Home Based Phototherapy for Neonatal Jaundice
Primary Purpose
Neonatal Jaundice
Status
Recruiting
Phase
Not Applicable
Locations
Bangladesh
Study Type
Interventional
Intervention
Home based phototherapy and referral
Sponsored by
About this trial
This is an interventional treatment trial for Neonatal Jaundice
Eligibility Criteria
Inclusion Criteria:
- The mothers are at late 2nd or early 3rd trimester of their pregnancy and agreed to enroll as study participants
- They are planning to stay in the study village for the next 12 months (if a mother is planning to give birth at her natal home and then return, she will still not be a candidate for enrollment)
Exclusion Criteria:
- Pregnant mother with confirmed multiple pregnancy.
- Pregnant mother with medically identified psychological disorder.
- Any known maternal danger sign.
Sites / Locations
- MirzapurRecruiting
Arms of the Study
Arm 1
Arm 2
Arm Type
Active Comparator
No Intervention
Arm Label
Intervention
Control
Arm Description
Educational session of pregnant mothers, blood grouping of parents and identifying risk factors for developing jaundice, screening newborns for neonatal jaundice, glucose 6-phosphate dehydrogenase deficiency and illness, Home based phototherapy and referral.
No intervention will be deliver
Outcomes
Primary Outcome Measures
Breastfeeding rates within 1 hour of age
Mother reported breastfeeding rates within 1 hour of age will be measured following structured survey
Breastfeeding rates upto 3 months of age
Mother reported breastfeeding rates after 3 months of age will be measured following structured survey
Number of newborns having at least one postnatal check-up within 48 hours.
This measurement will be taken within 2 months of child birth through a structured survey, reported by mother.
Number of newborns screened for neonatal jaundice
Number of newborns screened for neonatal jaundice either in home or any government or non-government health facilities within 7 days of birth through a structured survey reported by mother.
Number of newborns that received indicated treatment for neonatal jaundice
Number of children receiving indicated treatment for neonatal jaundice either in home or health facilities will be measured by a mother reported structured survey after 2 months of child birth
Community health workers (CHW's) skill in assessing sick newborns
CHW's skill will be measured through a structured observation following a check list and subjective and objective assessment by registered physician
Secondary Outcome Measures
Full Information
NCT ID
NCT03933423
First Posted
April 23, 2019
Last Updated
March 29, 2022
Sponsor
International Centre for Diarrhoeal Disease Research, Bangladesh
Collaborators
Stanford University, Dhaka Shishu Hospital
1. Study Identification
Unique Protocol Identification Number
NCT03933423
Brief Title
Home Based Phototherapy for Neonatal Jaundice
Official Title
Using Community Health Workers and In-home LED Phototherapy to Dramatically Reduce Brain Damage From Neonatal Jaundice in Low to Middle Income Countries: A Feasibility Trial
Study Type
Interventional
2. Study Status
Record Verification Date
March 2022
Overall Recruitment Status
Recruiting
Study Start Date
May 1, 2019 (Actual)
Primary Completion Date
December 2022 (Anticipated)
Study Completion Date
December 2022 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
International Centre for Diarrhoeal Disease Research, Bangladesh
Collaborators
Stanford University, Dhaka Shishu Hospital
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 main purpose of the study is to deliver community health worker based prevention, early screening and management of neonatal Jaundice using battery powered LED phototherapy device at the household level.
Detailed Description
Bangladesh like other low and middle-income countries has a high burden of hyperbilirubinemia induced neonatal morbidity and mortality. Approximately 60%-80% of newborns develop neonatal jaundice and 18% of infants are at risk for adverse outcomes from neonatal jaundice. Severe neonatal jaundice can put neonates at risk for long term neuro-developmental impairments and death. Delay in diagnosis and treatment of severe neonatal jaundice can result in brain damage to the newborn that is preventable with timely treatment.
Approximately 14 million infants per year in low to middle-income countries (LMIC) are at risk from neonatal jaundice progressing to extreme hyperbilirubinemia and brain damage. Nearly 80% of the 481,000 cases of extreme hyperbilirubinemia are in LMIC because infants are identified too late or health facility treatment is inaccessible or inadequate.
New, low-cost, easy to use screening and phototherapy treatment technologies enable our proposed redesign of care delivery in LMIC to save infant's brains. The investigators plan to shift care from specialists and hospitals to community health workers (CHW) and homes. Investigators will integrate CHW-led prevention during pregnancy, with timely household screening and treatment. Investigators will reach infants before brain damage occurs and treat infants who would not otherwise be treated.
LMIC including Bangladesh have had difficulty addressing neonatal jaundice because of the expense and logistics of providing timely prevention, screening and treatment to families. This study aim to test 3 hypothesis:
H1: Prenatal modules for pregnant mothers will increase breastfeeding rates at 1 hour of life and at 3 months of age.
H2: CHWs can screen 80% of newborns by 48 hours of age for jaundice and are skilled in identifying sick infants.
H3: CHW-led household screening for neonatal jaundice will increase the rate of indicated treatment for neonatal jaundice compared to current practice.
Investigators will conduct formative research to engage Government and other stakeholders to develop intervention package for prevention and treatment of neonatal jaundice and configuring and adapting LED phototherapy device to use for home treatment. Investigators will then conduct randomized control trial to implement the intervention package in intervention community and will assess the effectiveness of the intervention package. Investigators will compare the rates of indicated treatment for neonatal jaundice in the intervention and treatment arms.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Neonatal Jaundice
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
500 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
Intervention
Arm Type
Active Comparator
Arm Description
Educational session of pregnant mothers, blood grouping of parents and identifying risk factors for developing jaundice, screening newborns for neonatal jaundice, glucose 6-phosphate dehydrogenase deficiency and illness, Home based phototherapy and referral.
Arm Title
Control
Arm Type
No Intervention
Arm Description
No intervention will be deliver
Intervention Type
Device
Intervention Name(s)
Home based phototherapy and referral
Other Intervention Name(s)
Educational session, identifying risk factors and, screening
Intervention Description
CHWs will visit the household twice in a month and will counsel mother and families on use of preventive care such as routine antenatal check care and newborn care. The investigators will conduct blood grouping and rhesus (Rh) typing. If the mother is Rh negative, investigators will also measure the Rh status of the father prior to delivery to determine the risk of Rh disease in the newborn. The investigators will establish an emergency contact system both in intervention and comparison arm where mothers and family members contact and inform the research team about delivery. The trained phlebotomist will collect cord blood for measuring glucose 6-phosphate dehydrogenase and infant blood type, Rh status, direct antigen testing. The investigators will develop a protocol for treating infants at home based on the ETAT (Emergency Triage Assessment AND Treatment) AAP (American Academy of Paediatrics) guidelines and treat with LED based phototherapy
Primary Outcome Measure Information:
Title
Breastfeeding rates within 1 hour of age
Description
Mother reported breastfeeding rates within 1 hour of age will be measured following structured survey
Time Frame
6-8 months after the intervention
Title
Breastfeeding rates upto 3 months of age
Description
Mother reported breastfeeding rates after 3 months of age will be measured following structured survey
Time Frame
6-8 months after the intervention
Title
Number of newborns having at least one postnatal check-up within 48 hours.
Description
This measurement will be taken within 2 months of child birth through a structured survey, reported by mother.
Time Frame
6-8 months after the intervention
Title
Number of newborns screened for neonatal jaundice
Description
Number of newborns screened for neonatal jaundice either in home or any government or non-government health facilities within 7 days of birth through a structured survey reported by mother.
Time Frame
6-8 months after the intervention
Title
Number of newborns that received indicated treatment for neonatal jaundice
Description
Number of children receiving indicated treatment for neonatal jaundice either in home or health facilities will be measured by a mother reported structured survey after 2 months of child birth
Time Frame
6-8 months after the intervention
Title
Community health workers (CHW's) skill in assessing sick newborns
Description
CHW's skill will be measured through a structured observation following a check list and subjective and objective assessment by registered physician
Time Frame
During 6-8 months of the intervention
10. Eligibility
Sex
Female
Gender Based
Yes
Gender Eligibility Description
Pregnant mothers above 18 years
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
45 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria:
The mothers are at late 2nd or early 3rd trimester of their pregnancy and agreed to enroll as study participants
They are planning to stay in the study village for the next 12 months (if a mother is planning to give birth at her natal home and then return, she will still not be a candidate for enrollment)
Exclusion Criteria:
Pregnant mother with confirmed multiple pregnancy.
Pregnant mother with medically identified psychological disorder.
Any known maternal danger sign.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Md Mahbubur Rahman, MBBS
Phone
8802-9827001
Ext
4003
Email
mahbubr@icddrb.org
Facility Information:
Facility Name
Mirzapur
City
Tangail
State/Province
Dhaka
Country
Bangladesh
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Mahbubur Rahman, MD, MPH
Phone
01712001294
Email
mahbubr@icddrb.org
12. IPD Sharing Statement
Plan to Share IPD
Undecided
Citations:
PubMed Identifier
35459113
Citation
Jahan F, Foote E, Rahman M, Shoab AK, Parvez SM, Nasim MI, Hasan R, El Arifeen S, Billah SM, Sarker S, Hoque MM, Shahidullah M, Islam MS, Ashrafee S, Darmstadt GL. Evaluation of community health worker's performance at home-based newborn assessment supported by mHealth in rural Bangladesh. BMC Pediatr. 2022 Apr 22;22(1):218. doi: 10.1186/s12887-022-03282-6.
Results Reference
derived
Learn more about this trial
Home Based Phototherapy for Neonatal Jaundice
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