Sensory-motor and cardiorespiratory sensory rehabilitation associated with transcranial photobiomodulation in patients with central nervous system injury: Trial protocol for a single-center, randomized, double-blind, and controlled clinical trial

Ana Paula Pinto, Carolina Lobo Guimarães, Gabriela Aparecida da Silveira Souza, Patrícia Sardinha Leonardo, Marcele Florêncio das Neves, Fernanda Pupio Silva Lima, Mário Oliveira Lima, Rodrigo Alvaro Brandão Lopes-Martins, Ana Paula Pinto, Carolina Lobo Guimarães, Gabriela Aparecida da Silveira Souza, Patrícia Sardinha Leonardo, Marcele Florêncio das Neves, Fernanda Pupio Silva Lima, Mário Oliveira Lima, Rodrigo Alvaro Brandão Lopes-Martins

Abstract

Background: Central nervous system diseases such as stroke, spinal cord injury, traumatic brain injury, and multiple sclerosis can be fatal or cause sequelae, affecting sensorimotor and cardiorespiratory systems and quality of life. These subjects present a low response to aerobic and resistance exercise, due to decreased recruitment of muscle fibers and reduction of metabolic capacity. Aerobic exercises bring benefits in terms of fatigue retardation, gait improvement, regulation of the autonomic nervous system, neuroprotection of the brain, stimulation of the production of endogenous neutrotransmitters related to general well-being, and a favoring of neuroplasticity. Photobiomodulation (PBM Therapy) (previously known as low-level laser therapy), and especially transcranial PBM Therapy, has shown benefits in animals and humans such as cognitive improvement, memory, and behavioral improvement, including attenuation of depression and anxiety, and increased cortical oxygenation. The aims of this trial will be to evaluate the parameters related to the function of the musculoskeletal and cardiorespiratory system and the impact of PBM therapy on these parameters, as part of a rehabilitation and training program for people with reduced mobility.

Methods: This is a randomized, double-blind, placebo-controlled trial with 3 groups: Control, only cardiorespiratory rehabilitation (CCR), CCR with PBM Therapy (CR-PBM), CCR and placebo PBM Therapy (CR-PlaceboPBM). n = 90, 30 per group. PBM Therapy parameters: 810 nm laser, 0.028 cm, 100 mW, 3.5 W/cm, 30 seconds per point, 3 J per point, 107.1 J /cm to 3 electroencephalogram points F7 and F8 and AFz. The trial will be conducted at the University Clinics and the sessions will be 1 hour twice a week for 9 weeks. Baseline, intermediate (4th week), final (9th week), and 2-month follow-up will be performed. Muscular activation, heart rate variability, lung volumes and capacities, fatigability, exercise tolerance, cognition, and quality of life at baseline will be evaluated. Subsequent to baseline evaluations, the PBM Therapy groups will be offered laser therapy (active or inactive); all groups will then receive CCR.

Trial registration number: ClinicalTrials.gov ID - NCT03751306 (approval date: November 22, 2018).

Conflict of interest statement

The authors declare no conflicts of interest.

Figures

Figure 1
Figure 1
Flow diagram of trial.
Figure 2
Figure 2
Rehabilitation station and physical activity BrainMov.

References

    1. GBD 2015 Neurological Disorders Collaborator Group. Global, regional, and national burden of neurological disorders during 1990–2015: a systematic analysis for the Global Burden of Disease Study 2015. Lancet Neurol 2017;16:877–97.
    1. Shams T, Auchus AP, Oparil S, et al. Baseline quality of life and risk of stroke in the ALLHAT Study (Antihypertensive and Lipid-Lowering Treatment to Prevent Heart Attack Trial). Stroke 2017;48:3078–85.
    1. Biering-Sørensen F, Noonan VK. Standardization of data for clinical use and research in spinal cord injury. Brain Sci 2016;6:pii: E29.
    1. Reis C, Wang Y, Akyol O, et al. What's new in traumatic brain injury: update on tracking, monitoring and treatment. Int J Mol Sci 2015;16:11903–65.
    1. Moss BP, Rensel MR, Hersh CM. Wellness and the role of comorbidities in multiple sclerosis. Neurotherapeutics 2017;14:999–1017.
    1. Zorowitz RD, Wein TH, Dunning K, et al. A screening tool to identify spasticity in need of treatment. Am J Phys Med Rehabil 2017;96:315–20.
    1. Graham LA. Management of spasticity revisited. Age Ageing 2013;42:435–41.
    1. Nalysnyk L, Papapetropoulos S, Rotella P, et al. OnabotulinumtoxinA muscle injection patterns in adult spasticity: a systematic literature review. BMC Neurol 2013;13:118.
    1. das Neves MF, Dos Reis MC, de Andrade EA, et al. Effects of low-level laser therapy (LLLT 808 nm) on lower limb spastic muscle activity in chronic stroke patients. Laser Med Sci 2016;31:1293–300.
    1. Dhindsa MS, Merring CA, Brandt LE, et al. Muscle spasticity associated with reduced whole-leg perfusion in persons with spinal cord injury. J Spinal Cord Med 2011;34:594–9.
    1. West CR, Campbell IG, Shave RE, et al. Resting cardiopulmonary function in Paralympic athletes with cervical spinal cord injury. Med Sci Sports Exerc 2012;44:323–9.
    1. Block VA, Pitsch E, Tahir P, et al. Remote physical activity monitoring in neurological disease: a systematic review. PLoS One 2016;11:e0154335.
    1. Hassett LM, Moseley AM, Tate R, et al. Fitness training for cardiorespiratory conditioning after traumatic brain injury. Cochrane Database Syst Rev 2008;16:CD006123.
    1. Morawietz C, Moffat F. Effects of locomotor training after incomplete spinal cord injury: a systematic review. Arch Phys Med Rehabil 2013;94:2297–308.
    1. Baert I, Daly D, Dejaeger E, et al. Evolution of cardiorespiratory fitness after stroke: a 1-year follow-up study. Influence of prestroke patients’ characteristics and stroke-related factors. Arch Phys Med Rehabil 2012;93:669–76.
    1. Coote S, Uszynski M, Herring MP, et al. Effect of exercising at minimum recommendations of the multiple sclerosis exercise guideline combined with structured education or attention control education: secondary results of the step it up randomised controlled trial. BMC Neurol 2017;17:119.
    1. Schiffer F, Johnston AL, Ravichandran C, et al. Psychological benefits 2 and 4 weeks after a single treatment with near infrared light to the forehead: a pilot study of 10 patients with major depression and anxiety. Behav Brain Funct 2009;5:46.
    1. Xuan W, Vatansever F, Huang L, et al. Transcranial low-level laser therapy enhances learning, memory, and neuroprogenitor cells after traumatic brain injury in mice. J Biomed Opt 2014;19:108003.
    1. Wu Q, Xuan W, Ando T, et al. Low-level laser therapy for closed-head traumatic brain injury in mice: effect of different wavelengths. Lasers Surg Med 2012;44:218–26.
    1. Henderson TA, Morries LD. Near-infrared photonic energy penetration: can infrared phototherapy effectively reach the human brain? Neuropsychiatr Dis Treat 2015;11:2191–208.
    1. Beltrame T, Ferraresi C, Parizotto NA, et al. Light-emitting diode therapy (photobiomodulation) effects on oxygen uptake and cardiac output dynamics during moderate exercise transitions: a randomized, crossover, double-blind, and placebo-controlled study. Lasers Med Sci 2018;33:1065–71.
    1. Thunshelle C, Hamblin MR. Transcranial low-level laser (light) therapy for brain injury. Photomed Laser Surg 2016;34(12.):
    1. Hennessy M, Hamblin MR. Photobiomodulation and the brain: a new paradigm. J Opt 2017;19:013003.
    1. Tian F, Hase SN, Gonzalez-Lima F, et al. Transcranial laser stimulation improves human cerebral oxygenation. Lasers Surg Med 2016;48:343–9.
    1. BRAINMOV. Equipment. Available at: Accessed April 13, 2018.
    1. Herdy AH, López-Jiménez F, Terzic CP, et al. South American guidelines for cardiovascular disease prevention and rehabilitation. Arq Bras Cardiol 2014;103suppl 1:1–31.
    1. Batty GD. Physical activity and coronary heart disease in older adults. A systematic review of epidemiological studies. Eur J Public Health 2002;12:171–6.
    1. Lee YK, Kim BR, Han EY. Peak cardiorespiratory responses of patients with subacute stroke during land and aquatic treadmill exercise. Am J Phys Med Rehabil 2017;96:289–93.
    1. Popok DW, West CR, McCracken L, Krassioukov AV. Effects of early and delayed initiation of exercise training on cardiac and haemodynamic function after spinal cord injury. Exp Physiol 2017;102:154–63.
    1. Saunders DH, Sanderson M, Hayes S, et al. Physical fitness training for stroke patients. Cochrane Database Syst Rev 2016;CD003316.
    1. Van der Scheer JW, Martin Ginis KA, Ditor DS, et al. Effects of exercise on fitness and health of adults with spinal cord injury. Neurology 2017;89:736–45.
    1. Chin LM, Chan L, Woolstenhulme JG, et al. Improved cardiorespiratory fitness with aerobic exercise training in individuals with traumatic brain injury. J Head Trauma Rehabil 2015;30:382–90.
    1. Zaizar ED, González-Lima F, Telch MJ. Singular and combined effects of transcranial infrared laser stimulation and exposure therapy: a randomized clinical trial. Contemp Clin Trials 2018;72:95–102.
    1. Blanco NJ, Saucedo CL, Gonzalez-Lima F. Transcranial infrared laser stimulation improves rule-based, but not information-integration, category learning in humans. Neurobiol Learn Memory 2017;139:69–75.

Source: PubMed

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