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NOT YET RECRUITING

NCT07784231

PHASE1/PHASE2

The Use of Photobiomodulation in the Treatment of Spasticity After Stroke.

Sponsor: University of Nove de Julho

View on ClinicalTrials.gov

Summary

Stroke is a non-progressive and permanent syndrome in adults, with approximately 60% of patients presenting with spastic hemiparesis. Spasticity leads to changes in the physiological pattern of muscle tissue contraction and hemodynamics, and, when left untreated, negatively impacts functionality. Photobiomodulation (PBM) has demonstrated positive effects on tissue regeneration, muscle relaxation, reduction of inflammation, fatigue, and pain relief in various muscular and neurological disorders. Methods: This blinded, randomized, controlled clinical trial aims to evaluate the effects of PBM on triceps surae muscle spasticity in adults with stroke. Forty-two participants with spastic hemiparesis post-stroke will be randomized into two groups: active PBM (850 nm, 200 mW, 4 J/point in the gastrocnemius, 12 points, weekly for 8 weeks) or placebo PBM (same protocol, device switched off). Both groups will receive the institute's standard rehabilitation treatment. Outcomes will be assessed using the Modified Ashworth Scale (MAS), ankle range of motion, presence of pain, amount of antispastic medication in use, contraction strength (by manual examination) muscle oxygenation (by transcutaneous near-infrared spectroscopy), functionality, and the occurrence of adverse events before and after the intervention. At the end of recruitment, comparisons between groups and between time points will be performed and statistically analyzed using a two-way repeated means ANOVA test and the Generalized Estimating Equations (GEE) test. We also foresee a pilot interim analysis when recruitment reaches a size of 10 participants per group. This interim analysis will be performed using a two-way/means ANOVA to assess effect size and recalculate sample size, making adjustments to the design if necessary.

Official title: The Use of Photobiomodulation in the Treatment of Spasticity After Stroke: a Blinded Clinical Trial.

Key Details

Gender

All

Age Range

18 Years - Any

Study Type

INTERVENTIONAL

Enrollment

Start Date

2026-08

Completion Date

2027-06-30

Last Updated

2026-08-25

Healthy Volunteers

Conditions

Stroke Spasticity Photobiomodulation NIRS

Interventions

RADIATION

Photobiomodulation Therapy

Photobiomodulation (PBM)-formerly referred to as low-level laser therapy (LLLT) or cold laser therapy-is a non-invasive, non-thermal therapeutic modality that employs light in the red to near-infrared spectrum (typically spanning wavelengths from approximately 600 nm to 1,100 nm) to elicit beneficial biological responses in target tissues. The underlying mechanism of action is primarily photochemical rather than photothermal: photons delivered to the tissue are absorbed by endogenous chromophores, most notably cytochrome \*c\* oxidase (CCO), a key enzyme in the mitochondrial electron transport chain. This absorption transiently increases mitochondrial membrane potential, augments adenosine triphosphate (ATP) synthesis, and modulates the generation of reactive oxygen species (ROS). These primary mitochondrial events subsequently trigger a cascade of secondary intracellular signaling pathways-including the activation of transcription factors such as nuclear factor kappa-B (NF-κB) and hypox

RADIATION

Placebo PBM

Application of transcutaneous PBM therapy - device switched off- to the gastrocnemius muscles

OTHER

Standard Multidisciplinary Rehabilitation Program for Spasticity

A comprehensive, multidisciplinary intervention delivered by a specialized team-including physical therapists and rehabilitation physicians-who collaboratively develop an individualized treatment plan tailored to each patient's functional deficits, baseline mobility, and specific spasticity profile. The physical therapy component emphasizes a combination of passive and active stretching protocols, therapeutic exercise to strengthen agonist muscles and improve motor control, gait and balance training, and adjunctive modalities such as neuromuscular electrical stimulation or therapeutic ultrasound, all administered at a frequency and intensity commensurate with the patient's tolerance and clinical progression. Concurrently, the multidisciplinary team addresses associated impairments through therapy focused on activities of daily living and limb function, pharmacological management with oral or antispastics injections as indicated

Inclusion Criteria: * Adults who have sustained a unilateral ischemic or hemorrhagic cortical motor stroke, with the diagnosis documented in the acute phase by computed tomography (CT) or magnetic resonance imaging (MRI); * Patients currently undergoing multidisciplinary rehabilitation at the Rehabilitation Center where the study will be conducted; * Patients presenting with a motor pattern of spastic hemiparesis secondary to stroke; * Patients demonstrating the ability to perform orthostatism (standing posture) or therapeutic or functional gait activity. Exclusion Criteria: * Presence of uncontrolled systemic diseases, including but not limited to cancer, active infections, or uncontrolled diabetes mellitus; * History of photosensitivity or known hypersensitivity to light exposure; * Triceps surae spasticity graded as 4 on the Modified Ashworth Scale (MAS) at the initial pre-screening assessment;Acute clinical instability or any acute medical condition requiring immediate intervention; * Fixed anatomical deformities of the ankle joint that preclude a minimum passive or active range of motion of at least 60 degrees; * Malnutrition or significant nutritional deficiencies;Acute clinical conditions with the potential to exacerbate spasticity, such as acute fractures, cutaneous ulcers, or acute infections;Presence of any other movement or tone disorder (e.g., dystonia, chorea, or parkinsonism) that could confound spasticity assessments; * Exposed tumors or undiagnosed lesions in the area to be irradiated; * Change in the pharmacological class of antispastic medications during the therapeutic period of the study. Dose adjustments within the same medication class will be permitted and documented; * Administration of botulinum toxin type A injections into the triceps surae muscle during the study period or within six months prior to study enrollment; * Discontinuation of the concomitant physical therapy rehabilitation program, even if the participant continues to receive photobiomodulation per the study protocol; * Occurrence of any adverse event attributable to photobiomodulation; * Death; * Withdrawal of informed consent.