- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05836961
Impact of Benazir Nashonuma Program (BNP) on Maternal and Child Nutritional Status
Evaluating Effectiveness of Benazir Nashonuma Program (BNP) on Maternal and Infant Outcomes: A Non-randomized Intervention Study in Sindh and Punjab
The purpose of this study is to evaluate the impact of Benazir Nashonuma Program (BNP) which includes specialized nutritious food (SNF) augmented with specific reproductive health interventions during pregnancy on proportion of low birthweight babies and stunting among children, in low income setting of Pakistan. The study aims to answer if:
- Utilization of Benazir Nashonuma Program (BNP) among pregnant women is effective in reducing the proportion of low birthweight babies, compared to pregnant women who are not utilizing the program, among low income setting population.
- Utilization of Benazir Nashonuma Program (BNP) is effective in reducing the proportion of stunting among children, compared to those not utilizing the program, among low income setting population.
Participants who are enrolled in the Benazir Nashonuma Program (receiving intervention) and those who are not enrolled (not receiving intervention) will be followed throughout pregnancy till delivery. After delivery mother-baby dyad will be followed for a period of 12 months. Compliance of supplementation will be measured, and outcomes (low birthweight and stunting) observed throughout the follow up.
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Malnutrition in Pakistan is a major and pervasive public health issue. Every four under five children in our country are reported to be stunted, with a mighty prevalence of 40.2% stunting as reported in the National Nutritional Survey of Pakistan 2018. Pakistan also shares one of the highest burden of low birthweight (LBW) where 19% babies in urban and 32% in rural are born with weight <2500 grams. LBW babies have a higher risk of death compared to full term babies and contributes to 60-80% of all neonatal deaths.
The first 1000 days of life, the time from conception to 2 years of age, is a critical period, providing a window of opportunity for interventions to improve maternal and child nutrition and health outcomes including stunting and other nutritional markers. Availability and access to primary healthcare and nutrition services during pregnancy and the first two years of life can help prevent undernutrition and reduce infections in early life, helping reduce maternal and infant mortality, and preventing the lifelong and intergenerational consequences of malnutrition. Evidence-based nutrition interventions, especially the combination of BEP and small quantity lipid nutrient supplements have been shown to be effective in improving birth outcomes and reducing child stunting.
BNP is a health and nutrition CCT programme, with the aim to address stunting in children under 23 months of age. The CCT and Specialized Nutritious Food (SNF) are provided to Benazir Income Support Programme (BISP) participating women during pregnancy and lactation up to 6 months and to children aged 6-23 months contingent on their participation in and adherence to BNP interventions. In addition to the programme components, the pre-existing standard of care interventions including antenatal and postnatal care, childhood immunizations, growth monitoring and behavior change communication (BCC) activities, i.e., awareness sessions on health, nutrition and hygiene.
The primary study objectives are to assess the impact of intervention (BNP) on:
- Proportion of babies born with low birthweight.
- Prevalence of stunting among infants at 6 and 12 months of age
The secondary objectives related to maternal outcomes are to assess the impact of intervention on:
- Dietary diversity of women
- Mean nutrient intake including energy in kilo calories.
- Prevalence of iron deficiency anemia among lactating women.
- Proportion of pregnant women using reproductive health services.
The secondary objectives related to newborn and infant outcomes are to assess the impact of the intervention on:
- Prevalence of wasting among infants at 6 and 12 months of age.
- Incidence of anemia among infants at 6- and 12-months of age
- Infant and child feeding practices among infants at 6 and 12 months of age.
- Neurodevelopmental outcomes (cognitive, language and motor development) using Bayley Scales of Infant and Toddler Development (BSID-IV) at 6 months, and 12 months of age among children.
Other objectives include following:
- To measure receipt and utilization of BEP supplementation among pregnant and lactating women enrolled in BNP.
- To measure receipt and utilization on BEP supplementation among children under 12 months of age enrolled in BNP
- Household food insecurity status (using the Food Insecurity Experience Scale).
Study Type
Enrollment (Anticipated)
Phase
- Not Applicable
Contacts and Locations
Study Contact
- Name: Dr Sajid Bashir Soofi
- Phone Number: +923002769398
- Email: sajid.soofi@aku.edu
Study Contact Backup
- Name: Dr Asma Abdul Malik
- Phone Number: +923311388051
- Email: asma.qureshi@aku.edu
Study Locations
-
-
Sindh
-
Dadu, Sindh, Pakistan
- Recruiting
- Aga Khan Office
-
Contact:
- Asma Abdul Malik, MSc Epidemiology
- Phone Number: 00923311388051
- Email: asma.qureshi@aku.edu
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
Intervention arm: All pregnant women in their first or second trimester, who are enrolled in Benazir Nashonuma Program (BNP).
Non-intervention arm: All pregnant women in their first or second trimester, who are not enrolled in Benazir Nashonuma Program (BNP).
Exclusion Criteria:
- Women who intend to migrate or relocate for more than 3 months during the study period will be excluded from the study.
- Women in the non intervention group who are consuming specialized nutritious food (SNF) from any source at the time of enrollment will be excluded from the study.
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Prevention
- Allocation: Non-Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Experimental: BNP enrolled
Pregnant women in their first or second trimester who have been enrolled in BNP
|
Dietary supplement for pregnant women and lactating mothers during the first six months of lactation: Maamta is a 75-gram sachet made from peanut butter with 400 kcal of energy Dietary supplement for children aged 6-23 months: Wawamum is a lipid-based nutrient supplement consisting of skimmed milk powder, micronutrients, vegetable oil, roasted chickpeas and antioxidants. Wawamum covers the recommended daily dose of most micronutrients and 255 kcal of energy (1/4 of daily energy requirements for children in this age range) Conditional Cash Transfers (CCT): This includes stipends of PKR 2000 during pregnancy contingent on three antenatal care visits, consuming SNF, attending awareness sessions on health and nutrition, getting two doses of tetanus toxoid and institutional delivery. After delivery PKR 2000/- for boys and 2500/- for girls are paid as incentives conditioned on getting child's birth registered, routine immunization and consumption of SNF by the child from 6-23 months |
No Intervention: BNP non-enrolled
Pregnant women in their first or second trimester who are not enrolled in BNP
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Prevalence of low birthweight
Time Frame: Within 48-hours of delivery
|
Birth weight of less than 2500 g (up to and including 2499 g) within 48 hours of delivery
|
Within 48-hours of delivery
|
Prevalence of stunting
Time Frame: At 6 months of age
|
Height-for-age ≤-2 SD of the WHO Child growth standards median
|
At 6 months of age
|
Prevalence of stunting
Time Frame: At 12 months of age
|
Height-for-age ≤-2 SD of the WHO Child growth standards median
|
At 12 months of age
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Prevalence of wasting
Time Frame: At 6 and 12 months of age
|
Weight-for-height ≤-2 SD of the WHO Child growth standards median.
|
At 6 and 12 months of age
|
Prevalence of Iron deficiency anemia in pregnant women
Time Frame: At 9th month on pregnancy
|
Hemoglobin levels below 11 g/dl, serum ferritin less than or equal to 30 ng/ml, mean corpuscular volume MCV below 95 fl will be considered diagnostic of iron deficiency anemia
|
At 9th month on pregnancy
|
Prevalence of Iron deficiency anemia in infants
Time Frame: 2 point times: At 6 and 12 months of age
|
Hemoglobin concentration of less than 11.0 g/dl and ferritin levels of less than 15 micrograms/L
|
2 point times: At 6 and 12 months of age
|
Number of antenatal care (ANC) visits during pregnancy
Time Frame: At delivery
|
Attending at least 8 ANC consultations in a health facility/clinic
|
At delivery
|
Number of women who had an Institutional delivery
Time Frame: At delivery
|
Having delivered in a health facility
|
At delivery
|
Number of women who had Skilled birth attendance
Time Frame: At delivery
|
Birth attended by a skilled health personnel
|
At delivery
|
Number of women who had Postnatal care (PNC) check ups
Time Frame: 3 months after delivery
|
Receiving a postnatal health check while in a facility or at home within 6-weeks of postnatal period
|
3 months after delivery
|
Mean nutrient intake of energy in kilocalories of the pregnant woman
Time Frame: At 9th month of pregnancy
|
Mean nutrient intake of energy in kilocalories using 24-hour recall.
|
At 9th month of pregnancy
|
Prevalence of infants who were ever breastfed
Time Frame: At 12 months of age
|
Number of infants who were breastfed at least once
|
At 12 months of age
|
Prevalence of infants who had early initiation of breastfeeding
Time Frame: At 12 months of age
|
Number of infants who were put to the breast within one hour of birth
|
At 12 months of age
|
Prevalence of infants who were exclusively breastfed
Time Frame: At 12 months of age
|
Number of of infants aged 0-5 months who were fed exclusively with breast milk during the previous day
|
At 12 months of age
|
Prevalence of infants who consumed a minimum acceptable diet
Time Frame: At 12 months of age
|
Number of infants 6-12 months of age who consumed a minimum acceptable diet during the previous day
|
At 12 months of age
|
Prevalence of infants with minimum dietary diversity
Time Frame: At 12 months of age
|
Number of infants 6-12 months of age who consumed foods and beverages from at least four out of eight defined food groups during the previous day
|
At 12 months of age
|
Mean scores of Neurodevelopmental outcomes of the infant
Time Frame: At 12 months of age
|
Neurodevelopmental outcomes of the children will be assessed using Bayley Scales of Infant and Toddler Development (BSID-IV).
Mean scores will be reported for cognitive, language and motor development of the infant using Bayley's scales.
Higher scores in the Bayley Scales indicate better outcomes
|
At 12 months of age
|
Number of women consuming specialized nutritious food (SNF)
Time Frame: At 6 months after delivery
|
Utilization of supplementation (SNF) by the woman during pregnancy and first 6 months of lactation after delivery
|
At 6 months after delivery
|
Number of infants consuming specialized nutritious food (SNF)
Time Frame: At 12 months of age
|
Utilization of supplementation (SNF) by the infant from 6-23 months of age
|
At 12 months of age
|
Collaborators and Investigators
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Anticipated)
Study Completion (Anticipated)
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
Additional Relevant MeSH Terms
Other Study ID Numbers
- BNP Study
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.
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