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Leading Advancements in the Uptake of Newborn Community Health (LAUNCH)

Primary Purpose

Breastfeeding, Exclusive, Immunization; Infection, Growth; Stunting, Nutritional

Status
Active
Phase
Not Applicable
Locations
Ethiopia
Study Type
Interventional
Intervention
Newborn Health Education
Sponsored by
University of Washington
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Breastfeeding, Exclusive focused on measuring Community health worker

Eligibility Criteria

14 Years - 49 Years (Child, Adult)FemaleDoes not accept healthy volunteers

Inclusion Criteria:

Newborn-mother pairs visited by the study staff (Enrolled women and newborns)

The following inclusion criteria will be used during recruitment:

  • Newborns should be those delivered at least one month after the start of the intervention period
  • Newborn-mother pairs will include only biological mothers
  • Newborn-mother pairs should be EOC parishioners
  • Newborn's family should have a soul father (a spiritual advisor assigned to the family in the Ethiopian Orthodox tradition)
  • Mother must have lived in the study area for at least 6 months
  • Mothers must give verbal written informed consent for themselves and their newborn

Formative focus group discussion and key informant interview participants (FGD and KII participants)

The following inclusion criteria will be used during recruitment:

  • Mothers of newborns <6 months old
  • Fathers of newborn children <6 months
  • Ethiopian Orthodox priests from the North Gondar region
  • Healthcare workers from government Health Centers (unit of primary care)
  • All participants must have established residency in the region for >6 months
  • All participant must give verbal informed consent

Exclusion Criteria:

Newborn-mother pairs visited by the study staff (Enrolled women and newborns)

The following exclusion criteria will be used during recruitment:

  • Newborns with gross developmental abnormalities that would make anthropometric measurements and interpretations difficult
  • Newborn whose mother is not a member of an EOC parish
  • Newborns whose mothers have died by the time of recruitment
  • Newborn whose family plans to re-locate away from the study site in less than 6 months

Formative focus group discussion and key informant interview participants (FGD and KII participants)

The following exclusion criteria will be used during recruitment:

- Newly established residence in the Woreda (<6 months)

Sites / Locations

  • University of Gondar

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

No Intervention

Arm Label

Intervention

Control

Arm Description

Outcomes

Primary Outcome Measures

Mid-upper arm circumference
Anthropometric Measurement using MUAC tapes
Proportion of mothers exclusive breastfeeding
Self-reported breastfeeding behavior

Secondary Outcome Measures

Immunization status
Collected from vaccination cards
Frequency of acute illness
Self reported
Frequency of hospitalization status
Self reported

Full Information

First Posted
July 26, 2021
Last Updated
September 15, 2023
Sponsor
University of Washington
Collaborators
Frankel Family Foundation, Stewardship Foundation
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1. Study Identification

Unique Protocol Identification Number
NCT05111899
Brief Title
Leading Advancements in the Uptake of Newborn Community Health
Acronym
LAUNCH
Official Title
Leading Advancements in the Uptake of Newborn Community Health (LAUNCH)
Study Type
Interventional

2. Study Status

Record Verification Date
September 2023
Overall Recruitment Status
Active, not recruiting
Study Start Date
July 11, 2022 (Actual)
Primary Completion Date
August 22, 2023 (Actual)
Study Completion Date
December 1, 2023 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of Washington
Collaborators
Frankel Family Foundation, Stewardship Foundation

4. Oversight

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

5. Study Description

Brief Summary
The primary objective of the study is to determine the impact of a behavior change intervention that partners Orthodox priests with members of the Health Development Army (HDA) and train them to conduct newborn health outreach to increase rates of early initiation of and exclusive breastfeeding through 6 months and vaccination coverage at six months. Secondary objectives include: Determine the impact of the intervention on infant growth at six months, observed and self-reported changes in nutrition and feeding practices of mother and infants, and early identification of newborn illness. Design a culturally relevant, scalable intervention for community-based newborn and infant health in Gondar in partnership with local partners, the Federal Ministry of Health, and the Gondar Regional Health Bureau.
Detailed Description
The study will test a model the leverages existing community networks to improve the health of newborns in Gondar, Ethiopia. The intervention will be implemented at the community level by pairs of trained Ethiopian Orthodox priests and members of the Heath Development Army (HDA). A list of priests serving at the EOC churches in the intervention arm will be obtained through the woreda diocese and their respective churches. All the priests will be contacted through the church leadership and asked to participate in the study intervention. The intervention will be implemented in collaboration with HDA members recruited by HEWs under the health centers in the catchment areas of the intervention churches. An initial 5 day training will be given to priests and HDA members. The training will focus on newborn health topics including early initiation of and exclusive breastfeeding, maternal nutrition, immunization, childhood illnesses, child health care services, etc. At the end of the training action plans will be prepared by the training organizers, priests, and HDA. Priest will be asked to integrate health messages and education into their routine family visits around the birth of a child in structured intervals as culturally appropriate. The trained priests and HDA members will be dispatched to their respective communities to begin the intervention. Their primary activities will be identification of near-term pregnant and newly delivered women, providing health education to their families, follow-up visits to enable newborn-mother pairs to access child health care services, and to provide health education at religious and community gatherings. Specifically, pre-planned visits of parishioners' families will be done by the respective priests and the partnering HDA members during the last month of pregnancy, immediately after the delivery of the baby and around the time of baptism for the newborn. These visits will be used to educate pregnant and postpartum women and their families on newborn health topics including initiation of breastfeeding, duration of breastfeeding/ exclusive breastfeeding, vaccination, cord care, and utilization of available newborn health care services. These community based activities will be monitored through regular follow-up visits by the UoG study team and discussions with priests and HDA members. Newborn-mother pairs will be recruited within the first 10 days after delivery as reported to the study team by Health Extension Workers (HEWs) engaged in the study. Recruitment will start one month following the start of the intervention and all reported newborn-mother pairs who meet the screening criteria will be included in the study until the calculated sample sizes are reached. HEW's routine registers of new deliveries will be used to trace, recruit and screen study participants. Newborn-mother pairs who fulfill an initial screening criteria will be reported to the study team at the University of Gondar (UoG) who will travel to the study site regularly for recruitment of study participants and data collection. Newborn-mother pairs will be reported to the UoG study team both through phone calls made by HEWs and in-person at the time of regular onsite visits by the team. Newborn-mother pairs will be recruited within the first 10 days after delivery as reported to the study team by Health Extension Workers (HEWs) engaged in the study. Recruitment will start one month following the start of the intervention and all reported newborn-mother pairs who meet the screening criteria will be included in the study until the calculated sample sizes are reached. HEW's routine registers of new deliveries will be used to trace, recruit and screen study participants. Newborn-mother pairs who fulfill an initial screening criteria will be reported to the study team at the University of Gondar (UoG) who will travel to the study site regularly for recruitment of study participants and data collection. Newborn-mother pairs will be reported to the UoG study team both through phone calls made by HEWs and in-person at the time of regular onsite visits by the team. Eligible newborn-mother pairs will be visited by a member of the study team at their home or at an appointed meeting location in their community to complete the verbal informed consent process. Those pairs who attend church at a parish that received the intervention will be assigned to the intervention arm, and those from the parishes where no intervention was conducted will be assigned to the control arm. Initial baseline data will then be collected and follow-up visit schedules arranged with the study team.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Breastfeeding, Exclusive, Immunization; Infection, Growth; Stunting, Nutritional
Keywords
Community health worker

7. Study Design

Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
316 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Intervention
Arm Type
Experimental
Arm Title
Control
Arm Type
No Intervention
Intervention Type
Behavioral
Intervention Name(s)
Newborn Health Education
Intervention Description
Community influencers will receive training and give community education to women and their families regarding newborn health.
Primary Outcome Measure Information:
Title
Mid-upper arm circumference
Description
Anthropometric Measurement using MUAC tapes
Time Frame
Up to six months
Title
Proportion of mothers exclusive breastfeeding
Description
Self-reported breastfeeding behavior
Time Frame
Up to six months
Secondary Outcome Measure Information:
Title
Immunization status
Description
Collected from vaccination cards
Time Frame
Up to six months
Title
Frequency of acute illness
Description
Self reported
Time Frame
Up to six months
Title
Frequency of hospitalization status
Description
Self reported
Time Frame
Up to six months

10. Eligibility

Sex
Female
Minimum Age & Unit of Time
14 Years
Maximum Age & Unit of Time
49 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Newborn-mother pairs visited by the study staff (Enrolled women and newborns) The following inclusion criteria will be used during recruitment: Newborns should be those delivered at least one month after the start of the intervention period Newborn-mother pairs should be EOC parishioners Newborn's family should have a soul father (a spiritual advisor assigned to the family in the Ethiopian Orthodox tradition) Mother must have lived in the study area for at least 6 months Mothers must give written informed consent for themselves and their newborn Formative focus group discussion and key informant interview participants (FGD and KII participants) The following inclusion criteria will be used during recruitment: Mothers of newborns <6 months old Fathers of newborn children <6 months Ethiopian Orthodox priests from the North Gondar region Healthcare workers from government Health Centers (unit of primary care) All participants must have established residency in the region for >6 months All participant must give verbal informed consent Exclusion Criteria: Newborn-mother pairs visited by the study staff (Enrolled women and newborns) The following exclusion criteria will be used during recruitment: Newborns with gross developmental abnormalities that would make anthropometric measurements and interpretations difficult Newborns identified by the study team as in distress and in need of immediate, emergency care during the enrollment visit Newborn whose mother is not a member of an EOC parish Newborns whose mothers have died by the time of recruitment Newborn whose family plans to re-locate away from the study site in less than 6 months Newborns who were part of a multiple birth but are not the first born should be excluded Formative focus group discussion and key informant interview participants (FGD and KII participants) The following exclusion criteria will be used during recruitment: - Newly established residence in the Woreda (<6 months)
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Brandon Guthrie, PhD
Organizational Affiliation
University of Washington
Official's Role
Principal Investigator
Facility Information:
Facility Name
University of Gondar
City
Gondar
State/Province
Amhara
ZIP/Postal Code
P.O. Box 126
Country
Ethiopia

12. IPD Sharing Statement

Plan to Share IPD
Undecided

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Leading Advancements in the Uptake of Newborn Community Health

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