Development, Child

8

Review clinical trials related to Development, Child. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Not yet recruiting

The INICIO-Guatemala Study

The goal of this randomized controlled trial (RCT) is to evaluate an intestinal health-targeted nutritional intervention and a caregiver training program, individually and combined, on childhood neurodevelopment (ND) in rural southwest Guatemala. The main questions it aims to answer are: what is the impact of an intestinal-targeted nutritional intervention on child ND and what is the added benefit of a caregiver intervention on child ND. The primary endpoint is the Mullen Scales of Early Learning (MSEL) Early Learning Composite (ELC) Score at 24 months. Secondary endpoints include MSEL subdomain scores (gross motor, fine motor, expressive language, receptive language, visual reception). Researchers will compare child ND between the four study arms using a factorial design: (1) intestinal health-targeted nutritional intervention, (2) caregiving training program, (3) combined intestinal health-targeted nutritional intervention and caregiving training program, and (4) active control. Participants will be randomized as mother-child dyads at 6 months of age and followed until 24 months of age.

Participants needed: 400
Trial details
Age: 0-50Biological sex: AllType: InterventionalSponsor: University of North Carolina, Chapel HillUpdated: Feb 3, 2026Locations: 1
Eligibility criteria

Pregnant woman in the second trimester of pregnancy [+3]

Pregnant woman less than 15 years of age [+4]

Status: Recruiting

VItamin D in pregnanCy for prevenTion Of eaRlY Childhood Asthma

The overall aim of the study is to develop a nutritional preventive vitamin D supplementation strategy in pregnancy for early childhood asthma/persistent wheeze during the first three years of life as we hypothesize that supplementation in higher doses than recommended could reduce the risk of disease development.

Participants needed: 2,000
Trial details
Phase: Phase 3Age: 18-45Biological sex: FemaleType: InterventionalSponsor: Professor Klaus BønnelykkeUpdated: Sep 30, 2025Locations: 1
Eligibility criteria

Pregnant Danish women before week 26 with blood levels of EPA+DHA above 4.7% of... [+3]

Status: Recruiting

Fish Oil in pREgnancY for Personalized Prevention of Early Childhood Asthma

The overall aim of the study is to develop a nutritional preventive fish oil supplementation strategy in pregnancy for early childhood asthma/persistent wheeze during the first three years of life as we hypothesize that both supplementations in higher doses than recommended could reduce the risk of disease development.

Participants needed: 2,000
Trial details
Phase: Phase 3Age: 18-45Biological sex: FemaleType: InterventionalSponsor: Professor Klaus BønnelykkeUpdated: Sep 30, 2025Locations: 1
Eligibility criteria

Pregnant Danish women before week 26 with blood levels of EPA+DHA below 4.7% of... [+3]

Status: Recruiting

Hands and Hearts Together

Growing evidence demonstrates that secure attachment in childhood predicts children's healthy social, biological, and behavioral functioning, whereas insecure attachment predicts behavior problems and physiological dysregulation; thus, efforts to foster secure attachment are crucial for promoting the healthy development of children and families. This proposal describes a randomized controlled trial (RCT) of an innovative intervention program that can be widely implemented designed to foster children's secure attachment, promote healthy physiological regulation, and reduce the risk for behavior problems: The Circle of Security ® Parenting (COS-P) intervention. To this end, investigators will conduct an RCT with 249 parent-child dyads enrolled or are eligible but not yet enrolled in two diverse Early Head Start (EHS) programs.

Participants needed: 249
Trial details
Age: 8+Biological sex: AllType: InterventionalSponsor: University of Maryland, College ParkUpdated: Jul 3, 2025Locations: 2
Eligibility criteria

Parents whose children (age 8 to 36 months) are enrolled or are eligible to be e...

Parents who are not sufficiently fluent in the language in which COS-P intervent...

Status: Recruiting

Social Transfers for Exclusive Breastfeeding in Brazil

The goal of this study is to assess the effectiveness of social transfers on exclusive breastfeeding rates in São Paulo, Brazil. The main research questions are: 1. Are social transfers effective at increasing exclusive breastfeeding rates 2. Are social transfers effective in prolonging the duration of exclusive breastfeeding 3. Are social transfers effective in prolonging the duration of complementary breastfeeding 4. What are the long-term impacts of social transfers for breastfeeding on child health and development Participants will be randomly assigned to one of three groups: 1) control, no social transfer 2) non-conditional social transfer at 6-months postpartum, and 3) conditional social transfer at six months postpartum; conditional upon the mothers exclusive breastfeeding status. All participants receive education about the benefits of exclusive breastfeeding and current international recommendations. Researchers will compare the intervention groups to the control group to see if social transfers are effective at increasing exclusive breastfeeding rates at six months postpartum.

Participants needed: 400
Trial details
Age: 18-50Biological sex: FemaleType: InterventionalSponsor: Swiss Tropical & Public Health InstituteUpdated: Jun 24, 2025Locations: 2
Eligibility criteria

Gave birth in the last 72 hours [+6]

Plans to move permanently outside study area [+4]

Status: Recruiting

Preventing Vulnerable Child Syndrome in the NICU With Cognitive Behavioral Therapy (PreVNT Trial)

This study is being done to see if outcomes for both a premature infant's parents and the infant born prematurely who have spent time in the neonatal intensive care unit (NICU) can be improved through parent cognitive behavioral therapy (CBT) sessions.

Participants needed: 100
Trial details
Biological sex: AllType: InterventionalSponsor: University of Texas Southwestern Medical CenterUpdated: Jun 13, 2025Locations: 1
Eligibility criteria

Born at Parkland Hospital [+3]

Significant congenital anomalies [+1]

Status: Recruiting

Reference Values for the Muscle Power Sprint Test

The goal of this prospective, cross-sectional study is to develop updated reference values for the Muscle Power Sprint Test (MPST) in children aged 5-12 years. The main question it aims to answer is: • What are reference ('normal') values for the MPST in children aged 5-12 years? Participants will be asked to perform six short sprints of fifteen meters each, with a ten-second rest between each effort.

Participants needed: 480
Trial details
Age: 5-12Biological sex: AllType: InterventionalSponsor: Erasmus Medical CenterUpdated: Feb 25, 2025Locations: 1
Eligibility criteria

Age 5-12 years [+1]

Contra-indication for maximal exercise due to cardiac or respiratory morbidities [+2]

Status: Recruiting

Orchestra in Class, a Novel Booster for Executive Functions and Brain Development in Young Primary School Children

How to optimally stimulate the developing brain is still unclear. Executive functions (EF) exhibited substantially stronger far transfer effects in children who learned to play a musical instrument than in children who acquired other arts. What is crucially lacking is a large-scale, long-term genuine randomized controlled trial (RCT) in cognitive neuroscience, comparing musical instrumental training (MIP) to another art form and a control group. Collected data of this proposal will allow, using machine learning, to build a data-driven multivariate model of children's interconnected brain and EF development over the first 2 years of their academic curriculum (6-8 years), with or without music or other art training.

Participants needed: 150
Trial details
Age: 6-8Biological sex: AllType: InterventionalSponsor: School of Health Sciences GenevaUpdated: Dec 18, 2023Locations: 1
Eligibility criteria

School grade 3P/4P (3rd and 4th year of elementary school (6-8-year-old children... [+4]

Non-consent (children and or parents) [+10]