Acute Effect of tDCS in Young Individuals

Healthy Clinical Trial

Official title:

Acute Effect of tDCS on Motor Performance, Autonomic Control and Attentional and Executive Functions in Young Individuals

Clinical Trial Details — Status: Not yet recruiting

Administrative data

• NCT number: NCT06109727
• Other study ID #: 71695023.3.0000.5347
• Status: Not yet recruiting
• Phase: N/A
• Start date: January 1, 2024
• Est. completion date: December 31, 2024

Study information

• Verified date: October 2023
• Source: Federal University of Rio Grande do Sul
• Contact: Taís Malysz
• Phone: +5551995890622
• Email: tais.malysz[@]ufrgs.br
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

The aim of this study is to investigate the effect of transcranial electrical stimulation (tDCS) on motor performance, autonomic control and attentional and executive functions in young individuals.

Description:

Gait research in young and healthy individuals increases knowledge about the neuromuscular structures involved in this motor act and thus helps to develop or adapt therapeutic approaches that increase performance and/ or optimize the rehabilitation process for people with changes in gait control, and patients with neurological diseases. The aim of this study is to investigate the effect of transcranial electrical stimulation (tDCS) on motor performance, autonomic control and attentional and executive functions in young individuals. A total of 20 individuals (10 women and 10 men) aged 20-30 years will participate in this study. Each participant will visit the laboratory on three occasions, interspersed for one week, one visit for the initial evaluation (approximately 1 hour) and two visits for data collection, lasting approximately 1 hour and 40 minutes each. All participants will be randomly allocated in a double-blind and counterbalanced manner in the different experimental conditions. In one of the visits will be composing the intervention group (n=10; 20 min) and in another visit the Sham group (n=10). Outcomes related to motor performance (bilateral coordination, static and dynamic balance and functional mobility), heart rate variability and attentional and executive functions will be evaluated. To this end, the gait will be analyzed through the OpenCap motion analysis system from filming and after, the phase coordination index will be calculated for analysis of bilateral coordination; the stabilometry test will be used to assess the static balance of the participants, using a force platform where the participant remains standing on the platform to measure the center of pressure; functional mobility will be investigated from the 30-second sit-up test, aiming to analyze the dynamic balance and functional strength of the lower body, and the Timed up and Go Test used for balance analysis, gait and functional capacity. Heart rate variability will be recorded from the use of the Polar Vantage heart rate monitor (Finland), with the capacity of the R-R temporal record. The attentional and executive functions will be evaluated from the Stroop Test tool. These are three tasks with 24 items each, where the participant will be evaluated according to how quickly he performs the task and the amount of errors presented. The data will be described as mean. The normality of all data will be verified by the Shapiro-Wilk test. ANOVA with repeated measures of two factors will be used, followed by the Bonferroni post hoc test to compare the variables collected between the different conditions of brain stimulation (with and without application of tDCS) and between gait conditions. One-factor ANOVA will be used for brain stimulation conditions; data will be tabulated via Excel and statistical analyses will be performed in the SPSS software package for Windows version 24.0 (IBM, Chicago, USA). A significant value of p < 0.05 will be considered.

Recruitment information / eligibility

• Status: Not yet recruiting
• Enrollment: 20
• Est. completion date: December 31, 2024
• Est. primary completion date: June 30, 2024
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: All
• Age group: 20 Years to 30 Years

Eligibility

Inclusion Criteria:

• 20-30 years
• participant of both sex

Exclusion criteria:

• history of neurological or psychological diseases;
• use of any medications that may affect balance control, such as sedative drugs;
• presence of skeletal muscle injuries such as fracture, ligament injury, muscle tension or low back pain that restricts movement;
• presence of any sign of involvement of the spinal cord;
• visual or hearing impairment;
• musculoskeletal deformities in the lower or upper extremities that may affect the participant's standing posture;
• skin conditions (e.g., eczema and injuries) on the scalp
• presence of metal inside the head (outside the mouth) such as splinters, surgical clips or fragments of solder or metal work;
• implanted devices such as cardiac pacemaker, cochlear implant;
• score less than 24 points in the Mini Mental State Examination (MMSE)

Related Conditions & MeSH terms

• Healthy

Intervention

Device:
• cerebellar transcranial electrical stimulation
Cerebellar transcranial electrical stimulation - 20 mA - 20 min

Locations

Country	Name	City	State
Brazil	Tais Malysz	Porto Alegre	RS

Sponsors (1)

Lead Sponsor	Collaborator
Federal University of Rio Grande do Sul

Country where clinical trial is conducted

Brazil, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Effect of tDCS on motor performance	Bilateral coordination of different walking conditions will be assessed by percentage (%); The static equilibrium will be evaluated by the average amplitude of displacement of the center of pressure in mean lateral and anteroposterior directions (cm)	Through study completion, an average of 1 year
Secondary	Effect of tDCS on functional mobility and dynamic balance	The 30-second sit and stand test - data expressed in number of repetitions The Time Up and Go Test (TUG) - data expressed in time(s)	Through study completion, an average of 1 year
Secondary	Effect of variability of the heart rate	heart rate per min	Through study completion, an average of 1 year
Secondary	Efect of tDCS on attentional and executive functions	time (s) to realize cognitives testes (Stroob test)	Through study completion, an average of 1 year