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NCT05170906 Clinical Trial

Cerebral Oxygenation During Vojta Therapy in Healthy Adults Using Near-infrared Spectroscopy

Healthy Clinical Trial

Official title:
Cerebral Oxygenation During Vojta Therapy in Healthy Adults Using Near-infrared Spectroscopy

Clinical Trial Details — Status: Not yet recruiting

Administrative data
NCT number NCT05170906
Other study ID # VojaNeurousal
Secondary ID
Status Not yet recruiting
Phase N/A
First received
Last updated
Start date April 1, 2022
Est. completion date December 1, 2022

Study information
Verified date December 2021
Source University of Salamanca
Contact Juan Luis S Sánchez González, PhD
Phone 660738949
Email juanluissanchez@usal.es
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

A randomized clinical trial on a cohort of healthy subjects of legal age, both sexes, recruited from the university community and who will be randomly distributed into two groups (experimental and control). The objective is to assess neurophysiological activation by measuring oxygenation in the supplementary motor and premotor areas of oxygenation in the supplementary motor and premotor areas, through near infrared spectroscopy (NIRS) in healthy subjects spectroscopy (NIRS) in healthy subjects during the application of Vojta Therapy.

Recruitment information / eligibility
Status Not yet recruiting
Enrollment 16
Est. completion date December 1, 2022
Est. primary completion date September 1, 2022
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 40 Years
Eligibility Inclusion Criteria: - Over 18 years old. - Under 40 years old. - Full cognitive capacity. Exclusion Criteria: - Subjects with neuro-muscular pathologies that affect the abdominal muscles, previous surgeries in the area or any chronic neurological or organic disorder that may alter the results. - Vaccinated in the 10 days prior to the intervention - Fever

Study Design

Related Conditions & MeSH terms

Intervention

Other:
• Reflex locomotion stimulus
The therapy consists of the application of a stimulating pressure in the pectoral area in the pattern of the locomotion complex of reflex rolling in its first phase. For this, the subject will be placed in a supine position aligned with respect to the axial axis, with the arms along the body, the lower extremities in extension, and the head extended with a rotation of approximately 30º towards one side of the stimulation. The manual stimulation pressure will be exerted in the space between the 6th-7th or the 7th-8th rib under the mammillary line, with a force of about 2 kg.
• sham stimulus
The control group will receive an application in an area with low receptor density located on the thigh, with a force of about 2 kg.

Locations
Country Name City State
Spain Juan Luis Sánchez González Salamanca

Sponsors (1)
Lead Sponsor Collaborator
University of Salamanca

Country where clinical trial is conducted

Spain, 

Outcome
Type Measure Description Time frame Safety issue
Primary Near Infrared Spectroscopy (NIRS) NIRS power 15 minutes per patients
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