Transcranial Photobiomodulation for Spasticity in Pediatric Cerebral Palsy: A Scoping Review of Neurodevelopmental

Amalio Jiménez1, Frederick R Carrick1,2,3,4,5, Monèm Jemni1,2,6

  • 1The Carrick Institute, Cape Canaveral, FL 32920, USA.

Brain Sciences
|March 27, 2026
PubMed

Insights

Evidence for transcranial photobiomodulation (tPBM) in pediatric cerebral palsy (CP) spasticity is severely limited. Current studies lack rigor and standardization, indicating tPBM is an unproven experimental intervention for children with CP.

Area of Science:

  • Neurology
  • Pediatric Rehabilitation
  • Biomedical Engineering

Background:

  • Spasticity affects over 80% of children with cerebral palsy (CP), significantly impacting their disability.
  • Transcranial photobiomodulation (tPBM) is an emerging non-invasive neuromodulatory technique.
  • Existing evidence on tPBM for pediatric CP spasticity is fragmented and insufficient.

Purpose of the Study:

  • To systematically map the existing literature on tPBM for spasticity in pediatric CP.
  • To characterize neurodevelopmental considerations, treatment protocols, functional outcomes, and methodological gaps.
  • To assess the current state of evidence for tPBM in this population.

Main Methods:

  • Scoping review following PRISMA-ScR guidelines.
  • Systematic search of eight databases (January 2000 - September 2025).
  • Inclusion criteria: children (0-18 years) with CP and spasticity, investigating transcranial PBM.

Main Results:

  • Only five primary studies (n=45 children) met inclusion criteria; only two used tPBM.
  • Severe heterogeneity and lack of protocol standardization, including inconsistent or implausible dosimetry.
  • Methodological quality is pre-preliminary; no sham-controlled or blinded trials exist.
  • Reported spasticity reductions and motor improvements are unreliable due to high risk of bias.

Conclusions:

  • Evidence for tPBM in pediatric CP spasticity is in a pre-preliminary stage.
  • Critical limitations include a small study number, lack of methodological rigor, and absence of pediatric safety protocols.
  • Foundational, sham-controlled, double-blind trials with standardized dosimetry are urgently needed.

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