Mobile Health Intervention for Infants in Guatemala (18-m Intervention)

Infant Development Clinical Trial

Official title: Mobile Health Intervention to Promote Positive Infant Health Outcomes in Guatemala

Status Recruiting

Clinical Trial Summary

Promoting optimal development for children at risk in low- and middle-income countries (LMICs) is an important global health priority. Supporting caregivers to provide nurturing care is an evidence-based strategy, however feasibility of scaling-up this supporting is limited by competing demands on health workers' time. For infant development, mHealth technologies have the potential to solve this problem by providing tailored content directly to caregivers, involving and empowering them to promote infant development, promoting and facilitating interactions with health workers when areas of concern are identified and, therefore, expanding the reach of healthcare systems. Following a pilot feasibility study, this current study will examine the effectiveness of a caregiver-directed smartphone application to directly engage first-time caregivers in rural Guatemala and support early childhood development.

Clinical Trial Description

Rationale: According to recent estimates, nore than 40% of children under age 5 residing in low- and middle-income countries (LMICs)-250 million children in total-are at risk of not reaching their developmental potential due to living in environments with malnutrition, poverty, and lack of early stimulation. Mobile health (mHealth) technology represents an efficient strategy for scaling interventions to promote infant development.

Intervention: Individually-randomized controlled trial of mHealth application compared to paper caregiving materials. Length of intervention = 18 months.

Objectives and purpose: We will test the effectiveness of a smartphone application that will directly engage caregivers in providing nurturing care to at-risk infants. We will assess effectiveness of the mHealth application compared to paper caregiving materials by comparing group differences in Bayley scores after 18 months.

Study population: first-time parents of newborn infants, newborn infants. ;

Related Conditions & MeSH terms

• Infant Development

• NCT number: NCT06195358
• Study type: Interventional
• Source: Children's Hospital Los Angeles
• Contact: Beth Smith, PT, DPT, PhD
• Phone: 323-361-4670
• Email: bsmith@chla.usc.edu
• Status: Recruiting
• Phase: N/A
• Start date: January 25, 2024
• Completion date: July 31, 2026