Effect of Transcranial Direct Current Stimulation on Upper Extremity of Children With Hemiparesis
Paraules clau
Resum
Descripció
One in 4000 full-term infants develops arterial ischemic stroke at the time of birth.5 These children are commonly called an infantile stroke, infantile hemiplegia, perinatal stroke, and congenital hemiplegic cerebral palsy. Epileptic seizures are common in 24-45 % of children suffering from an infantile stroke within a month.6 Noninvasive brain stimulation (NIBS) is the novel method of delivering therapeutic currents to the brain for the purpose of diagnosis and treatment 7. There is an exponential increase in researches on the effect of NIBS on cognitive deficits. The NIBS has proven to cause neural modulation at the cortical level8. The effect of stimulation is either increased or decreased in neuronal activity, depending on the anodal and cathodal stimulation, firing rate, and period of the activation or inhibition910. There are two types of NIBS techniques safely practiced among humans, these are, Transcranial Magnetic Stimulation (TMS) and Transcranial Direct Current Stimulation (tCDS)11. tCMS uses a weak magnetic field that transforms into beneficial currents into the brain for diagnostic (Single-pulse tCMS) or treatment purposes (repetitive tCMS). The inhibitory or excitatory cortical effects are achieved by decreasing or increasing the frequency and duration of tCMS 12. tCDS involves the use of weak direct or alternating current applied on the scalp via electrodes for the purpose of neural modulation13. The most popular form of tCDS device is a battery-operated stimulator capable of producing direct current ranging from 0.5-2.0 mA14. Neural modulation is achieved by altering the resting membrane potential. The anode causes increased excitability due to its depolarizing effect whereas the cathode electrode causes inhibition due to the hyperpolarization effect14.
Virtual reality (KVR) is the use of a computer interface involving upper limb activity in pediatric rehabilitation. VR creates an artificial environment, presented to the user through appropriate sensory stimulations. Participants use the motion sensor mounted on the paretic hand to interact with the virtual environment. The participants will receive visual and auditory feedback. The purpose of the study is to evaluate the combined effect of virtual reality activities and tDCS on upper limb activity in children with hemiparesis.
Dates
| Darrera verificació: | 01/31/2020 |
| Primer enviat: | 02/02/2020 |
| Inscripció estimada enviada: | 02/03/2020 |
| Publicat per primera vegada: | 02/05/2020 |
| Última actualització enviada: | 02/04/2020 |
| Publicació de l'última actualització: | 02/06/2020 |
| Data d'inici de l'estudi real: | 01/02/2020 |
| Data estimada de finalització primària: | 03/31/2020 |
| Data estimada de finalització de l’estudi: | 04/30/2020 |
Condició o malaltia
Intervenció / tractament
Device: Experimental group
Other: Control group
Fase
Grups de braços
| Braç | Intervenció / tractament |
|---|---|
| Experimental: Experimental group Transcranial direct stimulation + virtual related group:
Brain stimulator v3.0 will be used to deliver 1.5 mA current over the scalp corresponding to the primary motor cortex. The current will be delivered via two surface electrodes 5 × 5 cm placed on the scalp Virtual reality (KVR) is the use of a computer interface involving upper limb activity in pediatric rehabilitation. VR creates an artificial environment, presented to the user through appropriate sensory stimulations. | Device: Experimental group Brain stimulator v3.0 will be used to deliver 1.5 mA current over the scalp corresponding to the primary motor cortex. The current will be delivered via two surface electrodes 5 × 5 cm placed on the scalp, validated by the previous research |
| Sham Comparator: Control group Sham Transcranial direct stimulation Group + virtual related group; The sham set-up will follow a similar protocol as the experimental group but the intensity of the current will be ceased after 30 seconds of stimulation. Participants in the Sham group will feel the identical sensation as the experimental group and will be unable to differentiate between actual and sham tDCS such procedure is validated in earlier studies. | Other: Control group The sham set-up will follow a similar protocol as the experimental group but the intensity of the current will be ceased after 30 seconds of stimulation. Participants in the Sham group will feel the identical sensation as the experimental group and will be unable to differentiate between actual and sham tDCS such procedure is validated in earlier studies |
Criteris d'elegibilitat
| Edats elegibles per estudiar | 5 Years Per a 5 Years |
| Sexes elegibles per estudiar | All |
| Accepta voluntaris saludables | Sí |
| Criteris | Inclusion Criteria: 1. The congenital stroke survivors with mild to moderate degree of upper limb disability on the Brunnstrom recovery scale16. The scores from 3-4 are considered moderate and 5-6 as a mild degree of upper-limb disability. 2. Age 5-12 years. 3. Able to understand simple commands. 4. Normal vision or with corrected glass Exclusion Criteria: 1. Hemorrhage in the subarachnoid space 2. Aphasia 3. Neurosurgery of brain 4. Seizures in the past 12 months. 5. On medication for seizures. |
Resultat
Mesures de resultats primaris
1. Baseline and post- intervention Fugl-Meyer motor assessment [8 Months]
Mesures de resultats secundaris
1. Beiseline and post- intervention Motricity Index [8 Months]
2. Baseline and post- intervention Modified Barthel Index [8 Months]
