Actively Recruiting

Phase Not Applicable
Age: 18Years - 49Years
FEMALE
ID05268588

Effectiveness of an mHealth Interactive Education and Social Support Intervention for Improving Postnatal Health

Led by University of California, San Francisco · Updated on 2026-04-01

2100

Participants Needed

3

Research Sites

N/A

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

This research aims to evaluate a culturally tailored mobile interactive education and support group intervention called MeSSSSage among postpartum Indian women. The study focuses on improving health-related knowledge, behaviors, and outcomes for mothers and newborns, addressing challenges like limited postpartum care access and social isolation. It is a randomized controlled trial involving 2100 women from three diverse Indian states, intending to assess the intervention's impact, mechanisms, and cost-effectiveness. Participants in the intervention group receive 26 education and support sessions over eight months, including two prenatal and weekly postpartum sessions up to six months after birth. The sessions are delivered via audioconference and moderated by community health workers, with additional engagement through a provider-moderated group text chat. The control group receives standard postnatal care. The intervention is designed to supplement usual care and overcome barriers through mobile technology and social support. During the study, participants will be assessed on exclusive breastfeeding, postpartum depression, and family planning adoption at six months. Other outcomes include knowledge of maternal and neonatal danger signs, healthcare use, and infant vaccination. Researchers will monitor participant engagement and analyze how the intervention influences knowledge, social support, self-efficacy, and behaviors. The study also includes cost-effectiveness analyses and will follow participants for eight months to gather comprehensive data on postpartum health and well-being.

CONDITIONS

Brief Title

mHealth India Postnatal Health Intervention Effectiveness

Who Can Participate

Age: 18Years - 49Years
FEMALE

Eligibility Criteria

Eligible

You may qualify if you...

  • Pregnant women between 28 and 32 weeks gestation
  • Speak the local language
  • Have a personal mobile phone or willing to accept a study phone
  • Able to provide informed consent
Not Eligible

You will not qualify if you...

  • Do not speak the local language
  • No personal phone and unwilling to accept a study phone
  • Unable to provide informed consent

AI-Screening

AI-Powered Screening

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Run-in Period

Duration - From enrollment until birth (approximately 4 to 12 weeks depending on gestational age at enrollment)

Participants join groups of about 20 women and attend two prenatal intervention sessions to prepare for postpartum support.

2 prenatal intervention sessions (phone-based)

Outpatient Treatment

Duration - 6 months postpartum

Participants receive weekly group mHealth education and social support sessions via phone for six months postpartum, including interactive voice content, moderated group discussions, and text chats to improve maternal and neonatal health behaviors.

Weekly phone-based group sessions for up to 26 sessions

Follow-up

Duration - Up to 6 months postpartum

Participants are monitored for health-related behaviors and outcomes up to 6 months postpartum to assess intervention effectiveness.

Assessments at 6 months postpartum

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

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Research Team

A

Alison M El Ayadi, ScD

N

Nadia G Diamond-Smith, PhD

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

PREVENTION

Number of Arms

2

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Published Research Related To This Trial

Effectiveness of Kushal Maa, a group-based mhealth interactive education and social support intervention for maternal and neonatal health outcomes: study protocol for a multisite randomised controlled trial in India.

Alison M El Ayadi, Mona Duggal, Lakshmi Gopalakrishnan...

https://pubmed.ncbi.nlm.nih.gov/40578858