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mHealth India Postnatal Health Intervention Effectiveness (MESSSSAGE)

Primary Purpose

Health Knowledge, Attitudes, Practice, Post Partum Depression, Breastfeeding

Status
Not yet recruiting
Phase
Not Applicable
Locations
India
Study Type
Interventional
Intervention
MESSSSAGE intervention
Sponsored by
University of California, San Francisco
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Health Knowledge, Attitudes, Practice focused on measuring mHealth, group care

Eligibility Criteria

18 Years - 49 Years (Adult)FemaleDoes not accept healthy volunteers

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

Sites / Locations

  • Indraprastha Institute for Information Technology
  • Post-Graduate Institute for Medical Education and Research
  • Sangath

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

No Intervention

Arm Label

Intervention Arm

Control Arm

Arm Description

The mHealth education and social support intervention includes tailored weekly educational content via interactive voice recognition and an android application, a phone-based provider-moderated group discussion, a provider-moderated group text chat, and referral to care as needed. Individuals are enrolled into groups of 20, have two intervention sessions prenatally and then have weekly meetings through six months postpartum for a total of 26 sessions.

Standard postnatal care.

Outcomes

Primary Outcome Measures

Exclusive breastfeeding
Proportion of participants reporting exclusive breastfeeding at 3 and 6 months
Postpartum depression
Proportion of participants reporting postpartum depression symptoms at 3 and 6 months
Postpartum family planning adoption
Proportion of participants not wanting to become pregnant immediately having started a modern contraceptive method within 6 months postpartum

Secondary Outcome Measures

Maternal and neonatal danger sign knowledge
Proportion of participants correctly identifying all maternal and neonatal danger signs by 6 months
Maternal and neonatal health care use
Proportion of participants seeking healthcare for maternal and neonatal concerns within 6 months
Neonatal preventive health care use
Proportion of participants having achieved target neonatal preventive care visits within 6 months
Infant vaccination
Proportion of participants having achieved recommended childhood vaccination schedule by 6 months

Full Information

First Posted
February 24, 2022
Last Updated
April 4, 2023
Sponsor
University of California, San Francisco
Collaborators
Post Graduate Institute of Medical Education & Research, Chandigarh, Indraprastha Institute of Information Technology, Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD), Sangath
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1. Study Identification

Unique Protocol Identification Number
NCT05268588
Brief Title
mHealth India Postnatal Health Intervention Effectiveness
Acronym
MESSSSAGE
Official Title
Effectiveness of an mHealth Interactive Education and Social Support Intervention for Improving Postnatal Health
Study Type
Interventional

2. Study Status

Record Verification Date
April 2023
Overall Recruitment Status
Not yet recruiting
Study Start Date
January 2024 (Anticipated)
Primary Completion Date
June 2026 (Anticipated)
Study Completion Date
June 2026 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University of California, San Francisco
Collaborators
Post Graduate Institute of Medical Education & Research, Chandigarh, Indraprastha Institute of Information Technology, Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD), Sangath

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
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.
Detailed Description
Maternal and infant mortality remain high in Northern India, at 167 per 100,000 live births and 49 per 1,000 live births, respectively. Access to perinatal care is increasing, yet gaps in care access and quality persist, particularly in peri-urban and rural areas. Steep drops in the perinatal continuum of care occur postpartum, with only 64% of mothers and 24% of infants receiving postpartum care, despite continuing maternal and infant risk. Ensuring continuity of high quality perinatal care into the postpartum period is key for maternal and infant health outcomes. Postpartum care and support have received less focus than other perinatal continuum of care indicators yet are important for optimizing maternal and neonatal health and wellbeing. Significant logistical, sociodemographic and sociocultural barriers impede postpartum care access in India including postpartum seclusion, women's limited mobility, and geography. To overcome these barriers and reduce women's postpartum isolation through social support, an international team of maternal and infant health researchers and clinicians developed and pilot-tested a culturally-tailored mobile interactive education and support group intervention to supplement standard postpartum care activities: Maa Shishu Swasthya Sahayak Samooh (maternal and child health support group: MeSSSSage). MeSSSSage uses a provider-moderated group approach to increase women's communication with providers, to refer them to in-person care, and to connect them with a virtual social support group. Participants are recruited in late pregnancy and have 26 education and support sessions via audioconference facilitated by community health workers (two prenatal and weekly postpartum sessions through six months), plus engage in a text chat group. Group-based mHealth models are low cost and likely to be cost-effective. The participants overcome logistical and sociocultural barriers to postnatal care, and the participants have high acceptability and efficiency when used for other health issues. The pilot study results indicated high acceptability and feasibility and suggest preliminary effectiveness on maternal knowledge of best practices for facilitating postpartum health. Understanding intervention effectiveness on maternal health behaviors, key intervention pathways, and cost-effectiveness will inform the scalability of this intervention, with the potential to inform other similar ones. The goal of this study is to assess the effectiveness of the 8-month MeSSSSage intervention in comparison to standard care alone on health-related behaviors and health outcomes in a fully powered randomized study, to test the conceptual model through analyzing the intervention's mechanisms of impact, and to determine cost-effectiveness. The investigators propose a randomized controlled trial (RCT) among 2100 postpartum Indian women living in 3 geographically diverse Indian states to estimate the impact of MeSSSSage on maternal and neonatal health-related knowledge, health-related behaviors, and health outcomes. The specific aims are to: Aim 1: Estimate the effectiveness of a mobile interactive education and support group intervention (MeSSSSage) on postpartum behaviors for optimizing maternal and neonatal health in India. Within the 8-month RCT, the investigators will test the impact of the MeSSSSage intervention compared to standard care within 2100 Indian women. The primary effectiveness outcomes are exclusive breastfeeding, met need for postpartum contraceptives, and postpartum mental health. Secondary outcomes will incorporate additional maternal health behaviors and maternal and neonatal outcomes (e.g., appropriate care-seeking for illness, etc. see Table 2). Aim 2: Characterize the mechanisms of impact of a mobile interactive education and support group intervention (MeSSSSage) on maternal and neonatal health in India. Within this RCT, the investigators will delineate the specific pathways through which the MeSSSSage intervention operates, including knowledge, social support, self-efficacy, and behavior change. The investigators will conduct mediation analyses using modern structural equation modeling and causal inference methods to identify the main drivers of the intervention impact to inform scalability. Aim 3: Determine the cost-effectiveness of a mobile interactive education and support group intervention (MeSSSSage) in improving postpartum maternal and neonatal health as compared to the standard of care. The investigators will conduct cost analyses to determine intervention and standard of care costs, paying special attention to the value of social network belonging, and calculating opportunity cost. The investigators will conduct cost-effectiveness analysis (CEA) overall and stratified by social connectedness level to estimate the incremental cost-effectiveness ratio (ICER) of MeSSSSage in increasing exclusive breastfeeding, met need for postpartum contraception, and reducing postpartum depression, as compared to standard of care. Perinatal educational and social support interventions are important for both physical and emotional well-being. The investigators anticipate that supplementing women's perinatal care within the postnatal period through an intervention approach that overcomes prevalent logistical and sociocultural challenges to care access through mHealth will have tangible impacts on the health and well-being of new mothers and infants. Estimating the impact of a mobile group intervention on maternal and infant health will inform scale-up of this accessible, acceptable, and feasible intervention among perinatal South Asian women, and can broadly inform the optimization of perinatal group care models for ensuring continuity across the full continuum of care.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Health Knowledge, Attitudes, Practice, Post Partum Depression, Breastfeeding, Nutrition, Healthy
Keywords
mHealth, group care

7. Study Design

Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
The mHealth education and social support intervention includes tailored weekly educational content via interactive voice recognition and an android application, a phone-based provider-moderated group discussion, a provider-moderated group text chat, and referral to care as needed. Individuals are enrolled into groups of 20, have two intervention sessions prenatally and then have weekly meetings through six months postpartum for a total of 26 sessions. This model will be tested against the standard of care (3 postnatal visits in the first 7 days postpartum).
Masking
None (Open Label)
Allocation
Randomized
Enrollment
2100 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Intervention Arm
Arm Type
Experimental
Arm Description
The mHealth education and social support intervention includes tailored weekly educational content via interactive voice recognition and an android application, a phone-based provider-moderated group discussion, a provider-moderated group text chat, and referral to care as needed. Individuals are enrolled into groups of 20, have two intervention sessions prenatally and then have weekly meetings through six months postpartum for a total of 26 sessions.
Arm Title
Control Arm
Arm Type
No Intervention
Arm Description
Standard postnatal care.
Intervention Type
Behavioral
Intervention Name(s)
MESSSSAGE intervention
Intervention Description
group mHealth education and social support intervention
Primary Outcome Measure Information:
Title
Exclusive breastfeeding
Description
Proportion of participants reporting exclusive breastfeeding at 3 and 6 months
Time Frame
6 months
Title
Postpartum depression
Description
Proportion of participants reporting postpartum depression symptoms at 3 and 6 months
Time Frame
6 months
Title
Postpartum family planning adoption
Description
Proportion of participants not wanting to become pregnant immediately having started a modern contraceptive method within 6 months postpartum
Time Frame
6 months
Secondary Outcome Measure Information:
Title
Maternal and neonatal danger sign knowledge
Description
Proportion of participants correctly identifying all maternal and neonatal danger signs by 6 months
Time Frame
6 months
Title
Maternal and neonatal health care use
Description
Proportion of participants seeking healthcare for maternal and neonatal concerns within 6 months
Time Frame
6 months
Title
Neonatal preventive health care use
Description
Proportion of participants having achieved target neonatal preventive care visits within 6 months
Time Frame
6 months
Title
Infant vaccination
Description
Proportion of participants having achieved recommended childhood vaccination schedule by 6 months
Time Frame
6 months

10. Eligibility

Sex
Female
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
49 Years
Accepts Healthy Volunteers
No
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
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Alison M El Ayadi, ScD
Phone
415-476-5877
Email
alison.elayadi@ucsf.edu
First Name & Middle Initial & Last Name or Official Title & Degree
Nadia G Diamond-Smith, PhD
Phone
415-476-5616
Email
nadia.diamond-smith@ucsf.edu
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Alison M El Ayadi, ScD
Organizational Affiliation
University of California, San Francisco
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Nadia G Diamond-Smith, PhD
Organizational Affiliation
University of California, San Francisco
Official's Role
Principal Investigator
Facility Information:
Facility Name
Indraprastha Institute for Information Technology
City
New Delhi
State/Province
Delhi
Country
India
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Pushpendra Singh, PhD
Email
psingh@iiitd.ac.in
Facility Name
Post-Graduate Institute for Medical Education and Research
City
Chandigarh
State/Province
Haryana
Country
India
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Mona Duggal, MD
Email
mona.duggal2@gmail.com
Facility Name
Sangath
City
Bhopal
State/Province
Madhya Pradesh
Country
India

12. IPD Sharing Statement

Plan to Share IPD
Yes
IPD Sharing Plan Description
After study completion, de-identified data will be made available to other researchers upon reasonable request and completion of a data sharing agreement.
IPD Sharing Time Frame
On study completion
IPD Sharing Access Criteria
Request of study team.

Learn more about this trial

mHealth India Postnatal Health Intervention Effectiveness

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