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

U

University of Salamanca

Status

Terminated

Conditions

Abdominal Muscles

Treatments

Other: Vojta Therapy

Study type

Interventional

Funder types

Other

Identifiers

NCT05785962
ElectroVojta

Details and patient eligibility

About

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.

Enrollment

50 patients

Sex

All

Ages

18 to 80 years old

Volunteers

Accepts Healthy Volunteers

Inclusion and exclusion 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.

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.
  • Fever

Trial design

Primary purpose

Treatment

Allocation

Non-Randomized

Interventional model

Parallel Assignment

Masking

Double Blind

50 participants in 2 patient groups

Intervention group for people with brain damage
Experimental group
Description:
Other: Vojta The subject will be placed on a stretcher with the torso uncovered. Once the adhesive electrodes have been placed in the different recording areas on the anterior part of the trunk, a recording of the activity at rest will begin, two minutes of stimulation (digital pressure), one minute of rest, two minutes of stimulation in the contralateral side and, finally, one minute of rest. 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.
Treatment:
Other: Vojta Therapy
Intervention group for people without brain damage
Experimental group
Description:
Other: Vojta The subject will be placed on a stretcher with the torso uncovered. Once the adhesive electrodes have been placed in the different recording areas on the anterior part of the trunk, a recording of the activity at rest will begin, two minutes of stimulation (digital pressure), one minute of rest, two minutes of stimulation in the contralateral side and, finally, one minute of rest. 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.
Treatment:
Other: Vojta Therapy

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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