# Impact of a mobile health intervention on health management among children with phenylketonuria based on a multi-theory model of the behavior change wheel theory and family health theory: protocol for a randomized controlled trial

**Authors:** Jie Wang, Sihan Yang, Jing Wang, Bo Zhu, Yan Wang, Lirong Zhao, Wenli Wang, Ge Li, Fei Wang, Xiaohua Wang

PMC · DOI: 10.3389/fpsyt.2025.1583804 · Frontiers in Psychiatry · 2025-05-27

## TL;DR

This study tests a mobile health app to help manage phenylketonuria in children by improving diet and family involvement.

## Contribution

The study introduces a novel mHealth intervention model based on behavior change and family health theories for PKU management.

## Key findings

- The mHealth intervention is expected to improve dietary adherence and health knowledge in PKU families.
- The model may enhance clinical outcomes and quality of life for children with PKU.
- The approach could be scalable to other regions for broader health management solutions.

## Abstract

Phenylketonuria (PKU) is a hereditary metabolic disorder caused by mutations in the phenylalanine hydroxylase (PAH) gene, leading to the accumulation of phenylalanine (Phe) in the blood. Without timely treatment, PKU patients may develop irreversible intellectual and neurocognitive deficits. The primary treatment for PKU is a strict low-Phe diet, which must be initiated in early life to achieve better outcomes. Therefore, parents and parents’ caregivers play a crucial role in dietary management. However, poor dietary adherence and inadequate health knowledge significantly affect treatment efficacy. Mobile health (mHealth) interventions, as an emerging health management approach, offer personalized, low-cost, and highly accessible solutions. This study aims to develop and evaluate an mHealth intervention model based on the Behavior Change Wheel (BCW) theory and family health theory to improve health management for children with PKU.

This single-center, single-blind randomized controlled trial will be conducted at the Inner Mongolia Maternity and Child Health Care Hospital in China from March to September 2025. Participants will include children with PKU and their parents’ caregivers, who will be randomly assigned to either the intervention group (receiving mHealth interventions via WeChat) or the control group (receiving routine health education). The intervention will include health education, dietary management, regular monitoring reminders, and online consultation services. The primary outcome will be the serum phenylalanine and tyrosine levels of the children. Secondary outcomes will include nutritional indicators, intellectual development indicators, and the caregivers’ health knowledge, compliance, and mental health. Data collection will occur at baseline and at 3 and 6 months post-intervention.

By integrating the BCW and family health theories, this study innovatively develops an mHealth-based health management intervention model for PKU. This model is expected to enhance family health management capabilities and improve clinical outcomes and quality of life for children with PKU. If effective, this model can be extended to other regions to provide more convenient and efficient health management solutions for PKU patients.

## Linked entities

- **Genes:** PAH (phenylalanine hydroxylase) [NCBI Gene 5053]
- **Chemicals:** phenylalanine (PubChem CID 994), tyrosine (PubChem CID 1153)
- **Diseases:** phenylketonuria (MONDO:0009861), PKU (MONDO:0009861)

## Full-text entities

- **Genes:** PAH (phenylalanine hydroxylase) [NCBI Gene 5053] {aka PH, PKU, PKU1}
- **Diseases:** intellectual and neurocognitive deficits (MESH:C537761), PKU (MESH:D010661), hereditary metabolic disorder (MESH:D009386)
- **Chemicals:** tyrosine (MESH:D014443), Phe (MESH:D010649)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

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## References

52 references — full list in the complete paper: https://tomesphere.com/paper/PMC12150297/full.md

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Source: https://tomesphere.com/paper/PMC12150297