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Search / Trial NCT05268588

mHealth India Postnatal Health Intervention Effectiveness

Launched by UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · Feb 24, 2022

Trial Information

Current as of June 26, 2025

Recruiting

Keywords

M Health Group Care

ClinConnect Summary

This clinical trial, called the mHealth India Postnatal Health Intervention Effectiveness study, is looking to see how effective a mobile phone-based education and support program is for new mothers in India. The program aims to provide helpful information and support about health practices after giving birth, such as breastfeeding, nutrition, and managing postpartum depression. Researchers will compare the outcomes of women who receive this mobile support along with standard postpartum care to those who only receive the usual care. The study involves 2,100 women across three different states in India and will analyze how this program impacts their health knowledge, behaviors, and overall health.

To participate in this trial, women need to be between 28 and 32 weeks pregnant, speak the local language, and either have their own mobile phone or be willing to use a study phone. They must also be able to understand and agree to participate in the study. If eligible, participants can expect to receive valuable information and support through their phones, helping them improve their health and well-being after childbirth. The study is currently recruiting participants, and it aims not only to assess health outcomes but also to understand how knowledge, social support, and confidence can lead to positive changes in health behaviors.

Gender

FEMALE

Eligibility criteria

  • 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

About University Of California, San Francisco

The University of California, San Francisco (UCSF) is a leading academic institution renowned for its commitment to advancing healthcare through innovative research and clinical trials. With a focus on translating scientific discoveries into effective therapies, UCSF collaborates with a diverse array of stakeholders, including healthcare professionals, industry partners, and patient communities. The university's research programs emphasize interdisciplinary approaches and leverage cutting-edge technology to address complex medical challenges. As a sponsor of clinical trials, UCSF is dedicated to maintaining the highest standards of ethical conduct and scientific rigor, ensuring the safety and well-being of participants while contributing to the broader medical knowledge base.

Locations

New Delhi, Delhi, India

Chandigarh, Haryana, India

Bhopal, Madhya Pradesh, India

Patients applied

0 patients applied

Trial Officials

Alison M El Ayadi, ScD

Principal Investigator

University of California, San Francisco

Nadia G Diamond-Smith, PhD

Principal Investigator

University of California, San Francisco

Timeline

First submit

Trial launched

Trial updated

Estimated completion

Not reported

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