- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04798833
Newborn Care Kit to Save Lives in GB, Pakistan (iNCK)
An Integrated Newborn Care Kit to Save Newborn Lives and Improve Health Outcomes in Gilgit-Baltistan, Pakistan
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
While some progress has been made towards reducing global under-5 mortality, in 2019, an estimated 2.4 million newborn deaths still occurred worldwide, accounting for 47% of all under-five deaths. Most neonatal deaths are caused by prematurity, sepsis, and intrapartum-related complications.
Pakistan has the highest neonatal mortality rate (NMR) in the world, at 42 deaths per 1,000 live births. Gilgit-Baltistan (GB), Pakistan's remote, northern-most administrative territory, is afflicted with some of the country's worst NMRs. High rates of home deliveries, low adoption of safe birth practices, inadequate cord care, and high maternal mortality contribute to this health disparity. GB's geography, climate, and underdeveloped infrastructure also largely restrict access to health care facilities. Health care at the community level in Pakistan is primarily supported by the Lady Health Worker (LHW) Programme. LHWs form a cadre of government-supported community health workers who provide newborn and maternal health services in GB. However, each of these health care workers is responsible for approximately 1,000 people, which restricts both availability and comprehensiveness of care, particularly for families that live in hard to reach areas.
Many proven, cost-effective ways to save newborn lives and improve wellbeing exist; however, they are not always available to those who need them most, nor are they packaged into a single portable kit that can be used in the home. An easy-to-use kit consisting of low cost, evidence-based interventions has potential to improve health status, reduce NMR, and provide more timely access to health services in remote areas such as GB. Between April 2014 and August 2015, the investigators conducted a community-based, cluster randomized intervention trial examining the effectiveness of delivering an integrated newborn care kit (iNCK) to pregnant women in Rahim Yar Khan (RYK), Punjab, Pakistan. The iNCKs were delivered by LHWs, who also educated participants how to use the different kit components. Neonatal mortality and morbidity outcomes were compared between iNCK recipients and a local control group who received the same standard of care, but no iNCK. The investigators found that while distribution of the iNCK did not significantly reduce neonatal mortality, utilization of the iNCK significantly reduced the risk of omphalitis and fever. Moreover, using the LHW network to distribute the intervention proved a feasible delivery mechanism.
The findings from the RYK trial suggest that while a network of community health workers can reliably deliver integrated interventions to pregnant women, further investigation is needed to improve the integration of educational content and maximize the iNCK's potential health benefits. Moreover, effective delivery of maternal health interventions through the iNCK warrants examination, as Pakistan experiences some of the world's highest rates of maternal mortality, of which post-partum hemorrhage (PPH) is a leading cause.
Study Type
Enrollment (Estimated)
Phase
- Not Applicable
Contacts and Locations
Study Contact
- Name: Shaun Morris, MD, MPH
- Phone Number: 416-813-7500 extension: 206625
- Email: shaun.morris@sickkids.ca
Study Locations
-
-
-
Islamabad, Pakistan
- Recruiting
- Aga Khan Health Services, Pakistan
-
Contact:
- Sher Hafiz
- Phone Number: +92 3469547314
- Email: sher.hafiz@akhsp.org
-
Karachi, Pakistan
- Active, not recruiting
- Aga Khan University
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Child
- Adult
- Older Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- Resides in a village with LHW coverage in participating union councils (clusters) in Astore, Diamer, Shigar, Ghanche, Kharmang, and Skardu, districts of GB, Pakistan
- In their 3rd trimester of pregnancy (≥ week 27 gestational age)
- Intends to be present in the study catchment area between day 29 and 35 postnatal age
- Provides written informed consent or assent
Exclusion Criteria:
- Does not reside within the study's catchment area at the time of enrolment
- Plans to relocate outside of the study catchment area within one month after the delivery of their newborn(s) and not return to the study catchment area
- Does not provide written informed consent or assent
- Lives in a village without LHW coverage
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Prevention
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Experimental: Integrated Newborn Care Kit
The integrated newborn care kit will contain a clean birth kit to be used at the time of delivery either at home or in a facility, three misoprostol tablets (200ug each), 4% chlorhexidine solution, sunflower oil emollient, temperature monitoring strip or sticker, a fleece blanket, a reusable, non-electric, heating device, and a pictorial instruction guide. Lady Health Workers will be equipped with a hand-held electronic scale to identify low birth weight newborns. Participants in this arm will receive the same local standard of care as the no intervention arm. |
Contents of the integrated newborn care kit:
Other Names: Neonatal Care Kit
Other Names:
|
No Intervention: Control (Local Standard of Care)
In the control arm, LHWs will deliver the local standard of care, which entails both anti-natal and post-natal LHW home visits. As part of standard practice, LHWs visit pregnant women in their homes during the 3rd trimester, at which time these health workers:
These community health workers will identify early danger signs in newborns such as infections and teach caregivers to identify the same symptoms, so that early interventions can be made. If danger signs are identified, the LHW will refer newborns to the appropriate level of health care. |
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
All-cause neonatal mortality
Time Frame: Day 29 postnatal age
|
Death from any cause within the first 28 days of life
|
Day 29 postnatal age
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Cumulative incidence of omphalitis
Time Frame: Day 29 postnatal age
|
Cumulative incidence of omphalitis among neonates where omphalitis is defined as:
|
Day 29 postnatal age
|
Cumulative incidence of post-partum hemorrhage (PPH)
Time Frame: Day 29 postnatal age
|
Cumulative incidence of PPH is self-reported. PPH is defined as having experienced any of the following:
|
Day 29 postnatal age
|
Health facility utilization
Time Frame: Day 29 postnatal age
|
Self-reported health facility utilization by pregnant women, and/or neonates and mothers in the first month post-partum
|
Day 29 postnatal age
|
Cumulative incidence of hypothermia among participants in the experimental arm
Time Frame: Day 29 postnatal age
|
Cumulative incidence of hypothermia defined by color change in temperature monitoring strip or sticker that indicates lower than normal temperature
|
Day 29 postnatal age
|
Cumulative incidence of fever among participants in the experimental arm
Time Frame: Day 29 postnatal age
|
Cumulative incidence of fever defined by color change in temperature monitoring strip or sticker that indicates higher than normal temperature
|
Day 29 postnatal age
|
Correlates of iNCK instructional compliance
Time Frame: Day 29 postnatal age
|
Correlates of iNCK instructional compliance, using a process analysis to explore the correlation between compliance and maternal, infant, sociodemographic characteristics, and Lady Health Worker teaching quality
|
Day 29 postnatal age
|
Correlates of willingness to pay for the iNCK
Time Frame: 29 postnatal age
|
Explore the correlation between maternal, infant, and sociodemographic characteristics, and knowledge, attitudes, practice, and willingness to pay for the iNCK
|
29 postnatal age
|
Cause-specific neonatal mortality
Time Frame: Day 29 postnatal age
|
Death from specific causes within the first 28 days of life
|
Day 29 postnatal age
|
Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Shaun Morris, MD, MPH, The Hospital for Sick Children
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Estimated)
Study Completion (Estimated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- TTS181021048
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
product manufactured in and exported from the U.S.
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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