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Impact of School Milk Program on Nutritional Status of Primary School Children

Impact of School Milk Program on Nutritional, Body Composition and School Performance of Primary School Children in Attock and Sheikhupura

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05493449
Enrollment
7799
Registered
2022-08-09
Start date
2021-12-01
Completion date
2022-12-16
Last updated
2023-03-06

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Milk Intervention on Body Composition and School Attendance

Brief summary

Malnutrition is very common in Pakistan, especially in children of under developed areas due to lack of resources and access to nutritious food. It can disturb the normal physical and mental development as well as functioning in children which can put economic burden on country level. Therefore, school meal programs can play an important role in providing school children with healthy and nutritious food which can improve their nutritional status as well as overall health.

Detailed description

The proposed intervention study was conducted in the primary school going children of age 4-16 years old in two districts of Punjab namely Attock and Sheikhpura with collaboration of University of Veterinary and Animal Sciences, Lahore, University of Education, Lahore and Friesland Campina (Engro Foods Pvt. Ltd.), Pakistan. The participants of study was students studying in classes nursery to 5, out of study population of 90 Schools of different tehsils of two districts (Attock city and Sheikupura city), Punjab-Pakistan that are being run by the administration of University of Education, Lahore. The study participants for research are 8.9 % of 7799 total population involved in school milk program children i.e. total 693 (380 Attock city and 313 Sheikhupura). A total of 18 schools (9 from each district) was selected as a sample of the study population, since there were three groups (A-Group to receive Full Cream Milk; B-Group to receive Flavored Milk; C-Group is control) and three schools in each districts form each group. In addition, the selected schools have been selected in each district in a way in both selected districts to have a uniform population of around 160±5. At initiation of the study, baseline data was collected from the study participants. Data regarding socio-demographic factors, 24-hrs dietary recall, anthropometric, school attendance, body composition, dietary deficiency signs and symptoms was collected from study population i.e. 693 students. After baseline findings, for dietary intervention, the sample population based on schools was divided into 3 clusters/group including control, Ultra High Temperature (UHT) and flavored milk as intervention groups (i.e., UHT and flavored milk groups, were given milk (180 mL/participants/day; on alternate days basis and/or daily basis as the case may be owing to Covid situation) for 3 months. The data was collected from study participants at different intervals initiation (baseline) and termination (3 months), whereas, data after 2 months of termination will be collected to estimate washout period differences of the intervention on the study parameters. After the completion of study, the control group will also receive milk for same duration on humanitarian basis. Inclusion Criteria: Children having no symptoms of Lactose Intolerance Exclusion Criteria: Children having symptoms of Lactose Intolerance Informed Consent and other considerations: All the protocols of study were explained to study participants/teachers and informed consent was obtained prior to enrollment in the study. The data was considered as relevant and reliable, if 70% of the sample (compared to start of the study) completes the study with minimum of 80% of allocated milk consumption. If any student(s) wants to quit during the course of the study, he/she do it on his/her will and was not forced to complete the study. Data Analysis: Descriptive analysis was carried out by using SPSS version 25 (SPSS for windows version 25; SPSS Inc., Chicago, IL, USA), Microsoft excel and World Health Organization Anthroplus (Software) was used to calculate height for age and BMI for age z scores. The data was analyzed by using independent sample t-test, paired sample t-test and one-way ANOVA, statistical significance was at p \> 0.05.

Interventions

COMBINATION_PRODUCTUHT Milk

In this group of participants, UHT milk, 180 mL was provided and results were compared with control and flavored milk group

COMBINATION_PRODUCTFlavored Milk

In this group of participants, flavored milk, 180 mL was provided and results were compared with control and UHT group

Sponsors

University of Lahore
CollaboratorOTHER
Friesland campina Engro Pakistan
CollaboratorUNKNOWN
University of Veterinary and Animal Sciences, Lahore - Pakistan
Lead SponsorOTHER

Study design

Allocation
NON_RANDOMIZED
Intervention model
FACTORIAL
Primary purpose
OTHER
Masking
NONE

Masking description

No masking is involved as participants, investigator and assessor know intervention types

Intervention model description

There were three groups in study. Group A is the one which received UHT Milk, Group B received Flavored Milk and Group C was a control group.

Eligibility

Sex/Gender
ALL
Age
4 Years to 16 Years
Healthy volunteers
Yes

Inclusion criteria

• Participants aged 4-16 years of age enrolled under University of Education, Lahore who are having no symptoms of Lactose Intolerance

Exclusion criteria

• Participants having symptoms of Lactose Intolerance

Design outcomes

Primary

MeasureTime frameDescription
Waist to Hip ratio (WHR)change from baseline to 3 monthsWHR of the study participants was measured by using body composition analyzer Inbody J-270.
Inbody Scorechange from baseline to 3 monthsInbody Score of the study participants was measured by using body composition analyzer Inbody J-270.
Visceral Fat Level (VFL)change from baseline to 3 monthsVFL of the study participants was measured by using body composition analyzer Inbody J-270.
Body Fat Mass (BFM)change from baseline to 3 monthsBody fat mass of the study participants was measured by using body composition analyzer Inbody J-270.
Skeletal Muscle Mass (SMM)change from baseline to 3 monthsSMM of the study participants was measured by using body composition analyzer Inbody J-270.
Percentage Body Fat (PBF)change from baseline to 3 monthsPBF of the study participants was measured by using body composition analyzer Inbody J-270.
Weightchange from baseline to 3 monthsWeight of the study participants was measured by using weighing balance.
Heightchange from baseline to 3 monthsHeight of the study participants was measured by using stadiometer.
Total Body Water (TBW)change from baseline to 3 monthsTBW of the study participants was measured by using body composition analyzer Inbody J-270.
Body Proteinchange from baseline to 3 monthsBody protein of the study participants was measured by using body composition analyzer Inbody J-270.
Mineralschange from baseline to 3 monthsBody minerals of the study participants was measured by using body composition analyzer Inbody J-270.

Secondary

MeasureTime frameDescription
Nutritional deficiency Assessmentchange from baseline to 3 monthsThe study participants were examined physically to check nutritional deficiencies along with signs & symptoms including hair, mouth, lips, eyes, gums, teeth, tongue, face, skin, nails, musculoskeletal and neck etc. Deficiencies related to various macro and micronutrients were also examined i.e., energy, proteins, vitamin A, D, calcium, riboflavin, Vitamin B12 etc.
Attendance percentagechange from baseline to 3 monthsStudent attendance from school records was evaluated for documenting their involvement and performance.

Countries

Pakistan

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026