care alone on health-related behaviors and health outcomes in a randomized controlled trial among 2100 postpartum Indian women living in 3 geographically diverse Indian states to estimate the impact on maternal and neonatal health-related knowledge, health-related behaviors, and health outcomes. The investigators also seek to characterize mechanisms of impact including knowledge, social support, self-efficacy, and behavior change, and determine the cost-effectiveness.

Eligibility criteria

Qualifiers

Pregnant (28-32 weeks gestational age)

Speak local language

Personal mobile phone or willing to accept study phone

Able to provide informed consent

Disqualifiers

Do not speak local language

No personal phone or unwilling to accept study phone

Unable to provide informed consent

Trial design

Treatments tested in this trial

  • MESSSSAGE intervention

Treatment groups

2,100 Participants
are divided into 2 treatment groups

Locations

3
Post-Graduate Institute for Medical Education and Research ChandīgarhHaryana, India
Sangath BhopalMadhya Pradesh, India
Indraprastha Institute for Information Technology New DelhiNational Capital Territory of Delhi, India

Sponsors and collaborators

University of California, San Francisco

Lead sponsor

Post Graduate Institute of Medical Education and Research, Chandigarh

Collaborator

Indraprastha Institute of Information Technology Delhi

Collaborator

Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD)

Collaborator

Sangath

Collaborator