mHealth India Postnatal Health Intervention Effectiveness
Recruiting · NCT05268588 · Interventional (participants receive a specific treatment) · Lead sponsor: University of California, San Francisco
View the official record on ClinicalTrials.gov →Interventions studied
What this trial is about
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.
Who can take part
Inclusion criteria
- Pregnant (28-32 weeks gestational age)
- Speak local language
- Personal mobile phone or willing to accept study phone
- Able to provide informed consent
Exclusion criteria
- Do not speak local language
- No personal phone or unwilling to accept study phone
- Unable to provide informed consent
Where it is running
3 locations listed.
- Post-Graduate Institute for Medical Education and Research - Chandīgarh, Haryana, India
- Sangath - Bhopal, Madhya Pradesh, India
- Indraprastha Institute for Information Technology - New Delhi, National Capital Territory of Delhi, India