Development and Pilot Test of a Postnatal mHealth Intervention - Phase 2

Summary

The goal of the study is to assess the feasibility and acceptability of the optimized MeSSSSage intervention which was developed and revised based on the results of our initial pilot testing. The investigators will conduct a controlled 4-arm factorial design randomized study to test the feasibility, acceptability and preliminary effectiveness of several intervention modalities over a 6-month period.

Conditions

• Health Attitude
• Knowledge, Attitudes, Practice
• Post Partum Depression
• Acceptability of Health Care

Interventions

BEHAVIORAL

MESSSSAGE - live

mHealth education and social support intervention, synchronous via call

BEHAVIORAL

MESSSSAGE - asynchronous

mHealth education and social support intervention, asynchronous via text

Sponsors & Collaborators

• University of California, Los Angeles

  collaborator OTHER

• Post Graduate Institute of Medical Education and Research, Chandigarh

  collaborator OTHER

• Indraprastha Institute of Information Technology Delhi

  collaborator OTHER

• Survival for Women and Children Foundation

  collaborator OTHER

• Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD)

  collaborator NIH

• University of California, San Francisco

  lead OTHER

Principal Investigators

• Alison M El Ayadi, ScD · University of California, San Francisco

• Nadia G Diamond-Smith, PhD · University of California, San Francisco

Study Design

Allocation

RANDOMIZED

Purpose

PREVENTION

Masking

NONE

Model

FACTORIAL

Eligibility

Min Age

18 Years

Max Age

50 Years

Sex

FEMALE

Healthy Volunteers

No

Timeline & Regulatory

Start

2021-07-30

Primary Completion

2022-11-15

Completion

2022-11-15

Countries

• India

Study Locations