Cortical Activity During Vojta Stimulation in Healthy Adults

Brain Clinical Trial

Official title:

Cortical Activity During Sensorial Tactile Stimulation in Healthy Adults. The Innate Patron Activation With Vojta Therapy.

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT04317950
• Other study ID #: UEMURJC
• Status: Completed
• Phase: N/A
• Start date: January 8, 2020
• Est. completion date: March 15, 2020

Study information

• Verified date: February 2021
• Source: Universidad Rey Juan Carlos
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

The present study is focused on the importance of sensory stimuli at the tactile and proprioceptive level that occur during the activation of the pectoral area, following the treatment protocol of Vojta Therapy (VT), and which are the areas that are activated in the central nervous system (CNS) during stimulation, as well as muscle activity. For the activation record it will be used electroencephalography and electromyography electrods.

Description:

The relationship between intrinsic and extrinsic factors condition the development of the human being. The sensory organs are the main recipients of the information, thanks to them we are able to interact with the environment and register the influence of the stimuli inside the organism. The brain receives information from the environment through its senses.

At the tactile level the brain receives afferent information thanks to the activation of mechanoreceptors of the skin during interaction with the environment. The receivers encode the stimulus information and send it to the specific CNS structures. In these structures, the sensations received are combined and the stimulus is transformed into a perfectly elaborated response, both in a conscious and innate way.

Dr. Vojta showed in 1974 the locomotion reflects the result of the study of motor ontogenesis. This discovery was the demonstration of the existence of innate and preprogrammed motor patterns in Humans.

Most of the studies related to VT have showed the improvements obtained by the patients, validating it as a method of treatment and evidencing objective changes after its application. This research aim to go further and verify that cortical areas are activated during the application of an external and proprioceptive stimuli that are performed during the first phase of VT turning and which areas are responsible for producing and organizing the efferent response.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 40
• Est. completion date: March 15, 2020
• Est. primary completion date: March 1, 2020
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: All
• Age group: 18 Years to 50 Years

Eligibility

Inclusion Criteria:

• Healthy adult population with no history of neurological disease or others that may affect the test.

• Age between 18 and 50 years.

• Not having addiction to alcohol or drugs at the time of the study.

• Not knowing the basics of Vojta Therapy, or knowing the responses of stimuli when applying therapy.

• Not having the pharmacological treatment that affects the functioning of the Central Nervous System and may interfere with the test results.

Exclusion Criteria:

• Those who do not meet the inclusion criteria

• Not having suffered ms-skeletal alterations in the last 6 months.

• Known sensory abnormalities.

• Diagnosis of some neurological pathology or condition that could alter the study such as pain, radiculopathy.

• Refuse to sign the informed consent.

• Claustrophobia.

• Those that can spoil the magnetic resonance image.

• Be a carrier of some metallic material.

• Pregnancy or nursing mother.

• The contraindications of Vojta Therapy.

• Acute diseases that present with fever and / or inflammation.

• Vaccination with live germs, according to medical criteria (usually 10 days after vaccination).

• In case of crystal bone disease, uncontrolled heart disease.

Related Conditions & MeSH terms

• Brain

Intervention

Other:
• Vojta
Reflex locomotion stimulus
• Sham
sham stimulus

Locations

Country	Name	City	State
Spain	Roberto Cano de la Cuerda	Alcorcón	Madrid

Sponsors (2)

Lead Sponsor	Collaborator
Josue Fernandez Carnero	Universidad Europea de Madrid

Country where clinical trial is conducted

Spain, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Electroencephalography (EEG)	EEG power in alpha and beta bands	10 minutes per patient
Primary	Electromyography (EMG)	EMG power in Rectus abdominis, wrist extensors and tibialis anterior	10 minutes per patient