Innovations in assistive technology in pediatric Duchenne muscular dystrophy: A scoping review

Pooja Mehra1, Sunita Sharma1

  • 1Maharishi Markandeshwar Institute of Physiotherapy and Rehabilitation, Maharishi Markandeshwar (Deemed to be University), Mullana, Ambala, Haryana, India.

Brain & Development
|May 26, 2026
PubMed

Insights

Assistive technologies show promise for improving the quality of life and function in children with Duchenne muscular dystrophy (DMD). Further research with robust clinical trials is needed to confirm efficacy and integrate these innovations into standard care.

Area of Science:

  • Biomedical Engineering
  • Rehabilitation Technology
  • Pediatric Neuromuscular Disorders

Background:

  • Duchenne muscular dystrophy (DMD) is a progressive X-linked genetic disorder causing muscle weakness and loss of mobility.
  • Increased survival rates in DMD necessitate advanced assistive technologies for daily living and improved quality of life.
  • There is a growing need to understand current assistive technology advancements for children with DMD.

Purpose of the Study:

  • To systematically review recent assistive technologies for children with DMD.
  • To identify emerging research trends and existing gaps in assistive technology literature for DMD.
  • To inform future development and clinical application of these technologies.

Main Methods:

  • Systematic literature search of PubMed, PEDro, and Scopus databases up to November 2025.
  • Adherence to the PRISMA ScR protocol for study selection and data synthesis.
  • Narrative synthesis of data focusing on device types, functional domains, outcomes, and limitations.

Main Results:

  • Twenty studies were included, featuring exoskeletons, robotic devices, virtual reality, wearable sensors, and orthotics.
  • Technologies explored include gait exoskeletons, robotic assistance, virtual reality interventions, and wearable sensor systems.
  • Identified limitations include small sample sizes, short follow-up periods, prototype designs, and inconsistent outcome measures.

Conclusions:

  • Assistive technologies hold potential to enhance quality of life and functional abilities in children with DMD.
  • Well-designed clinical trials with long-term follow-up are crucial for establishing clinical efficacy and feasibility.
  • User-centered design and integration into standard pediatric rehabilitation are key for successful implementation.
Abstract