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CTRI Number  CTRI/2014/12/005282 [Registered on: 11/12/2014] Trial Registered Prospectively
Last Modified On: 28/10/2017
Post Graduate Thesis  No 
Type of Trial  Interventional 
Type of Study   Preventive
Behavioral 
Study Design  Cluster Randomized Trial 
Public Title of Study   Can an intervention involving improvements in community-based newborn massage practice with promotion of cold-pressed sunflower oil as preferred emollient improve newborn survival in rural North India? 
Scientific Title of Study   Impact of topical application of cold-pressed sunflower seed oil with improved massage practices on neonatal mortality: a cluster randomized controlled trial in rural North India 
Trial Acronym   
Secondary IDs if Any  
Secondary ID  Identifier 
ISRCTN38965585  ISRCTN 
 
Details of Principal Investigator or overall Trial Coordinator (multi-center study)  
Name  Dr Vishwajeet Kumar 
Designation  Principal Investigator 
Affiliation  Community Empowerment Lab 
Address  Community Empowerment Lab. 26/11, Wazir Hasan Road Lucknow. 226001 Uttar Pradesh.

Lucknow
UTTAR PRADESH
226001
India 
Phone  0522-4932314  
Fax  0522-4932309  
Email  vishwajeet.kumar@shivgarh.org  
 
Details of Contact Person
Scientific Query
 
Name  Dr Vishwajeet Kumar 
Designation  Principal Investigator 
Affiliation  Community Empowerment Lab 
Address  Community Empowerment Lab. 26/11, Wazir Hasan Road Lucknow. 226001 Uttar Pradesh.

Lucknow
UTTAR PRADESH
226001
India 
Phone  0522-4932314  
Fax  0522-4932309  
Email  vishwajeet.kumar@shivgarh.org  
 
Details of Contact Person
Public Query
 
Name  Dr Vishwajeet Kumar 
Designation  Principal Investigator 
Affiliation  Community Empowerment Lab 
Address  Community Empowerment Lab. 26/11, Wazir Hasan Road Lucknow. 226001 Uttar Pradesh.

Lucknow
UTTAR PRADESH
226001
India 
Phone  0522-4932314  
Fax  0522-4932309  
Email  vishwajeet.kumar@shivgarh.org  
 
Source of Monetary or Material Support  
Department of Maternal Newborn Child and Adolescent Health World Health Organization 
 
Primary Sponsor  
Name  Department of Maternal Newborn Child and Adolescent Health World Health Organization 
Address  World Health Organization Avenue Appia 20 1211 Geneva 27 Switzerland Geneva 1211 Switzerland 
Type of Sponsor  Other [Inter-governmental organization] 
 
Details of Secondary Sponsor  
Name  Address 
NA  N/A 
 
Countries of Recruitment     India  
Sites of Study  
No of Sites = 1  
Name of Principal Investigator  Name of Site  Site Address  Phone/Fax/Email 
Dr Vishwajeet Kumar  Shivgarh  Saksham, Room No. 1, First floor Mahesh Vilas, Shivgarh, Rae Bareli, Uttar Pradesh. India, 229308
Rae Bareli
UTTAR PRADESH 
0522-4932314
0522-4932309
vishwajeet.kumar@shivgarh.org 
 
Details of Ethics Committee  
No of Ethics Committees= 2  
Name of Committee  Approval Status 
Community Empowerment Lab Institutional Ethics Committee (CEL IEC)  Approved 
World Health Organization Research Ethics Review Committee (WHO ERC)  Approved 
 
Regulatory Clearance Status from DCGI  
Status 
Not Applicable 
 
Health Condition / Problems Studied  
Health Type  Condition 
Healthy Human Volunteers  Newborn Sepsis, Prematurity, Newborn skin care, Newborn massage, Neonatal mortality rate reduction, community-based newborn care 
 
Intervention / Comparator Agent  
Type  Name  Details 
Intervention  Cold pressed sunflower seed oil (SSO) with improved newborn massage practices  The technical intervention essentially consists of: (a) the product, i.e. cold-pressed sunflower seed oil, and (b) accompanying directions for newborn massage. The “directions for newborn massage” further consist of the following aspects: i. Dosage of SSO, comprising of frequency of use, quantity per use, and duration of use. o Dose: 10g per application, applied 3x daily o Duration: 0-27 days of life ii. Improvements in overall massage practice: o Encourage hand washing prior to massage o Encourage gently massaging the vernix into the newborn skin, rather than forcefully removing it o Promote gentle massage of newborns o Delay use of mustard oil and skin-scrubbing substances such as bukwa (coarse-grained paste made of mustard/wheat seeds along with additives) past the newborn period o Ensure that the newborn is kept warm during and after massage Pregnant women who intend to deliver in the intervention area and consent to participate in the trial would be oriented to the intervention and provided an initial supply of oil at 24-27 weeks of gestation, in order to ensure early application on preterm newborns. After birth, oil supply will be replenished on a regular basis by logistics officers. All traditional massage providers (called ‘nauns’) providing services in the intervention area would be trained in improved massage practice, and will be expected to train mothers and care providers in the recommended practice.  
Comparator Agent  Current traditional newborn massage practices in the community  No intervention will be introduced in the control group, which will continue following the same traditional massage practices, including the type of oil used.  
 
Inclusion Criteria  
Age From  0.00 Day(s)
Age To  27.00 Day(s)
Gender  Both 
Details  All newborns (or neonatal deaths) identified in the study area till 7 days of delivery irrespective of place of delivery will be considered as eligible for analysis of trial outcomes. The inclusion criteria would be met in the community, in the following conditions:
1. mother stays through the antenatal period and delivers in the study village
2. mother delivers outside the study village (e.g., maternal home or health facility) but returns to the study village within the first 7 days of delivery.
3. In case of maternal deaths, newborns identified in the study villages within 7 days of delivery.
Thus, all women/babies who are found to be residing in a particular cluster at the time of first identification during the first 7 days of delivery will be analyzed as part of the same cluster, irrespective of migration or place of delivery, as per principles of intention to treat.  
 
ExclusionCriteria 
Details  None. All babies fulfilling the inclusion criteria will be included in the study. 
 
Method of Generating Random Sequence   Computer generated randomization 
Method of Concealment   Not Applicable 
Blinding/Masking   Not Applicable 
Primary Outcome  
Outcome  TimePoints 
1. NMR post-24 hours of birth or the number of neonatal deaths that occur after 24 hours of birth, per 1000 live births.

2. Neonatal mortality rate (NMR) or the number of neonatal deaths per 1000 live births
 
Day 1 and Day 28 
 
Secondary Outcome  
Outcome  TimePoints 
1. Infections and hospitalization
2. Growth of the newborn
3. Skin barrier function and skin scoring
4. Dose – response relationship
5. Intervention coverage
6. Changes in practices
7. Adherence to Intervention
 
Day 0, 1, 3, 7, 28 
 
Target Sample Size   Total Sample Size="41072"
Sample Size from India="41072" 
Final Enrollment numbers achieved (Total)= "27570"
Final Enrollment numbers achieved (India)="27570" 
Phase of Trial   N/A 
Date of First Enrollment (India)   01/01/2015 
Date of Study Completion (India) 22/11/2016 
Date of First Enrollment (Global)  Date Missing 
Date of Study Completion (Global) Date Missing 
Estimated Duration of Trial   Years="2"
Months="0"
Days="0" 
Recruitment Status of Trial (Global)
Modification(s)  
Not Applicable 
Recruitment Status of Trial (India)  Completed 
Publication Details   No publications yet 
Individual Participant Data (IPD) Sharing Statement

Will individual participant data (IPD) be shared publicly (including data dictionaries)?  

Brief Summary  

Serious infections and complications of preterm birth together contribute to almost 60% of newborn deaths worldwide. The human skin is a very important organ and serves as an important barrier to infection. The skin barrier of the newborn, and especially preterm babies has fewer layers and is not fully functionally mature. However, communities across the north Indian belt, Nepal and Bangladesh have several practices that may further compromise the skin barrier and expose newborns to a higher risk of infection. These include forceful removal of the vernix (a protective greasy substance that covers the baby’s skin when born) often with coarse substances that can further abrade the skin, regular massage of babies with flour/ mustard seed paste (which can be abrasive to newborn skin) from the first day itself, massaging with mustard oil which is known to delay skin barrier recovery, putting oil into body orifices, etc. The proposed intervention consists of promoting cold-pressed sunflower seed oil sunflower seed oil, that has been shown to improve skin condition, accelerate recovery of the skin barrier function and reduce the risk of infections and death among hospitalized newborns in low-resource settings, for massage of newborns, alongwith improved and hygienic massaging practices. The aim of the study is to assess the impact of topical application of cold-pressed SSO with improved massage practices, as compared to standard community-based massage practices, on neonatal mortality.

 

The study has been designed as a public health efficacy trial, and will be evaluated using a 2-arm cluster randomized controlled design in 276 contiguous villages (clusters) in rural Uttar Pradesh, India. All the newborns identified in the study area within 7 days of delivery will be included in the study. For the purpose of enrollment, pregnant women will be identified within 24 weeks of gestation, and prospectively followed until 28 days of delivery. The study will enroll approximately 42,000 newborns over a period of 24 months, beginning January 2015.

 

In the intervention arm, we will train women who traditionally massage newborns during the first 10-12 days of life (called nauns) in the improved and hygienic massage technique. Cold-pressed sunflower oil will be distributed to all mothers in the intervention arm with instructions on its application to newborn babies. The nauns are also expected to train mothers and families in the improved massage technique. No such intervention will be introduced in the control group, which will continue following the same traditional massage practices.

 

The study will track vital events (pregnancies, births, newborn deaths) in the entire study area through a prospective follow-up of all mothers until 28 days of delivery and measure other key outcomes. Newborn deaths in the intervention and control groups will be statistically compared, along with changes in practices and other key outcome indicators to evaluate the impact of the intervention.

 

Risks & potential benefits: The activities in the intervention arm are expected to cause no harm to babies and may potentially reduce the incidence of newborn infections and deaths. Sunflower oil is a natural oil that is safe for massage and has been used previously in hospital based studies. Mothers and caregivers will be trained by nauns (community masseuses) in the practice of improved and hygienic massage that will mitigate risk to the newborn’s skin barrier function. There is no additional risk to infants in the control arm, who will continue to receive traditional newborn massage as practiced by families. The evaluation procedures are standard, and include measuring parameters such as weight and temperature of the baby. Mothers will be asked detailed questionnaires regarding massage practices, other newborn care practices, illnesses, care-seeking, etc. These involve minimal risk to participants.

 

The study is supported by the World Health Organization, Geneva, through a grant from the Bill & Melinda Gates Foundation. The primary contact for the study is the Principal Investigator, Dr. Vishwajeet Kumar (vishwajeet.kumar@cel.org.in).

 
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