Serial Body Composition Measurements by PEAPOD (SBMP)

November 3, 2026 updated by: Shoklo Malaria Research Unit

Body Composition at Birth and Its Evolution Over the First 6 Months in Neonates Using Air-displacement Plethysmography (PEAPOD Machine): A Prospective Longitudinal Matched Case-control Study in a Low-income Setting

Birth weight alone is not precise enough to explain the nutritional status of a newborn baby. For SGA babies (born smaller than they should be for birth age and sex) a sophisticated machine called a PEAPOD can calculate the percentage of body fat, fat mass and fat-free mass. The PEAPOD does these measurements by moving air around a baby placed on a scale inside a Pod. The procedure is quick (average 7 minutes), accurate, safe and useful to 6 months of age. The investigators want to understand if there are clues in the body composition of babies born to small compared to babies of the right size that point to why born too small have increased risk of heart and blood vessel problems linked to issues like diabetes and obesity, later in life. A type of study called "matched case-control" could help us investigate mother factors that are associated with being born too small. Cases (SGA) will be matched with controls (AGA, a baby born not too small and not too large) based on sex, weeks of age at birth (±1 week), number of births the mother has had (same parity). Information about the study will be given in pregnancy. If consent is provided blood samples (mother and cord) will be collected at birth. Small amount of blood will be taken from mother and baby one time at birth, 1, 2, 3, 4, 5 and 6 months; and babies will attend for 7 PEAPOD measurements unless birth weight >6.0kg is reached first. Additionally, mother's breast milk will be collected. These will be used to measure different molecules in the blood related to health and disease. With the data from this study, the investigators may be able to provide better recommendations during pregnancy that can help optimize baby and infant nutritional status and adult health outcomes.

Study Overview

Detailed Description

This study aims to investigate body composition at birth and its evolution over the first six months of life in neonates using air-displacement plethysmography (PEAPOD). Traditional anthropometric measures such as birth weight and length provide limited information on neonatal nutritional status, as they do not distinguish between fat mass and fat-free mass. Understanding early body composition may offer important insights into infant growth patterns and long-term health outcomes, including risks of metabolic and cardiovascular diseases.

This is a prospective longitudinal matched case-control study conducted at the Mawker Thai Clinic, Shoklo Malaria Research Unit (SMRU), along the Thailand-Myanmar border. The study will recruit 300 mother-infant pairs, including 150 small-for-gestational-age (SGA) neonates and 150 appropriate-for-gestational-age (AGA) neonates. Cases and controls will be matched based on sex, gestational age (±1 week), and parity.

Following informed consent obtained during pregnancy, baseline maternal data will be collected from routine antenatal care. After delivery, neonatal eligibility will be confirmed, and study procedures will begin within 24-48 hours of birth. Body composition measurements will be performed using the PEAPOD device, a validated, non-invasive method for assessing fat mass, fat-free mass, and percentage body fat in infants.

Participants will be followed monthly up to six months postpartum (or until the infant reaches 6.0 kg, the upper limit for PEAPOD measurement). At each visit, both maternal and infant assessments will be conducted. These include anthropometric measurements, body composition assessments, and collection of biological samples such as maternal venous blood, umbilical cord blood, capillary blood samples, and maternal breast milk. Laboratory analyses will include haematological parameters and nutritional biomarkers relevant to maternal and infant health.

The primary objective is to compare longitudinal changes in body composition between SGA and AGA infants during the first six months of life. Secondary objectives include identifying maternal and fetal factors associated with neonatal and infant body composition, including maternal nutritional status, gestational weight gain, metabolic conditions, and breast milk composition.

This study will provide important evidence on early-life body composition trajectories in a resource-limited setting and may inform strategies to improve maternal and infant health, nutritional interventions, and long-term disease prevention.

Study Type

Observational

Enrollment (Estimated)

300

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Contact

Study Contact Backup

Study Locations

    • Changwat Tak
      • Tak, Changwat Tak, Thailand
        • Mawker Thai Clinic, Shoklo Malaria Research Unit (SMRU)
        • Contact:
        • Principal Investigator:
          • Prof Rose McGready
        • Sub-Investigator:
          • Prof Francois H. Nosten
        • Sub-Investigator:
          • Dr Sue J Lee
        • Sub-Investigator:
          • Dr Nay Win Tun
        • Sub-Investigator:
          • Dr Aung Myat Min
        • Sub-Investigator:
          • Dr Mellie Gilder
        • Sub-Investigator:
          • Dr May Thu Thu Aung
        • Sub-Investigator:
          • Dr Ajjima Thussachan

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

No older than 6 months (Child)

Accepts Healthy Volunteers

N/A

Genders Eligible for Study

All

Sampling Method

Non-Probability Sample

Study Population

Pregnant woman attending for antenatal care or admitted for delivery and their neonates attending at Mawker Thai clinic along the Thailand-Myanmar border. The study population includes both small for gestational age (SGA) and appropriate for gestational age (AGA) neonates and their mothers, representing a resource-limited border population.

Description

Inclusion Criteria:

Pregnant woman

  • The pregnant woman who had received a good dating ultrasound scan less than 24 weeks' gestation and maternal age would be ≥ 18 years old.
  • Willing and able to provide informed consent.
  • Able to attend monthly follow-up visits.

Neonates

  • Normal, single-baby pregnancy (singleton) born at term at Mawker Thai clinic.

    • Neonate eligibility can only be confirmed after delivery.

Exclusion Criteria:

Pregnant woman

  • Families residing far from the study site and unable to commit to follow-up. Neonates*

  • Baby born requiring admission to the special care baby unit (SCBU).

    • Neonate eligibility can only be confirmed after delivery.

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Observational Models: CASE_CONTROL
  • Time Perspectives: PROSPECTIVE

Cohorts and Interventions

Group / Cohort
Intervention / Treatment
Small for Gestational Age (SGA) Neonates

Neonates classified as small for gestational age (SGA), defined as birth weight below the 10th percentile for gestational age. Participants will undergo non-invasive body composition measurements using air-displacement plethysmography (PEAPOD) and follow-up assessments at monthly intervals up to six months of age (or until reaching 6.0 kg). Additional study procedures include anthropometric measurements and collection of biological samples (maternal blood, cord blood, infant capillary blood, and breast milk) for laboratory analyses.

The PEAPOD air displacement plethysmography system is a non-invasive device used to measure infant body composition, including fat mass, fat-free mass, and percentage body fat. The measurement is performed by placing the infant in a calibrated chamber for a short duration, during which body volume and mass are assessed. The procedure is safe, painless, and does not involve radiation or invasive techniques. In this study, the device is used solely for observational measurement of body composition and not as a therapeutic intervention.

Other Names:
  • PEAPOD Infant Body Composition Device
Appropriate for Gestational Age (AGA) Neonates

Neonates classified as appropriate for gestational age (AGA), defined as birth weight between the 10th and 90th percentile for gestational age. Participants will undergo the same study procedures as the SGA group, including non-invasive body composition measurements using PEAPOD and follow-up assessments at monthly intervals up to six months of age (or until reaching 6.0 kg), along with anthropometric measurements and collection of biological samples for laboratory analyses.

The PEAPOD air displacement plethysmography system is a non-invasive device used to measure infant body composition, including fat mass, fat-free mass, and percentage body fat. The measurement is performed by placing the infant in a calibrated chamber for a short duration, during which body volume and mass are assessed. The procedure is safe, painless, and does not involve radiation or invasive techniques. In this study, the device is used solely for observational measurement of body composition and not as a therapeutic intervention.

Other Names:
  • PEAPOD Infant Body Composition Device

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Body composition changes - Fat mass in neonates with small for gestational age (SGA) and appropriate for gestational age (AGA) at birth and during the first 6 months of life
Time Frame: At birth, 1, 2, 3, 4, 5 and 6 months of life (unless body weight >6.0kg is reached first)

Fat mass (kg) measured using air displacement plethysmography (PEAPOD) at birth and during follow-up visits to compare between small for gestational age (SGA) and appropriate for gestational age (AGA) infants

At birth, 1, 2, 3, 4, 5 and 6 months of life (unless body weight >6.0kg is reached first)
Body composition changes - Fat-free mass in neonates with small for gestational age (SGA) and appropriate for gestational age (AGA) at birth and during the first 6 months of life
Time Frame: At birth, 1, 2, 3, 4, 5 and 6 months of life (unless body weight >6.0kg is reached first)

Fat-free mass (kg) measured using PEAPOD at birth and during follow-up visits to compare between SGA and AGA infants

At birth, 1, 2, 3, 4, 5 and 6 months of life (unless body weight >6.0kg is reached first)
Percentage body fat in SGA and AGA infants
Time Frame: At birth, 1, 2, 3, 4, 5 and 6 months of life (unless body weight >6.0kg is reached first)

Percentage body fat (%) measured using PEAPOD at birth and during follow-up visits to compare between SGA and AGA infants

At birth, 1, 2, 3, 4, 5 and 6 months of life (unless body weight >6.0kg is reached first)

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Maternal First-Trimester Body Mass Index (BMI)
Time Frame: Baseline (antenatal records)

Maternal first-trimester BMI (kg/m²) calculated from weight and height recorded during antenatal care

Baseline (antenatal records)
Maternal Gestational Weight Gain
Time Frame: Baseline (antenatal records)

Maternal gestational weight gain (kg) calculated from antenatal weight measurements

Baseline (antenatal records)
Gestational Diabetes Mellitus Status
Time Frame: Baseline (antenatal records)

Presence or absence of gestational diabetes mellitus documented in maternal clinical records

Baseline (antenatal records)
Maternal Anaemia
Time Frame: Baseline to maximum 6 months postpartum

Presence or absence of maternal anaemia determined from maternal haemoglobin measurements

Baseline to maximum 6 months postpartum
Maternal HbA1c Concentration
Time Frame: Delivery and 2 months postpartum

Maternal glycated haemoglobin (HbA1c) percentage (%) measured from maternal blood samples

Delivery and 2 months postpartum
Breast Milk Creamatocrit
Time Frame: At birth to maximum 6 months postpartum

Creamatocrit percentage (%) measured from maternal breast milk samples

At birth to maximum 6 months postpartum
Breast Milk Sodium Concentration
Time Frame: At birth to maximum 6 months postpartum

Sodium concentration (mmol/L) measured from maternal breast milk samples

At birth to maximum 6 months postpartum
Breast Milk Proteomic Profile
Time Frame: Delivery and monthly postpartum until 6 months

Proteomic profile of maternal breast milk measured using MALDI-TOF analysis

Delivery and monthly postpartum until 6 months

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Principal Investigator: Prof Rose McGready, Shoklo Malaria Research Unit

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Estimated)

December 1, 2026

Primary Completion (Estimated)

October 31, 2028

Study Completion (Estimated)

October 31, 2028

Study Registration Dates

First Submitted

April 9, 2026

First Submitted That Met QC Criteria

November 3, 2026

First Posted (Actual)

November 9, 2026

Study Record Updates

Last Update Posted (Actual)

November 9, 2026

Last Update Submitted That Met QC Criteria

November 3, 2026

Last Verified

November 1, 2026

More Information

Terms related to this study

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

IPD Plan Description

Individual participant data (IPD), including de-identified clinical, anthropometric, laboratory, and body composition data collected during the study, will not be made publicly available. Data collected in this study involve sensitive information from mothers and neonates in a vulnerable population, and sharing will be restricted to protect participant confidentiality. De-identified data may be made available upon reasonable request, subject to review and approval by the study investigators and relevant institutional authorities, and in accordance with data sharing agreements and applicable ethical and regulatory requirements.

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

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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