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Electromyographic Control of the Response in the Application of Vojta Therapy in People With Brain Injury.

Electromyographic Control of the Response in the Application of Vojta Therapy in People With Brain Injury.

Status
Terminated
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05785962
Acronym
ElectroVojta
Enrollment
50
Registered
2023-03-27
Start date
2024-09-01
Completion date
2025-06-25
Last updated
2025-10-07

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Abdominal Muscles

Brief summary

A non-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 will be to determine the feasibility of the standardized intervention protocol on the stabilizing muscles of the trunk (external oblique and internal oblique) before, during and after the application of Vojta Therapy, and to know the effects produced on the Musculature studied after performing the intervention.

Interventions

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.

Sponsors

University of Salamanca
Lead SponsorOTHER

Study design

Allocation
NON_RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE (Investigator, Outcomes Assessor)

Intervention model description

Subjects in each group will be matched by age and sex.

Eligibility

Sex/Gender
ALL
Age
18 Years to 80 Years
Healthy volunteers
Yes

Inclusion criteria

Brain injury group Inclusion Criteria : * Over 18 and under 80 years of age * Persons with a medical diagnosis of brain damage secondary to stroke * Have preserved the ability to walk, even with some type of orthopedic some type of orthopedic aid,

Exclusion criteria

* Over 80 years * Healthy people Group without brain damage Inclusion Criteria : * Over 18 and under 80 years of age * Healthy people * Full cognitive capacity.

Design outcomes

Primary

MeasureTime frameDescription
Electromyographic activity in abdominal musclesChange from Baseline electromyographic activity at 10 minutes.The electromyographic activity of internal and external obliques in nanovolts will be collected before, during and after the intervention. Acquired signals are sampled at 1 KHz and filtered with a 60 Hz high pass digital filter to reject signals of non-muscular origin. The degree of muscle activation measured in micro volts (uV) will be recorded.

Secondary

MeasureTime frameDescription
Date of birthBaselineIt will be registered at the beginning of the study in order to calculate the age of the participant.
SexBaselineIt will be registered at the beginning of the study.
HeightBaselineIt will be registered at the beginning of the study in centimeters.
WeightBaselineIt will be registered at the beginning of the study in centimeters.

Countries

Spain

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026