mHealth India Postnatal Health Intervention Effectiveness

Recruiting N/A Interventional Study
Health Knowledge, Attitudes, Practice Post Partum Depression Breastfeeding Nutrition, Healthy
No Placebo Group Every participant receives an active treatment — no one gets a placebo.
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At a Glance
Age
18 – 49
Sex
Female
Study type
Interventional
Purpose
Prevention
Participants needed
2,100 (estimated)
Sponsor
University of California, San Francisco · Other
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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 estima…
Trial Locations
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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 prov…
Contacts

Alison M El Ayadi, ScD

415-476-5877

alison.elayadi@ucsf.edu

CONTACT

Nadia G Diamond-Smith, PhD

415-476-5616

nadia.diamond-smith@ucsf.edu

CONTACT