Actively Recruiting
mHealth India Postnatal Health Intervention Effectiveness
Led by University of California, San Francisco · Updated on 2026-04-01
2100
Participants Needed
3
Research Sites
123 weeks
Total Duration
On this page
Sponsors
U
University of California, San Francisco
Lead Sponsor
P
Post Graduate Institute of Medical Education and Research, Chandigarh
Collaborating Sponsor
AI-Summary
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.
CONDITIONS
Official Title
mHealth India Postnatal Health Intervention Effectiveness
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Pregnant women between 28 and 32 weeks gestational age
- Speak the local language
- Have a personal mobile phone or willing to accept a study phone
- Able to provide informed consent
You will not qualify if you...
- Do not speak the local language
- Do not have a personal phone or unwilling to accept a study phone
- Unable to provide informed consent
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 3 locations
1
Post-Graduate Institute for Medical Education and Research
Chandīgarh, Haryana, India
Actively Recruiting
2
Sangath
Bhopal, Madhya Pradesh, India
Actively Recruiting
3
Indraprastha Institute for Information Technology
New Delhi, National Capital Territory of Delhi, India
Not Yet Recruiting
Research Team
A
Alison M El Ayadi, ScD
CONTACT
N
Nadia G Diamond-Smith, PhD
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
PREVENTION
Number of Arms
2
Not the Right Trial for You?
Explore thousands of other clinical trials that might be a better match.
Sign up to get personalized trial recommendations delivered to your inbox.
Already have an account? Log in here