search
Back to results

Mobile WACh NEO: Mobile Solutions for Neonatal Health and Maternal Support

Primary Purpose

Neonatal Death, Perinatal Death, Depression

Status
Completed
Phase
Not Applicable
Locations
Kenya
Study Type
Interventional
Intervention
Interactive two-way SMS dialogue
Sponsored by
University of Washington
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Neonatal Death focused on measuring SMS, mHealth, neonate, mortality, depression, Kenya

Eligibility Criteria

14 Years - undefined (Child, Adult, Older Adult)FemaleAccepts Healthy Volunteers

Inclusion Criteria:

  • Pregnant
  • 28-36 weeks gestation
  • Daily access to a mobile phone (own or shared) on the Safaricom network
  • Willing to receive SMS
  • Able to read and respond to text messages in English, Kiswahili or Luo, or have someone in the household who can help
  • Plan to be in the area for at least five months postpartum

Exclusion Criteria:

  • Currently enrolled in another research study
  • Previous participant in the Mobile WACh NEO RCT (i.e. with a new pregnancy)

Sites / Locations

  • Ahero Sub-District Hospital
  • Bondo Sub-County Referral Hospital
  • Rachuonyo County Hospital
  • Kisumu County Hospital
  • Mathare North Health Centre
  • Riruta Health Center

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

No Intervention

Arm Label

Interactive two-way SMS dialogue

No SMS Control

Arm Description

Participants will receive automated SMS messages with prompts to reply. They will have the ability to both respond to and initiate SMS dialogue. Trained Study Nurses will monitor and respond to participant messages.

Control receiving standard of care.

Outcomes

Primary Outcome Measures

Neonatal mortality
Death during 1st 28 days of life

Secondary Outcome Measures

Early neonatal mortality
Death during 1st 7 days of life
Initiation of early breastfeeding
Number of participants initiating breastfeeding in 1st hour of life
Exclusive breastfeeding
Cessation of exclusive breastfeeding in 1st 6 weeks of life
Thermal care
Number of participants giving infant a bath in 1st 24 hours of life
Home provision of Kangaroo Mother Care
Number of participants providing any duration of skin-to-skin care on ≥10 of the first 14 days at home, among low birthweight or preterm infants
Cord care
Number of participants with no application of substances to cord
Maternal knowledge of neonatal danger signs
Number of danger signs or symptoms successfully named
Appropriate care-seeking
Proportion of illness episodes with danger signs in which the clinic was attended and/or where the infant was hospitalized irrespective of danger signs reported in 1st 18 weeks of life (study follow-up period).
Depression
Score above diagnostic threshold (>=13) for Edinburgh Postnatal Depression Scale. Possible scores are 0-30, with a higher score indicating a higher likelihood of possible depressive illness.
Social support
Score using Medical Outcomes Study (MOS) Social Support Survey. Possible scores are 0-100, with a higher score indicating higher levels of social support.
Self-efficacy
Score using the Karitane Parenting Confidence Scale. Possible scores are 0-45, with higher scores indicating higher levels of parenting confidence.

Full Information

First Posted
October 2, 2020
Last Updated
June 23, 2023
Sponsor
University of Washington
Collaborators
Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD), Kenyatta National Hospital, Women and Infants Hospital of Rhode Island
search

1. Study Identification

Unique Protocol Identification Number
NCT04598165
Brief Title
Mobile WACh NEO: Mobile Solutions for Neonatal Health and Maternal Support
Official Title
Mobile WACh NEO Randomized Clinical Trial: Mobile Phone 2-Way Short Message Service (SMS) Versus Control to Reduce Neonatal Mortality in Kenya
Study Type
Interventional

2. Study Status

Record Verification Date
June 2023
Overall Recruitment Status
Completed
Study Start Date
September 7, 2020 (Actual)
Primary Completion Date
February 20, 2023 (Actual)
Study Completion Date
February 20, 2023 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of Washington
Collaborators
Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD), Kenyatta National Hospital, Women and Infants Hospital of Rhode Island

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
To improve neonatal mortality, it is critical to engage families, especially mothers, in essential newborn care (ENC) and appropriate care-seeking for neonatal illness as well as to support maternal mental health and self-efficacy. This randomized controlled trial (RCT) aims to determine the effect and mechanisms of a two- way mobile health (mHealth) SMS intervention, Mobile WACh NEO, on neonatal mortality, essential newborn practices, care-seeking and maternal mental health at four sites in Kenya.
Detailed Description
High-impact essential newborn care practices and interventions are available to support neonatal survival, but coverage remains a challenge in sub-Saharan Africa, where neonatal mortality is unacceptably high. Many newborns continue to die at home without health care services being sought. The reasons are multifactorial, at the societal, health system, and family levels. Decisions made within the household and the family's ability to reach care play a large part in determining neonatal outcomes. It is estimated that up to 80% of neonatal and child deaths may have delays in recognition of infant illness and decision to seek care. Two-way mobile health (mHealth) communication strategies can enable mothers to remotely interact with a healthcare worker (HCW) and receive real-time education, counseling, encouragement, motivation and decisional guidance to support care-seeking decisions and ultimately neonatal health and survival. The investigators developed a unique two-way SMS platform (Mobile WACh) that combines automated SMS messaging and dialogue with a HCW. The team adapted this approach for intensive neonatal support and evaluations (Mobile WACh NEO). Mobile WACh NEO (MWN) enhances the benefits of SMS messaging by engaging mothers with SMS communication and bringing timely information and support - asking critical questions at crucial times in order to assess the needs and health of newborns and assist in care seeking decisions. This is a randomized controlled trial of the MWN intervention among 5,020 participants (2,510 MWN arm, 2,510 control arm) to determine the effect of MWN on neonatal mortality, essential newborn care, care seeking, and maternal mental health in the first 6 weeks postpartum. Aim 1: To determine the effect of Mobile WACh NEO on neonatal mortality, compared to no SMS control. Aim 2: To examine the effect of Mobile WACh NEO on maternal implementation of essential newborn care and care seeking behavior. Aim 3: To examine the effects of Mobile WACh NEO on maternal social support, self-efficacy and depression. Finally, investigators will explore the associations between maternal mental health, implementation of essential newborn care, neonatal care seeking and participant engagement by SMS.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Neonatal Death, Perinatal Death, Depression
Keywords
SMS, mHealth, neonate, mortality, depression, Kenya

7. Study Design

Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
Participants will be randomized to 1) Interactive two-way SMS dialogue or 2) Control (no SMS), using 1:1 allocation.
Masking
None (Open Label)
Allocation
Randomized
Enrollment
5020 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Interactive two-way SMS dialogue
Arm Type
Experimental
Arm Description
Participants will receive automated SMS messages with prompts to reply. They will have the ability to both respond to and initiate SMS dialogue. Trained Study Nurses will monitor and respond to participant messages.
Arm Title
No SMS Control
Arm Type
No Intervention
Arm Description
Control receiving standard of care.
Intervention Type
Behavioral
Intervention Name(s)
Interactive two-way SMS dialogue
Intervention Description
We will utilize Mobile WACh, a human-computer hybrid system that enables seamless two-way SMS communication and patient tracking, to provide consistent support to women and their infants during the peripartum period and 6 weeks into the baby's life. Women will receive automated theoretically grounded SMS messages targeting the appropriate peripartum period and will have the capability to respond and spontaneously message a nurse based at the clinic. During pregnancy, automated SMS will be delivered weekly. Two weeks prior to the participant's estimated due date (EDD), daily messaging will begin, and will continue for two weeks after delivery is ascertained. Thereafter, SMS will be delivered every other day for the remaining four weeks. Women who experience pregnancy or infant loss will be enrolled into an infant loss track where they will receive messages of support.
Primary Outcome Measure Information:
Title
Neonatal mortality
Description
Death during 1st 28 days of life
Time Frame
28 days postpartum
Secondary Outcome Measure Information:
Title
Early neonatal mortality
Description
Death during 1st 7 days of life
Time Frame
7 days postpartum
Title
Initiation of early breastfeeding
Description
Number of participants initiating breastfeeding in 1st hour of life
Time Frame
1 hour postpartum
Title
Exclusive breastfeeding
Description
Cessation of exclusive breastfeeding in 1st 6 weeks of life
Time Frame
6-weeks postpartum
Title
Thermal care
Description
Number of participants giving infant a bath in 1st 24 hours of life
Time Frame
24 hours postpartum
Title
Home provision of Kangaroo Mother Care
Description
Number of participants providing any duration of skin-to-skin care on ≥10 of the first 14 days at home, among low birthweight or preterm infants
Time Frame
14 days at home postpartum
Title
Cord care
Description
Number of participants with no application of substances to cord
Time Frame
2-weeks postpartum
Title
Maternal knowledge of neonatal danger signs
Description
Number of danger signs or symptoms successfully named
Time Frame
6-weeks postpartum
Title
Appropriate care-seeking
Description
Proportion of illness episodes with danger signs in which the clinic was attended and/or where the infant was hospitalized irrespective of danger signs reported in 1st 18 weeks of life (study follow-up period).
Time Frame
18 weeks postpartum
Title
Depression
Description
Score above diagnostic threshold (>=13) for Edinburgh Postnatal Depression Scale. Possible scores are 0-30, with a higher score indicating a higher likelihood of possible depressive illness.
Time Frame
Enrollment through 6-weeks postpartum
Title
Social support
Description
Score using Medical Outcomes Study (MOS) Social Support Survey. Possible scores are 0-100, with a higher score indicating higher levels of social support.
Time Frame
Enrollment through 6-weeks postpartum
Title
Self-efficacy
Description
Score using the Karitane Parenting Confidence Scale. Possible scores are 0-45, with higher scores indicating higher levels of parenting confidence.
Time Frame
Enrollment through 6-weeks postpartum

10. Eligibility

Sex
Female
Minimum Age & Unit of Time
14 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Pregnant 28-36 weeks gestation Daily access to a mobile phone (own or shared) on the Safaricom network Willing to receive SMS Able to read and respond to text messages in English, Kiswahili or Luo, or have someone in the household who can help Exclusion Criteria: Currently enrolled in another research study Previous participant in the Mobile WACh NEO RCT (i.e. with a new pregnancy)
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Jennifer A Unger, MD, MPH
Organizational Affiliation
Brown University
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
John Kinuthia, MBChB, MMed
Organizational Affiliation
Kenyatta National Hospital
Official's Role
Study Director
Facility Information:
Facility Name
Ahero Sub-District Hospital
City
Ahero
State/Province
Kisumu
Country
Kenya
Facility Name
Bondo Sub-County Referral Hospital
City
Bondo
Country
Kenya
Facility Name
Rachuonyo County Hospital
City
Homa Bay
Country
Kenya
Facility Name
Kisumu County Hospital
City
Kisumu
Country
Kenya
Facility Name
Mathare North Health Centre
City
Nairobi
Country
Kenya
Facility Name
Riruta Health Center
City
Nairobi
Country
Kenya

12. IPD Sharing Statement

Plan to Share IPD
Yes
IPD Sharing Plan Description
Data from Mobile WACh NEO will be available at end of the project by contacting the study team at the University of Washington (neor01@uw.edu).
IPD Sharing Time Frame
At the end of the project.
Citations:
PubMed Identifier
34949631
Citation
Ronen K, Choo EM, Wandika B, Udren JI, Osborn L, Kithao P, Hedstrom AB, Masinde M, Kumar M, Wamalwa DC, Richardson BA, Kinuthia J, Unger JA. Evaluation of a two-way SMS messaging strategy to reduce neonatal mortality: rationale, design and methods of the Mobile WACh NEO randomised controlled trial in Kenya. BMJ Open. 2021 Dec 23;11(12):e056062. doi: 10.1136/bmjopen-2021-056062.
Results Reference
background

Learn more about this trial

Mobile WACh NEO: Mobile Solutions for Neonatal Health and Maternal Support

We'll reach out to this number within 24 hrs