CClinicalTrials.gg
RecruitingNCT07784231DarbarIlloraUpdated Sep 1, 2026

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

A Phase 1/2 interventional study of Photobiomodulation Therapy and Placebo PBM in Stroke, Spasticity and Photobiomodulation, sponsored by University of Nove de Julho. Recruiting at 1 site in Brazil. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2026-09-01.

Sponsored by University of Nove de Julho · Phase 1/2, Interventional, and Treatment

Phase
Phase 1/2
Study type
Interventional
Enrollment
42
Allocation
Randomized
Ages
18 Years and older
Sex
All
01

Study 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.

Read the detailed description

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.

02

Conditions studied

  • Stroke
  • Spasticity
  • Photobiomodulation
  • NIRS

Keywords

  • stroke
  • photobiomodulation
  • spasticity
  • NIRS
03

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No

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

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.
04

Study design

Phase
Phase 1 / Phase 2
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Triple (Participant, Care provider, Investigator)
Enrollment
42 participants (estimated)

Study arms

  • Experimental
    PBM group

    Application of transcutaneous PBM therapy to the gastrocnemius muscles of the hemiparetic limb associated with standardized rehabilitation therapies according to the institution's protocol

    Radiation: Photobiomodulation Therapy · Other: Standard Multidisciplinary Rehabilitation Program for Spasticity

  • Placebo comparator
    Placebo

    Application of transcutaneous PBM therapy - device switched off- to the gastrocnemius muscles of the hemiparetic limb associated with standardized rehabilitation therapies according to the institution's protocol

    Radiation: Placebo PBM · Other: Standard Multidisciplinary Rehabilitation Program for Spasticity

Interventions

  • RadiationPhotobiomodulation 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

    Also known as: Low level Laser Therapy

  • RadiationPlacebo PBM

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

  • OtherStandard 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

05

What researchers measure

Primary outcomes

  1. Spasticity Grade

    The change in triceps surae spasticity severity, assessed using the Modified Ashworth Scale (MAS). The MAS is a widely validated, clinician-rated ordinal scale that quantifies muscle hypertonia by measuring the resistance encountered during passive joint mobilization; it grades spasticity from 0 (no increase in muscle tone) through 4 (affected part rigid in flexion or extension), with intermediate scores of 1, 1+, 2, and 3 denoting progressively greater degrees of resistance and catch phenomena throughout the range of motion.

    Time frame: Baseline" or "Day 1" and * through study completion, an average of 8 weeks. It will also be assessed immediately before and after each PBM session.

  2. Spasticity Grade

    Quantity of antispastic medications used. Information regarding the medications (class, quantity, dose, and route of administration) used by participants for the treatment of spasticity before and after the end of the 8-week therapeutic period will be collected from medical records.

    Time frame: Baseline" or "Day 1" and * through study completion, an average of 8 weeks.

Secondary outcomes

  1. Pain Intensity

    The presence of pain in the cutaneous reference region of the triceps surae will be assessed using a Numerical Pain Scale (NPS) / The NPS is an aid in measuring the intensity of pain felt by the patient, an important instrument to verify progress and analyze the treatment instituted. The participant should be asked about their level of pain, where 0 means total absence of pain and 10 the maximum pain level.

    Time frame: Baseline" or "Day 1" , and immediately before and after each weekly PBM session and through study completion, an average of 8 weeks

  2. Active and Passive Ankle Range of Motion

    Active and passive range of motion (ROM) of the ankle joint on the affected hemibody will be assessed using standard goniometry. Goniometric measurement is a reliable and widely accepted clinical method for quantifying joint mobility, performed with a universal goniometer aligned to the anatomical landmarks of the ankle joint complex. Active ROM will be measured with the participant performing the ankle movement independently through the available range, whereas passive ROM will be measured with the examiner passively mobilizing the joint through its full available range of motion, ensuring that no excessive force is applied (McRae, 2011). This outcome provides an objective indicator of joint mobility impairment and allows for the evaluation of treatment-related changes in musculoskeletal restriction secondary to spasticity.

    Time frame: Baseline" or "Day 1" and * through study completion, an average of 8 weeks

  3. Functional Independence

    Functional status will be assessed using the Functional Independence Measure (FIM) is an 18-item, 7-point ordinal scale that evaluates the level of assistance required for activities of daily living across motor and cognitive domains, with higher scores indicating greater independence .

    Time frame: Baseline" or "Day 1" and * through study completion, an average of 8 weeks

  4. Motor recovery

    the lower-extremity motor subscale of the Fugl-Meyer Assessment (FMA-LE) will be employed to evaluate sensorimotor recovery, focusing on volitional movement, coordination, and reflex activity of the affected lower limb; this scale is scored on a 3-point ordinal system (0 = no performance, 1 = partial performance, 2 = full performance), with higher scores reflecting better motor function (Shim, 2025).

    Time frame: Baseline" or "Day 1" and * through study completion, an average of 8 weeks

  5. Oxygenation of the Gastrocnemius Muscles

    To assess the oxygenation of the gastrocnemius muscles in real time, a non-invasive transcutaneous muscle oxygen sensor using near-infrared spectroscopy will be employed

    Time frame: Baseline" or "Day 1" , on fifth PBM session, and * through study completion, an average of 8 weeks

  6. Contraction force of the triceps surae

    Triceps surae muscle strength manual test (Polkey, 1977) MRC

    Time frame: Baseline" or "Day 1" and * through study completion, an average of 8 weeks

Other outcomes

  1. Adverse effects

    Any adverse effect related to PBM founded after study will be report

    Time frame: Baseline" or "Day 1" and weekly after each PBM session and through study completion, an average of 8 weeks

  2. Epidemiological Data

    Epidemiological data will be collected from medical records: Age, Gender, Etiology of stroke, medications used, motor dominance, injury time, stroke type, lesion location, affected side, comorbidities, and use of orthoses will be collected from medical records.

    Time frame: Baseline" or "Day 1" and weekly after each PBM session and through study completion, an average of 8 weeks

06

Study locations

1 of 1 sites recruiting
  • CER II Guarulhos
    São Paulo, São Paulo 05020-000, Brazil
    Recruiting
07

References and documents

Individual participant data

Plan to share: Undecided

No publications or documents are linked to this record.

08

Registry details

Key details

Study ID
NCT07784231
Lead sponsor
University of Nove de Julho
Responsible party
Rebeca Boltes Cecatto (Professor M.D. Ph.D. Rebeca Boltes Cecatto, University of Nove de Julho) — Principal investigator
First posted
Aug 25, 2026
Start date
Aug 28, 2026
Primary completion
Apr 30, 2027 (estimated)
Completion
Jun 30, 2027 (estimated)
Last update
Sep 1, 2026

Study contacts

Rebeca B Cecatto, MD, Ph.D.
Contact
rebeca.boltes@gmail.com
+55 11970842496

Oversight

Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
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